---
APC_amount: 6081,83 EUR
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '17142'
abstract:
- lang: eng
  text: Despite the diverse genetic origins of autism spectrum disorders (ASDs), affected
    individuals share strikingly similar and correlated behavioural traits that include
    perceptual and sensory processing challenges. Notably, the severity of these sensory
    symptoms is often predictive of the expression of other autistic traits. However,
    the origin of these perceptual deficits remains largely elusive. Here, we show
    a recurrent impairment in visual threat perception that is similarly impaired
    in 3 independent mouse models of ASD with different molecular aetiologies. Interestingly,
    this deficit is associated with reduced avoidance of threatening environments—a
    nonperceptual trait. Focusing on a common cause of ASDs, the Setd5 gene mutation,
    we define the molecular mechanism. We show that the perceptual impairment is caused
    by a potassium channel (Kv1)-mediated hypoexcitability in a subcortical node essential
    for the initiation of escape responses, the dorsal periaqueductal grey (dPAG).
    Targeted pharmacological Kv1 blockade rescued both perceptual and place avoidance
    deficits, causally linking seemingly unrelated trait deficits to the dPAG. Furthermore,
    we show that different molecular mechanisms converge on similar behavioural phenotypes
    by demonstrating that the autism models Cul3 and Ptchd1, despite having similar
    behavioural phenotypes, differ in their functional and molecular alteration. Our
    findings reveal a link between rapid perception controlled by subcortical pathways
    and appropriate learned interactions with the environment and define a nondevelopmental
    source of such deficits in ASD.
acknowledgement: 'This work was supported by a European Research Council Starting
  Grant 756502 (MJ). '
article_number: e3002668
article_processing_charge: Yes
article_type: original
author:
- first_name: Laura
  full_name: Burnett, Laura
  id: 3B717F68-F248-11E8-B48F-1D18A9856A87
  last_name: Burnett
  orcid: 0000-0002-8937-410X
- first_name: Peter
  full_name: Koppensteiner, Peter
  id: 3B8B25A8-F248-11E8-B48F-1D18A9856A87
  last_name: Koppensteiner
  orcid: 0000-0002-3509-1948
- first_name: Olga
  full_name: Symonova, Olga
  id: 3C0C7BC6-F248-11E8-B48F-1D18A9856A87
  last_name: Symonova
  orcid: 0000-0003-2012-9947
- first_name: Tomas
  full_name: Masson, Tomas
  id: 93ac43e8-8599-11eb-9b86-f6efb0a4c207
  last_name: Masson
  orcid: 0000-0002-2634-6283
- first_name: Tomas A
  full_name: Vega Zuniga, Tomas A
  id: 2E7C4E78-F248-11E8-B48F-1D18A9856A87
  last_name: Vega Zuniga
- first_name: Ximena
  full_name: Contreras, Ximena
  id: 475990FE-F248-11E8-B48F-1D18A9856A87
  last_name: Contreras
- first_name: Thomas
  full_name: Rülicke, Thomas
  last_name: Rülicke
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Gaia
  full_name: Novarino, Gaia
  id: 3E57A680-F248-11E8-B48F-1D18A9856A87
  last_name: Novarino
  orcid: 0000-0002-7673-7178
- first_name: Maximilian A
  full_name: Jösch, Maximilian A
  id: 2BD278E6-F248-11E8-B48F-1D18A9856A87
  last_name: Jösch
  orcid: 0000-0002-3937-1330
citation:
  ama: Burnett L, Koppensteiner P, Symonova O, et al. Shared behavioural impairments
    in visual perception and place avoidance across different autism models are driven
    by periaqueductal grey hypoexcitability in Setd5 haploinsufficient mice. <i>PLoS
    Biology</i>. 2024;22. doi:<a href="https://doi.org/10.1371/journal.pbio.3002668">10.1371/journal.pbio.3002668</a>
  apa: Burnett, L., Koppensteiner, P., Symonova, O., Masson, T., Vega Zuniga, T. A.,
    Contreras, X., … Jösch, M. A. (2024). Shared behavioural impairments in visual
    perception and place avoidance across different autism models are driven by periaqueductal
    grey hypoexcitability in Setd5 haploinsufficient mice. <i>PLoS Biology</i>. Public
    Library of Science. <a href="https://doi.org/10.1371/journal.pbio.3002668">https://doi.org/10.1371/journal.pbio.3002668</a>
  chicago: Burnett, Laura, Peter Koppensteiner, Olga Symonova, Tomas Masson, Tomas
    A Vega Zuniga, Ximena Contreras, Thomas Rülicke, Ryuichi Shigemoto, Gaia Novarino,
    and Maximilian A Jösch. “Shared Behavioural Impairments in Visual Perception and
    Place Avoidance across Different Autism Models Are Driven by Periaqueductal Grey
    Hypoexcitability in Setd5 Haploinsufficient Mice.” <i>PLoS Biology</i>. Public
    Library of Science, 2024. <a href="https://doi.org/10.1371/journal.pbio.3002668">https://doi.org/10.1371/journal.pbio.3002668</a>.
  ieee: L. Burnett <i>et al.</i>, “Shared behavioural impairments in visual perception
    and place avoidance across different autism models are driven by periaqueductal
    grey hypoexcitability in Setd5 haploinsufficient mice,” <i>PLoS Biology</i>, vol.
    22. Public Library of Science, 2024.
  ista: Burnett L, Koppensteiner P, Symonova O, Masson T, Vega Zuniga TA, Contreras
    X, Rülicke T, Shigemoto R, Novarino G, Jösch MA. 2024. Shared behavioural impairments
    in visual perception and place avoidance across different autism models are driven
    by periaqueductal grey hypoexcitability in Setd5 haploinsufficient mice. PLoS
    Biology. 22, e3002668.
  mla: Burnett, Laura, et al. “Shared Behavioural Impairments in Visual Perception
    and Place Avoidance across Different Autism Models Are Driven by Periaqueductal
    Grey Hypoexcitability in Setd5 Haploinsufficient Mice.” <i>PLoS Biology</i>, vol.
    22, e3002668, Public Library of Science, 2024, doi:<a href="https://doi.org/10.1371/journal.pbio.3002668">10.1371/journal.pbio.3002668</a>.
  short: L. Burnett, P. Koppensteiner, O. Symonova, T. Masson, T.A. Vega Zuniga, X.
    Contreras, T. Rülicke, R. Shigemoto, G. Novarino, M.A. Jösch, PLoS Biology 22
    (2024).
corr_author: '1'
date_created: 2024-06-16T22:01:05Z
date_published: 2024-06-10T00:00:00Z
date_updated: 2025-09-08T07:57:11Z
day: '10'
ddc:
- '570'
department:
- _id: RySh
- _id: GaNo
- _id: MaJö
doi: 10.1371/journal.pbio.3002668
ec_funded: 1
external_id:
  isi:
  - '001246176800003'
  pmid:
  - '38857283'
file:
- access_level: open_access
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  content_type: application/pdf
  creator: dernst
  date_created: 2025-01-09T10:39:41Z
  date_updated: 2025-01-09T10:39:41Z
  file_id: '18805'
  file_name: 2024_PloS_Burnett.pdf
  file_size: 4016568
  relation: main_file
  success: 1
file_date_updated: 2025-01-09T10:39:41Z
has_accepted_license: '1'
intvolume: '        22'
isi: 1
language:
- iso: eng
license: https://creativecommons.org/licenses/by/4.0/
month: '06'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 2634E9D2-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '756502'
  name: Circuits of Visual Attention
publication: PLoS Biology
publication_identifier:
  eissn:
  - 1545-7885
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  link:
  - relation: software
    url: https://doi.org/10.5281/zenodo.11130587
  record:
  - id: '15385'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Shared behavioural impairments in visual perception and place avoidance across
  different autism models are driven by periaqueductal grey hypoexcitability in Setd5
  haploinsufficient mice
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 22
year: '2024'
...
---
APC_amount: 6248,82 EUR
DOAJ_listed: '1'
OA_place: publisher
OA_type: gold
_id: '18603'
abstract:
- lang: eng
  text: It is widely believed that information storage in neuronal circuits involves
    nanoscopic structural changes at synapses, resulting in the formation of synaptic
    engrams. However, direct evidence for this hypothesis is lacking. To test this
    conjecture, we combined chemical potentiation, functional analysis by paired pre-postsynaptic
    recordings, and structural analysis by electron microscopy (EM) and freeze-fracture
    replica labeling (FRL) at the rodent hippocampal mossy fiber synapse, a key synapse
    in the trisynaptic circuit of the hippocampus. Biophysical analysis of synaptic
    transmission revealed that forskolin-induced chemical potentiation increased the
    readily releasable vesicle pool size and vesicular release probability by 146%
    and 49%, respectively. Structural analysis of mossy fiber synapses by EM and FRL
    demonstrated an increase in the number of vesicles close to the plasma membrane
    and the number of clusters of the priming protein Munc13-1, indicating an increase
    in the number of both docked and primed vesicles. Furthermore, FRL analysis revealed
    a significant reduction of the distance between Munc13-1 and CaV2.1 Ca2+ channels,
    suggesting reconfiguration of the channel-vesicle coupling nanotopography. Our
    results indicate that presynaptic plasticity is associated with structural reorganization
    of active zones. We propose that changes in potential nanoscopic organization
    at synaptic vesicle release sites may be correlates of learning and memory at
    a plastic central synapse.
acknowledged_ssus:
- _id: EM-Fac
- _id: PreCl
acknowledgement: "We thank Carolina Borges-Merjane, Jing-Jing Chen, Katharina Lichter,
  and Samuel Young for critically reading the manuscript; the Electron Microscopy
  Facility of ISTA, in particular Vanessa Zheden, for extensive support, advice, and
  experimental assistance; the Preclinical Facility of ISTA, in particular Victoria
  Wimmer and Michael Schunn, for experimental assistance; Florian Marr and Christina
  Altmutter for technical support; Alois Schlögl for help with analysis; and Eleftheria
  Kralli-Beller for manuscript editing. We also thank Cordelia Imig for providing
  Munc13-1cKO-Munc13-2/3(−/−) mutant mice. Part of the work has been published in
  O.K.’s thesis in partial fulfillment of the requirements for the degree of Doctor
  of Philosophy.\r\nThis project received funding from the European Research Council
  and European Union’s Horizon 2020 research and innovation programme (ERC 692692
  to P.J.; https://cordis.europa.eu/project/id/692692/de) and from the Fond zur Förderung
  der Wissenschaftlichen Forschung (Z312-B27 Wittgenstein award to P.J., https://www.fwf.ac.at/en/funding/portfolio/projects/fwf-wittgenstein-award;
  W1205-B09 and P36232-B to P.J., https://www.fwf.ac.at/en/funding; I6166-B to R.S.;
  https://www.fwf.ac.at/en/funding). The funders had no role in study design, data
  collection and analysis, decision to publish, or preparation of the manuscript."
article_number: e3002879
article_processing_charge: Yes
article_type: original
author:
- first_name: Olena
  full_name: Kim, Olena
  id: 3F8ABDDA-F248-11E8-B48F-1D18A9856A87
  last_name: Kim
  orcid: 0000-0003-2344-1039
- first_name: Yuji
  full_name: Okamoto, Yuji
  id: 3337E116-F248-11E8-B48F-1D18A9856A87
  last_name: Okamoto
  orcid: 0000-0003-0408-6094
- first_name: Walter
  full_name: Kaufmann, Walter
  id: 3F99E422-F248-11E8-B48F-1D18A9856A87
  last_name: Kaufmann
  orcid: 0000-0001-9735-5315
- first_name: Nils
  full_name: Brose, Nils
  last_name: Brose
- first_name: Ryuichi
  full_name: Shigemoto, Ryuichi
  id: 499F3ABC-F248-11E8-B48F-1D18A9856A87
  last_name: Shigemoto
  orcid: 0000-0001-8761-9444
- first_name: Peter M
  full_name: Jonas, Peter M
  id: 353C1B58-F248-11E8-B48F-1D18A9856A87
  last_name: Jonas
  orcid: 0000-0001-5001-4804
citation:
  ama: Kim O, Okamoto Y, Kaufmann W, Brose N, Shigemoto R, Jonas PM. Presynaptic cAMP-PKA-mediated
    potentiation induces reconfiguration of synaptic vesicle pools and channel-vesicle
    coupling at hippocampal mossy fiber boutons. <i>PLoS Biology</i>. 2024;22(11).
    doi:<a href="https://doi.org/10.1371/journal.pbio.3002879">10.1371/journal.pbio.3002879</a>
  apa: Kim, O., Okamoto, Y., Kaufmann, W., Brose, N., Shigemoto, R., &#38; Jonas,
    P. M. (2024). Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration
    of synaptic vesicle pools and channel-vesicle coupling at hippocampal mossy fiber
    boutons. <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.3002879">https://doi.org/10.1371/journal.pbio.3002879</a>
  chicago: Kim, Olena, Yuji Okamoto, Walter Kaufmann, Nils Brose, Ryuichi Shigemoto,
    and Peter M Jonas. “Presynaptic CAMP-PKA-Mediated Potentiation Induces Reconfiguration
    of Synaptic Vesicle Pools and Channel-Vesicle Coupling at Hippocampal Mossy Fiber
    Boutons.” <i>PLoS Biology</i>. Public Library of Science, 2024. <a href="https://doi.org/10.1371/journal.pbio.3002879">https://doi.org/10.1371/journal.pbio.3002879</a>.
  ieee: O. Kim, Y. Okamoto, W. Kaufmann, N. Brose, R. Shigemoto, and P. M. Jonas,
    “Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic
    vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons,”
    <i>PLoS Biology</i>, vol. 22, no. 11. Public Library of Science, 2024.
  ista: Kim O, Okamoto Y, Kaufmann W, Brose N, Shigemoto R, Jonas PM. 2024. Presynaptic
    cAMP-PKA-mediated potentiation induces reconfiguration of synaptic vesicle pools
    and channel-vesicle coupling at hippocampal mossy fiber boutons. PLoS Biology.
    22(11), e3002879.
  mla: Kim, Olena, et al. “Presynaptic CAMP-PKA-Mediated Potentiation Induces Reconfiguration
    of Synaptic Vesicle Pools and Channel-Vesicle Coupling at Hippocampal Mossy Fiber
    Boutons.” <i>PLoS Biology</i>, vol. 22, no. 11, e3002879, Public Library of Science,
    2024, doi:<a href="https://doi.org/10.1371/journal.pbio.3002879">10.1371/journal.pbio.3002879</a>.
  short: O. Kim, Y. Okamoto, W. Kaufmann, N. Brose, R. Shigemoto, P.M. Jonas, PLoS
    Biology 22 (2024).
corr_author: '1'
date_created: 2024-12-01T23:01:54Z
date_published: 2024-11-18T00:00:00Z
date_updated: 2026-04-16T12:20:34Z
day: '18'
ddc:
- '570'
department:
- _id: PeJo
- _id: EM-Fac
- _id: RySh
doi: 10.1371/journal.pbio.3002879
ec_funded: 1
external_id:
  isi:
  - '001358568700003'
  pmid:
  - '39556620'
file:
- access_level: open_access
  checksum: 7de2dcb50deb65dde05c80082bb85a82
  content_type: application/pdf
  creator: dernst
  date_created: 2024-12-03T08:56:53Z
  date_updated: 2024-12-03T08:56:53Z
  file_id: '18608'
  file_name: 2024_PloSBio_Kim.pdf
  file_size: 3057631
  relation: main_file
  success: 1
file_date_updated: 2024-12-03T08:56:53Z
has_accepted_license: '1'
intvolume: '        22'
isi: 1
issue: '11'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
pmid: 1
project:
- _id: 25B7EB9E-B435-11E9-9278-68D0E5697425
  call_identifier: H2020
  grant_number: '692692'
  name: Biophysics and circuit function of a giant cortical glutamatergic synapse
- _id: 25C5A090-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: Z00312
  name: Synaptic communication in neuronal microcircuits
- _id: bd88be38-d553-11ed-ba76-81d5a70a6ef5
  grant_number: P36232
  name: Mechanisms of GABA release in hippocampal circuits
- _id: b1b85715-d554-11ed-a5ad-84a07fc9f18e
  grant_number: I06166
  name: Structural & functional basis of presynaptic plasticity
- _id: 25C3DBB6-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: W01205
  name: Zellkommunikation in Gesundheit und Krankheit
- _id: 3AC91DDA-15DF-11EA-824D-93A3E7B544D1
  call_identifier: FWF
  name: FWF Open Access Fund
publication: PLoS Biology
publication_identifier:
  eissn:
  - 1545-7885
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  record:
  - id: '18296'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Presynaptic cAMP-PKA-mediated potentiation induces reconfiguration of synaptic
  vesicle pools and channel-vesicle coupling at hippocampal mossy fiber boutons
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 22
year: '2024'
...
---
_id: '10614'
abstract:
- lang: eng
  text: 'The infiltration of immune cells into tissues underlies the establishment
    of tissue-resident macrophages and responses to infections and tumors. Yet the
    mechanisms immune cells utilize to negotiate tissue barriers in living organisms
    are not well understood, and a role for cortical actin has not been examined.
    Here, we find that the tissue invasion of Drosophila macrophages, also known as
    plasmatocytes or hemocytes, utilizes enhanced cortical F-actin levels stimulated
    by the Drosophila member of the fos proto oncogene transcription factor family
    (Dfos, Kayak). RNA sequencing analysis and live imaging show that Dfos enhances
    F-actin levels around the entire macrophage surface by increasing mRNA levels
    of the membrane spanning molecular scaffold tetraspanin TM4SF, and the actin cross-linking
    filamin Cheerio, which are themselves required for invasion. Both the filamin
    and the tetraspanin enhance the cortical activity of Rho1 and the formin Diaphanous
    and thus the assembly of cortical actin, which is a critical function since expressing
    a dominant active form of Diaphanous can rescue the Dfos macrophage invasion defect.
    In vivo imaging shows that Dfos enhances the efficiency of the initial phases
    of macrophage tissue entry. Genetic evidence argues that this Dfos-induced program
    in macrophages counteracts the constraint produced by the tension of surrounding
    tissues and buffers the properties of the macrophage nucleus from affecting tissue
    entry. We thus identify strengthening the cortical actin cytoskeleton through
    Dfos as a key process allowing efficient forward movement of an immune cell into
    surrounding tissues. '
acknowledged_ssus:
- _id: LifeSc
acknowledgement: 'We thank the following for their contributions: Plasmids were supplied
  by the Drosophila Genomics Resource Center (NIH 2P40OD010949-10A1); fly stocks were
  provided by K. Brueckner, B. Stramer, M. Uhlirova, O. Schuldiner, the Bloomington
  Drosophila Stock Center (NIH P40OD018537) and the Vienna Drosophila Resource Center,
  FlyBase for essential genomic information, and the BDGP in situ database for data.
  For antibodies, we thank the Developmental Studies Hybridoma Bank, which was created
  by the Eunice Kennedy Shriver National Institute of Child Health and Human Development
  of the NIH and is maintained at the University of Iowa, as well as J. Zeitlinger
  for her generous gift of Dfos antibody. We thank the Vienna BioCenter Core Facilities
  for RNA sequencing and analysis and the Life Scientific Service Units at IST Austria
  for technical support and assistance with microscopy and FACS analysis. We thank
  C. P. Heisenberg, P. Martin, M. Sixt, and Siekhaus group members for discussions
  and T. Hurd, A. Ratheesh, and P. Rangan for comments on the manuscript.'
article_processing_charge: No
article_type: original
author:
- first_name: Vera
  full_name: Belyaeva, Vera
  id: 47F080FE-F248-11E8-B48F-1D18A9856A87
  last_name: Belyaeva
- first_name: Stephanie
  full_name: Wachner, Stephanie
  id: 2A95E7B0-F248-11E8-B48F-1D18A9856A87
  last_name: Wachner
- first_name: Attila
  full_name: György, Attila
  id: 3BCEDBE0-F248-11E8-B48F-1D18A9856A87
  last_name: György
  orcid: 0000-0002-1819-198X
- first_name: Shamsi
  full_name: Emtenani, Shamsi
  id: 49D32318-F248-11E8-B48F-1D18A9856A87
  last_name: Emtenani
  orcid: 0000-0001-6981-6938
- first_name: Igor
  full_name: Gridchyn, Igor
  id: 4B60654C-F248-11E8-B48F-1D18A9856A87
  last_name: Gridchyn
  orcid: 0000-0002-1807-1929
- first_name: Maria
  full_name: Akhmanova, Maria
  id: 3425EC26-F248-11E8-B48F-1D18A9856A87
  last_name: Akhmanova
  orcid: 0000-0003-1522-3162
- first_name: M
  full_name: Linder, M
  last_name: Linder
- first_name: Marko
  full_name: Roblek, Marko
  id: 3047D808-F248-11E8-B48F-1D18A9856A87
  last_name: Roblek
  orcid: 0000-0001-9588-1389
- first_name: M
  full_name: Sibilia, M
  last_name: Sibilia
- first_name: Daria E
  full_name: Siekhaus, Daria E
  id: 3D224B9E-F248-11E8-B48F-1D18A9856A87
  last_name: Siekhaus
  orcid: 0000-0001-8323-8353
citation:
  ama: Belyaeva V, Wachner S, György A, et al. Fos regulates macrophage infiltration
    against surrounding tissue resistance by a cortical actin-based mechanism in Drosophila.
    <i>PLoS Biology</i>. 2022;20(1):e3001494. doi:<a href="https://doi.org/10.1371/journal.pbio.3001494">10.1371/journal.pbio.3001494</a>
  apa: Belyaeva, V., Wachner, S., György, A., Emtenani, S., Gridchyn, I., Akhmanova,
    M., … Siekhaus, D. E. (2022). Fos regulates macrophage infiltration against surrounding
    tissue resistance by a cortical actin-based mechanism in Drosophila. <i>PLoS Biology</i>.
    Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.3001494">https://doi.org/10.1371/journal.pbio.3001494</a>
  chicago: Belyaeva, Vera, Stephanie Wachner, Attila György, Shamsi Emtenani, Igor
    Gridchyn, Maria Akhmanova, M Linder, Marko Roblek, M Sibilia, and Daria E Siekhaus.
    “Fos Regulates Macrophage Infiltration against Surrounding Tissue Resistance by
    a Cortical Actin-Based Mechanism in Drosophila.” <i>PLoS Biology</i>. Public Library
    of Science, 2022. <a href="https://doi.org/10.1371/journal.pbio.3001494">https://doi.org/10.1371/journal.pbio.3001494</a>.
  ieee: V. Belyaeva <i>et al.</i>, “Fos regulates macrophage infiltration against
    surrounding tissue resistance by a cortical actin-based mechanism in Drosophila,”
    <i>PLoS Biology</i>, vol. 20, no. 1. Public Library of Science, p. e3001494, 2022.
  ista: Belyaeva V, Wachner S, György A, Emtenani S, Gridchyn I, Akhmanova M, Linder
    M, Roblek M, Sibilia M, Siekhaus DE. 2022. Fos regulates macrophage infiltration
    against surrounding tissue resistance by a cortical actin-based mechanism in Drosophila.
    PLoS Biology. 20(1), e3001494.
  mla: Belyaeva, Vera, et al. “Fos Regulates Macrophage Infiltration against Surrounding
    Tissue Resistance by a Cortical Actin-Based Mechanism in Drosophila.” <i>PLoS
    Biology</i>, vol. 20, no. 1, Public Library of Science, 2022, p. e3001494, doi:<a
    href="https://doi.org/10.1371/journal.pbio.3001494">10.1371/journal.pbio.3001494</a>.
  short: V. Belyaeva, S. Wachner, A. György, S. Emtenani, I. Gridchyn, M. Akhmanova,
    M. Linder, M. Roblek, M. Sibilia, D.E. Siekhaus, PLoS Biology 20 (2022) e3001494.
corr_author: '1'
date_created: 2022-01-12T10:18:17Z
date_published: 2022-01-06T00:00:00Z
date_updated: 2026-04-26T22:30:34Z
day: '06'
ddc:
- '570'
department:
- _id: DaSi
- _id: JoCs
doi: 10.1371/journal.pbio.3001494
ec_funded: 1
external_id:
  isi:
  - '000971223700001'
  pmid:
  - '34990456'
file:
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  checksum: f454212a5522a7818ba4b2892315c478
  content_type: application/pdf
  creator: cchlebak
  date_created: 2022-01-12T13:50:04Z
  date_updated: 2022-01-12T13:50:04Z
  file_id: '10615'
  file_name: 2022_PLOSBio_Belyaeva.pdf
  file_size: 5426932
  relation: main_file
  success: 1
file_date_updated: 2022-01-12T13:50:04Z
has_accepted_license: '1'
intvolume: '        20'
isi: 1
issue: '1'
language:
- iso: eng
month: '01'
oa: 1
oa_version: Published Version
page: e3001494
pmid: 1
project:
- _id: 253B6E48-B435-11E9-9278-68D0E5697425
  call_identifier: FWF
  grant_number: P29638
  name: The role of Drosophila TNF alpha in immune cell invasion
- _id: 26199CA4-B435-11E9-9278-68D0E5697425
  grant_number: '24800'
  name: Implications of a TGFÎ²/Dpp-activated subpopulation for Drosophila macrophage
    migration
- _id: 2536F660-B435-11E9-9278-68D0E5697425
  call_identifier: FP7
  grant_number: '334077'
  name: Investigating the role of transporters in invasive migration through junctions
publication: PLoS Biology
publication_identifier:
  eissn:
  - 1545-7885
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  link:
  - relation: earlier_version
    url: https://www.biorxiv.org/content/10.1101/2020.09.18.301481
  - description: News on the ISTA Website
    relation: press_release
    url: https://ista.ac.at/en/news/resisting-the-pressure/
  record:
  - id: '8557'
    relation: earlier_version
    status: public
  - id: '11193'
    relation: dissertation_contains
    status: public
scopus_import: '1'
status: public
title: Fos regulates macrophage infiltration against surrounding tissue resistance
  by a cortical actin-based mechanism in Drosophila
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 20
year: '2022'
...
---
_id: '10322'
abstract:
- lang: eng
  text: To survive elevated temperatures, ectotherms adjust the fluidity of membranes
    by fine-tuning lipid desaturation levels in a process previously described to
    be cell autonomous. We have discovered that, in Caenorhabditis elegans, neuronal
    heat shock factor 1 (HSF-1), the conserved master regulator of the heat shock
    response (HSR), causes extensive fat remodeling in peripheral tissues. These changes
    include a decrease in fat desaturase and acid lipase expression in the intestine
    and a global shift in the saturation levels of plasma membrane’s phospholipids.
    The observed remodeling of plasma membrane is in line with ectothermic adaptive
    responses and gives worms a cumulative advantage to warm temperatures. We have
    determined that at least 6 TAX-2/TAX-4 cyclic guanosine monophosphate (cGMP) gated
    channel expressing sensory neurons, and transforming growth factor ß (TGF-β)/bone
    morphogenetic protein (BMP) are required for signaling across tissues to modulate
    fat desaturation. We also find neuronal hsf-1 is not only sufficient but also
    partially necessary to control the fat remodeling response and for survival at
    warm temperatures. This is the first study to show that a thermostat-based mechanism
    can cell nonautonomously coordinate membrane saturation and composition across
    tissues in a multicellular animal.
acknowledgement: We dedicate this work to the memory of Michael J.O. Wakelam. We would
  like to acknowledge Michael Fasseas (Invermis, Magnitude Biosciences) for plasmid
  injections and Sunny Biotech for transgenics; Catalina Vallejos and John Marioni
  for statistical advice at the beginning of the work; Simon Walker, Imaging, Bioinformatics
  and Lipidomics Facilities at Babraham Institute for technical support; and Cindy
  Voisine, Michael Witting, Jon Houseley, Len Stephens, Carmen Nussbaum Krammer, Rebeca
  Aldunate, Patricija van Oosten-Hawle, Jean-Louis Bessereau, and Jane Alfred for
  feedback on the manuscript. We thank Andy Dillin, Atsushi Kuhara, Amy Walker, Andrew
  Leifer, Yun Zhang, and Michalis Barkoulas for reagents and Julie Ahringer, Anne
  Ferguson-Smith, and Anne Corcoran for support and helpful discussions. We also acknowledge
  Babraham Institute Facilities.
article_number: e3001431
article_processing_charge: No
article_type: original
author:
- first_name: Laetitia
  full_name: Chauve, Laetitia
  last_name: Chauve
- first_name: Francesca
  full_name: Hodge, Francesca
  last_name: Hodge
- first_name: Sharlene
  full_name: Murdoch, Sharlene
  last_name: Murdoch
- first_name: Fatemah
  full_name: Masoudzadeh, Fatemah
  last_name: Masoudzadeh
- first_name: Harry Jack
  full_name: Mann, Harry Jack
  last_name: Mann
- first_name: Andrea
  full_name: Lopez-Clavijo, Andrea
  last_name: Lopez-Clavijo
- first_name: Hanneke
  full_name: Okkenhaug, Hanneke
  last_name: Okkenhaug
- first_name: Greg
  full_name: West, Greg
  last_name: West
- first_name: Bebiana C.
  full_name: Sousa, Bebiana C.
  last_name: Sousa
- first_name: Anne
  full_name: Segonds-Pichon, Anne
  last_name: Segonds-Pichon
- first_name: Cheryl
  full_name: Li, Cheryl
  last_name: Li
- first_name: Steven
  full_name: Wingett, Steven
  last_name: Wingett
- first_name: Hermine
  full_name: Kienberger, Hermine
  last_name: Kienberger
- first_name: Karin
  full_name: Kleigrewe, Karin
  last_name: Kleigrewe
- first_name: Mario
  full_name: De Bono, Mario
  id: 4E3FF80E-F248-11E8-B48F-1D18A9856A87
  last_name: De Bono
  orcid: 0000-0001-8347-0443
- first_name: Michael
  full_name: Wakelam, Michael
  last_name: Wakelam
- first_name: Olivia
  full_name: Casanueva, Olivia
  last_name: Casanueva
citation:
  ama: Chauve L, Hodge F, Murdoch S, et al. Neuronal HSF-1 coordinates the propagation
    of fat desaturation across tissues to enable adaptation to high temperatures in
    C. elegans. <i>PLoS Biology</i>. 2021;19(11). doi:<a href="https://doi.org/10.1371/journal.pbio.3001431">10.1371/journal.pbio.3001431</a>
  apa: Chauve, L., Hodge, F., Murdoch, S., Masoudzadeh, F., Mann, H. J., Lopez-Clavijo,
    A., … Casanueva, O. (2021). Neuronal HSF-1 coordinates the propagation of fat
    desaturation across tissues to enable adaptation to high temperatures in C. elegans.
    <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.3001431">https://doi.org/10.1371/journal.pbio.3001431</a>
  chicago: Chauve, Laetitia, Francesca Hodge, Sharlene Murdoch, Fatemah Masoudzadeh,
    Harry Jack Mann, Andrea Lopez-Clavijo, Hanneke Okkenhaug, et al. “Neuronal HSF-1
    Coordinates the Propagation of Fat Desaturation across Tissues to Enable Adaptation
    to High Temperatures in C. Elegans.” <i>PLoS Biology</i>. Public Library of Science,
    2021. <a href="https://doi.org/10.1371/journal.pbio.3001431">https://doi.org/10.1371/journal.pbio.3001431</a>.
  ieee: L. Chauve <i>et al.</i>, “Neuronal HSF-1 coordinates the propagation of fat
    desaturation across tissues to enable adaptation to high temperatures in C. elegans,”
    <i>PLoS Biology</i>, vol. 19, no. 11. Public Library of Science, 2021.
  ista: Chauve L, Hodge F, Murdoch S, Masoudzadeh F, Mann HJ, Lopez-Clavijo A, Okkenhaug
    H, West G, Sousa BC, Segonds-Pichon A, Li C, Wingett S, Kienberger H, Kleigrewe
    K, de Bono M, Wakelam M, Casanueva O. 2021. Neuronal HSF-1 coordinates the propagation
    of fat desaturation across tissues to enable adaptation to high temperatures in
    C. elegans. PLoS Biology. 19(11), e3001431.
  mla: Chauve, Laetitia, et al. “Neuronal HSF-1 Coordinates the Propagation of Fat
    Desaturation across Tissues to Enable Adaptation to High Temperatures in C. Elegans.”
    <i>PLoS Biology</i>, vol. 19, no. 11, e3001431, Public Library of Science, 2021,
    doi:<a href="https://doi.org/10.1371/journal.pbio.3001431">10.1371/journal.pbio.3001431</a>.
  short: L. Chauve, F. Hodge, S. Murdoch, F. Masoudzadeh, H.J. Mann, A. Lopez-Clavijo,
    H. Okkenhaug, G. West, B.C. Sousa, A. Segonds-Pichon, C. Li, S. Wingett, H. Kienberger,
    K. Kleigrewe, M. de Bono, M. Wakelam, O. Casanueva, PLoS Biology 19 (2021).
date_created: 2021-11-21T23:01:28Z
date_published: 2021-11-01T00:00:00Z
date_updated: 2023-08-14T11:53:27Z
day: '01'
ddc:
- '570'
department:
- _id: MaDe
doi: 10.1371/journal.pbio.3001431
external_id:
  isi:
  - '000715818400001'
  pmid:
  - '34723964'
file:
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  creator: cchlebak
  date_created: 2021-11-22T09:34:03Z
  date_updated: 2021-11-22T09:34:03Z
  file_id: '10330'
  file_name: 2021_PLoSBio_Chauve.pdf
  file_size: 4069215
  relation: main_file
  success: 1
file_date_updated: 2021-11-22T09:34:03Z
has_accepted_license: '1'
intvolume: '        19'
isi: 1
issue: '11'
language:
- iso: eng
month: '11'
oa: 1
oa_version: Published Version
pmid: 1
publication: PLoS Biology
publication_identifier:
  eissn:
  - 1545-7885
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
related_material:
  record:
  - id: '13069'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Neuronal HSF-1 coordinates the propagation of fat desaturation across tissues
  to enable adaptation to high temperatures in C. elegans
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 4359f0d1-fa6c-11eb-b949-802e58b17ae8
volume: 19
year: '2021'
...
---
_id: '315'
abstract:
- lang: eng
  text: 'More than 100 years after Grigg’s influential analysis of species’ borders,
    the causes of limits to species’ ranges still represent a puzzle that has never
    been understood with clarity. The topic has become especially important recently
    as many scientists have become interested in the potential for species’ ranges
    to shift in response to climate change—and yet nearly all of those studies fail
    to recognise or incorporate evolutionary genetics in a way that relates to theoretical
    developments. I show that range margins can be understood based on just two measurable
    parameters: (i) the fitness cost of dispersal—a measure of environmental heterogeneity—and
    (ii) the strength of genetic drift, which reduces genetic diversity. Together,
    these two parameters define an ‘expansion threshold’: adaptation fails when genetic
    drift reduces genetic diversity below that required for adaptation to a heterogeneous
    environment. When the key parameters drop below this expansion threshold locally,
    a sharp range margin forms. When they drop below this threshold throughout the
    species’ range, adaptation collapses everywhere, resulting in either extinction
    or formation of a fragmented metapopulation. Because the effects of dispersal
    differ fundamentally with dimension, the second parameter—the strength of genetic
    drift—is qualitatively different compared to a linear habitat. In two-dimensional
    habitats, genetic drift becomes effectively independent of selection. It decreases
    with ‘neighbourhood size’—the number of individuals accessible by dispersal within
    one generation. Moreover, in contrast to earlier predictions, which neglected
    evolution of genetic variance and/or stochasticity in two dimensions, dispersal
    into small marginal populations aids adaptation. This is because the reduction
    of both genetic and demographic stochasticity has a stronger effect than the cost
    of dispersal through increased maladaptation. The expansion threshold thus provides
    a novel, theoretically justified, and testable prediction for formation of the
    range margin and collapse of the species’ range.'
article_number: e2005372
article_processing_charge: No
author:
- first_name: Jitka
  full_name: Polechova, Jitka
  id: 3BBFB084-F248-11E8-B48F-1D18A9856A87
  last_name: Polechova
  orcid: 0000-0003-0951-3112
citation:
  ama: Polechova J. Is the sky the limit? On the expansion threshold of a species’
    range. <i>PLoS Biology</i>. 2018;16(6). doi:<a href="https://doi.org/10.1371/journal.pbio.2005372">10.1371/journal.pbio.2005372</a>
  apa: Polechova, J. (2018). Is the sky the limit? On the expansion threshold of a
    species’ range. <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.2005372">https://doi.org/10.1371/journal.pbio.2005372</a>
  chicago: Polechova, Jitka. “Is the Sky the Limit? On the Expansion Threshold of
    a Species’ Range.” <i>PLoS Biology</i>. Public Library of Science, 2018. <a href="https://doi.org/10.1371/journal.pbio.2005372">https://doi.org/10.1371/journal.pbio.2005372</a>.
  ieee: J. Polechova, “Is the sky the limit? On the expansion threshold of a species’
    range,” <i>PLoS Biology</i>, vol. 16, no. 6. Public Library of Science, 2018.
  ista: Polechova J. 2018. Is the sky the limit? On the expansion threshold of a species’
    range. PLoS Biology. 16(6), e2005372.
  mla: Polechova, Jitka. “Is the Sky the Limit? On the Expansion Threshold of a Species’
    Range.” <i>PLoS Biology</i>, vol. 16, no. 6, e2005372, Public Library of Science,
    2018, doi:<a href="https://doi.org/10.1371/journal.pbio.2005372">10.1371/journal.pbio.2005372</a>.
  short: J. Polechova, PLoS Biology 16 (2018).
date_created: 2018-12-11T11:45:46Z
date_published: 2018-06-15T00:00:00Z
date_updated: 2025-07-10T11:52:27Z
day: '15'
ddc:
- '576'
department:
- _id: NiBa
doi: 10.1371/journal.pbio.2005372
file:
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  checksum: 908c52751bba30c55ed36789e5e4c84d
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  date_created: 2019-01-22T08:30:03Z
  date_updated: 2020-07-14T12:46:01Z
  file_id: '5870'
  file_name: 2017_PLOS_Polechova.pdf
  file_size: 6968201
  relation: main_file
file_date_updated: 2020-07-14T12:46:01Z
has_accepted_license: '1'
intvolume: '        16'
issue: '6'
language:
- iso: eng
month: '06'
oa: 1
oa_version: Published Version
publication: PLoS Biology
publication_identifier:
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
publist_id: '7550'
quality_controlled: '1'
related_material:
  record:
  - id: '9839'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Is the sky the limit? On the expansion threshold of a species’ range
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 16
year: '2018'
...
---
_id: '951'
abstract:
- lang: eng
  text: Dengue-suppressing Wolbachia strains are promising tools for arbovirus control,
    particularly as they have the potential to self-spread following local introductions.
    To test this, we followed the frequency of the transinfected Wolbachia strain
    wMel through Ae. aegypti in Cairns, Australia, following releases at 3 nonisolated
    locations within the city in early 2013. Spatial spread was analysed graphically
    using interpolation and by fitting a statistical model describing the position
    and width of the wave. For the larger 2 of the 3 releases (covering 0.97 km2 and
    0.52 km2), we observed slow but steady spatial spread, at about 100–200 m per
    year, roughly consistent with theoretical predictions. In contrast, the smallest
    release (0.11 km2) produced erratic temporal and spatial dynamics, with little
    evidence of spread after 2 years. This is consistent with the prediction concerning
    fitness-decreasing Wolbachia transinfections that a minimum release area is needed
    to achieve stable local establishment and spread in continuous habitats. Our graphical
    and likelihood analyses produced broadly consistent estimates of wave speed and
    wave width. Spread at all sites was spatially heterogeneous, suggesting that environmental
    heterogeneity will affect large-scale Wolbachia transformations of urban mosquito
    populations. The persistence and spread of Wolbachia in release areas meeting
    minimum area requirements indicates the promise of successful large-scale population
    transfo
article_number: e2001894
article_processing_charge: No
author:
- first_name: Tom
  full_name: Schmidt, Tom
  last_name: Schmidt
- first_name: Nicholas H
  full_name: Barton, Nicholas H
  id: 4880FE40-F248-11E8-B48F-1D18A9856A87
  last_name: Barton
  orcid: 0000-0002-8548-5240
- first_name: Gordana
  full_name: Rasic, Gordana
  last_name: Rasic
- first_name: Andrew
  full_name: Turley, Andrew
  last_name: Turley
- first_name: Brian
  full_name: Montgomery, Brian
  last_name: Montgomery
- first_name: Inaki
  full_name: Iturbe Ormaetxe, Inaki
  last_name: Iturbe Ormaetxe
- first_name: Peter
  full_name: Cook, Peter
  last_name: Cook
- first_name: Peter
  full_name: Ryan, Peter
  last_name: Ryan
- first_name: Scott
  full_name: Ritchie, Scott
  last_name: Ritchie
- first_name: Ary
  full_name: Hoffmann, Ary
  last_name: Hoffmann
- first_name: Scott
  full_name: O’Neill, Scott
  last_name: O’Neill
- first_name: Michael
  full_name: Turelli, Michael
  last_name: Turelli
citation:
  ama: Schmidt T, Barton NH, Rasic G, et al. Local introduction and heterogeneous
    spatial spread of dengue-suppressing Wolbachia through an urban population of
    Aedes Aegypti. <i>PLoS Biology</i>. 2017;15(5). doi:<a href="https://doi.org/10.1371/journal.pbio.2001894">10.1371/journal.pbio.2001894</a>
  apa: Schmidt, T., Barton, N. H., Rasic, G., Turley, A., Montgomery, B., Iturbe Ormaetxe,
    I., … Turelli, M. (2017). Local introduction and heterogeneous spatial spread
    of dengue-suppressing Wolbachia through an urban population of Aedes Aegypti.
    <i>PLoS Biology</i>. Public Library of Science. <a href="https://doi.org/10.1371/journal.pbio.2001894">https://doi.org/10.1371/journal.pbio.2001894</a>
  chicago: Schmidt, Tom, Nicholas H Barton, Gordana Rasic, Andrew Turley, Brian Montgomery,
    Inaki Iturbe Ormaetxe, Peter Cook, et al. “Local Introduction and Heterogeneous
    Spatial Spread of Dengue-Suppressing Wolbachia through an Urban Population of
    Aedes Aegypti.” <i>PLoS Biology</i>. Public Library of Science, 2017. <a href="https://doi.org/10.1371/journal.pbio.2001894">https://doi.org/10.1371/journal.pbio.2001894</a>.
  ieee: T. Schmidt <i>et al.</i>, “Local introduction and heterogeneous spatial spread
    of dengue-suppressing Wolbachia through an urban population of Aedes Aegypti,”
    <i>PLoS Biology</i>, vol. 15, no. 5. Public Library of Science, 2017.
  ista: Schmidt T, Barton NH, Rasic G, Turley A, Montgomery B, Iturbe Ormaetxe I,
    Cook P, Ryan P, Ritchie S, Hoffmann A, O’Neill S, Turelli M. 2017. Local introduction
    and heterogeneous spatial spread of dengue-suppressing Wolbachia through an urban
    population of Aedes Aegypti. PLoS Biology. 15(5), e2001894.
  mla: Schmidt, Tom, et al. “Local Introduction and Heterogeneous Spatial Spread of
    Dengue-Suppressing Wolbachia through an Urban Population of Aedes Aegypti.” <i>PLoS
    Biology</i>, vol. 15, no. 5, e2001894, Public Library of Science, 2017, doi:<a
    href="https://doi.org/10.1371/journal.pbio.2001894">10.1371/journal.pbio.2001894</a>.
  short: T. Schmidt, N.H. Barton, G. Rasic, A. Turley, B. Montgomery, I. Iturbe Ormaetxe,
    P. Cook, P. Ryan, S. Ritchie, A. Hoffmann, S. O’Neill, M. Turelli, PLoS Biology
    15 (2017).
date_created: 2018-12-11T11:49:22Z
date_published: 2017-05-30T00:00:00Z
date_updated: 2025-07-10T12:01:48Z
day: '30'
ddc:
- '576'
department:
- _id: NiBa
doi: 10.1371/journal.pbio.2001894
external_id:
  isi:
  - '000402520000012'
file:
- access_level: open_access
  checksum: 107d290bd1159ec77b734eb2824b01c8
  content_type: application/pdf
  creator: system
  date_created: 2018-12-12T10:08:30Z
  date_updated: 2020-07-14T12:48:16Z
  file_id: '4691'
  file_name: IST-2017-843-v1+1_journal.pbio.2001894.pdf
  file_size: 5541206
  relation: main_file
file_date_updated: 2020-07-14T12:48:16Z
has_accepted_license: '1'
intvolume: '        15'
isi: 1
issue: '5'
language:
- iso: eng
month: '05'
oa: 1
oa_version: Published Version
publication: PLoS Biology
publication_identifier:
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
publist_id: '6464'
pubrep_id: '843'
quality_controlled: '1'
related_material:
  record:
  - id: '9856'
    relation: research_data
    status: public
  - id: '9857'
    relation: research_data
    status: public
  - id: '9858'
    relation: research_data
    status: public
scopus_import: '1'
status: public
title: Local introduction and heterogeneous spatial spread of dengue-suppressing Wolbachia
  through an urban population of Aedes Aegypti
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 2DF688A6-F248-11E8-B48F-1D18A9856A87
volume: 15
year: '2017'
...
---
_id: '708'
abstract:
- lang: eng
  text: 'In the developing and adult brain, oligodendrocyte precursor cells (OPCs)
    are influenced by neuronal activity: they are involved in synaptic signaling with
    neurons, and their proliferation and differentiation into myelinating glia can
    be altered by transient changes in neuronal firing. An important question that
    has been unanswered is whether OPCs can discriminate different patterns of neuronal
    activity and respond to them in a distinct way. Here, we demonstrate in brain
    slices that the pattern of neuronal activity determines the functional changes
    triggered at synapses between axons and OPCs. Furthermore, we show that stimulation
    of the corpus callosum at different frequencies in vivo affects proliferation
    and differentiation of OPCs in a dissimilar way. Our findings suggest that neurons
    do not influence OPCs in “all-or-none” fashion but use their firing pattern to
    tune the response and behavior of these nonneuronal cells.'
article_number: e2001993
article_processing_charge: No
author:
- first_name: Balint
  full_name: Nagy, Balint
  id: 30F830CE-02D1-11E9-9BAA-DAF4881429F2
  last_name: Nagy
  orcid: 0000-0002-4002-4686
- first_name: Anahit
  full_name: Hovhannisyan, Anahit
  last_name: Hovhannisyan
- first_name: Ruxandra
  full_name: Barzan, Ruxandra
  last_name: Barzan
- first_name: Ting
  full_name: Chen, Ting
  last_name: Chen
- first_name: Maria
  full_name: Kukley, Maria
  last_name: Kukley
citation:
  ama: Nagy B, Hovhannisyan A, Barzan R, Chen T, Kukley M. Different patterns of neuronal
    activity trigger distinct responses of oligodendrocyte precursor cells in the
    corpus callosum. <i>PLoS Biology</i>. 2017;15(8). doi:<a href="https://doi.org/10.1371/journal.pbio.2001993">10.1371/journal.pbio.2001993</a>
  apa: Nagy, B., Hovhannisyan, A., Barzan, R., Chen, T., &#38; Kukley, M. (2017).
    Different patterns of neuronal activity trigger distinct responses of oligodendrocyte
    precursor cells in the corpus callosum. <i>PLoS Biology</i>. Public Library of
    Science. <a href="https://doi.org/10.1371/journal.pbio.2001993">https://doi.org/10.1371/journal.pbio.2001993</a>
  chicago: Nagy, Balint, Anahit Hovhannisyan, Ruxandra Barzan, Ting Chen, and Maria
    Kukley. “Different Patterns of Neuronal Activity Trigger Distinct Responses of
    Oligodendrocyte Precursor Cells in the Corpus Callosum.” <i>PLoS Biology</i>.
    Public Library of Science, 2017. <a href="https://doi.org/10.1371/journal.pbio.2001993">https://doi.org/10.1371/journal.pbio.2001993</a>.
  ieee: B. Nagy, A. Hovhannisyan, R. Barzan, T. Chen, and M. Kukley, “Different patterns
    of neuronal activity trigger distinct responses of oligodendrocyte precursor cells
    in the corpus callosum,” <i>PLoS Biology</i>, vol. 15, no. 8. Public Library of
    Science, 2017.
  ista: Nagy B, Hovhannisyan A, Barzan R, Chen T, Kukley M. 2017. Different patterns
    of neuronal activity trigger distinct responses of oligodendrocyte precursor cells
    in the corpus callosum. PLoS Biology. 15(8), e2001993.
  mla: Nagy, Balint, et al. “Different Patterns of Neuronal Activity Trigger Distinct
    Responses of Oligodendrocyte Precursor Cells in the Corpus Callosum.” <i>PLoS
    Biology</i>, vol. 15, no. 8, e2001993, Public Library of Science, 2017, doi:<a
    href="https://doi.org/10.1371/journal.pbio.2001993">10.1371/journal.pbio.2001993</a>.
  short: B. Nagy, A. Hovhannisyan, R. Barzan, T. Chen, M. Kukley, PLoS Biology 15
    (2017).
corr_author: '1'
date_created: 2018-12-11T11:48:03Z
date_published: 2017-08-22T00:00:00Z
date_updated: 2025-09-10T11:05:19Z
day: '22'
ddc:
- '576'
- '610'
department:
- _id: SaSi
doi: 10.1371/journal.pbio.2001993
external_id:
  isi:
  - '000408756200005'
file:
- access_level: open_access
  checksum: 0c974f430682dc832ea7b27ab5a93124
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  creator: system
  date_created: 2018-12-12T10:15:35Z
  date_updated: 2020-07-14T12:47:49Z
  file_id: '5156'
  file_name: IST-2017-889-v1+1_journal.pbio.2001993.pdf
  file_size: 18155365
  relation: main_file
file_date_updated: 2020-07-14T12:47:49Z
has_accepted_license: '1'
intvolume: '        15'
isi: 1
issue: '8'
language:
- iso: eng
month: '08'
oa: 1
oa_version: Published Version
publication: PLoS Biology
publication_identifier:
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
publist_id: '6983'
pubrep_id: '889'
quality_controlled: '1'
scopus_import: '1'
status: public
title: Different patterns of neuronal activity trigger distinct responses of oligodendrocyte
  precursor cells in the corpus callosum
tmp:
  image: /images/cc_by.png
  legal_code_url: https://creativecommons.org/licenses/by/4.0/legalcode
  name: Creative Commons Attribution 4.0 International Public License (CC-BY 4.0)
  short: CC BY (4.0)
type: journal_article
user_id: 317138e5-6ab7-11ef-aa6d-ffef3953e345
volume: 15
year: '2017'
...
---
_id: '9517'
abstract:
- lang: eng
  text: Multicellular eukaryotes produce small RNA molecules (approximately 21–24
    nucleotides) of two general types, microRNA (miRNA) and short interfering RNA
    (siRNA). They collectively function as sequence-specific guides to silence or
    regulate genes, transposons, and viruses and to modify chromatin and genome structure.
    Formation or activity of small RNAs requires factors belonging to gene families
    that encode DICER (or DICER-LIKE [DCL]) and ARGONAUTE proteins and, in the case
    of some siRNAs, RNA-dependent RNA polymerase (RDR) proteins. Unlike many animals,
    plants encode multiple DCL and RDR proteins. Using a series of insertion mutants
    of Arabidopsis thaliana, unique functions for three DCL proteins in miRNA (DCL1),
    endogenous siRNA (DCL3), and viral siRNA (DCL2) biogenesis were identified. One
    RDR protein (RDR2) was required for all endogenous siRNAs analyzed. The loss of
    endogenous siRNA in dcl3 and rdr2 mutants was associated with loss of heterochromatic
    marks and increased transcript accumulation at some loci. Defects in siRNA-generation
    activity in response to turnip crinkle virus in dcl2 mutant plants correlated
    with increased virus susceptibility. We conclude that proliferation and diversification
    of DCL and RDR genes during evolution of plants contributed to specialization
    of small RNA-directed pathways for development, chromatin structure, and defense.
article_processing_charge: No
article_type: original
author:
- first_name: Zhixin
  full_name: Xie, Zhixin
  last_name: Xie
- first_name: Lisa K.
  full_name: Johansen, Lisa K.
  last_name: Johansen
- first_name: Adam M.
  full_name: Gustafson, Adam M.
  last_name: Gustafson
- first_name: Kristin D.
  full_name: Kasschau, Kristin D.
  last_name: Kasschau
- first_name: 'Andrew D. '
  full_name: 'Lellis, Andrew D. '
  last_name: Lellis
- first_name: Daniel
  full_name: Zilberman, Daniel
  id: 6973db13-dd5f-11ea-814e-b3e5455e9ed1
  last_name: Zilberman
  orcid: 0000-0002-0123-8649
- first_name: Steven E.
  full_name: Jacobsen, Steven E.
  last_name: Jacobsen
- first_name: James C.
  full_name: Carrington, James C.
  last_name: Carrington
citation:
  ama: Xie Z, Johansen LK, Gustafson AM, et al. Genetic and functional diversification
    of small RNA pathways in plants. <i>PLoS Biology</i>. 2004;2(5):0642-0652. doi:<a
    href="https://doi.org/10.1371/journal.pbio.0020104">10.1371/journal.pbio.0020104</a>
  apa: Xie, Z., Johansen, L. K., Gustafson, A. M., Kasschau, K. D., Lellis, A. D.,
    Zilberman, D., … Carrington, J. C. (2004). Genetic and functional diversification
    of small RNA pathways in plants. <i>PLoS Biology</i>. Public Library of Science.
    <a href="https://doi.org/10.1371/journal.pbio.0020104">https://doi.org/10.1371/journal.pbio.0020104</a>
  chicago: Xie, Zhixin, Lisa K. Johansen, Adam M. Gustafson, Kristin D. Kasschau,
    Andrew D.  Lellis, Daniel Zilberman, Steven E. Jacobsen, and James C. Carrington.
    “Genetic and Functional Diversification of Small RNA Pathways in Plants.” <i>PLoS
    Biology</i>. Public Library of Science, 2004. <a href="https://doi.org/10.1371/journal.pbio.0020104">https://doi.org/10.1371/journal.pbio.0020104</a>.
  ieee: Z. Xie <i>et al.</i>, “Genetic and functional diversification of small RNA
    pathways in plants,” <i>PLoS Biology</i>, vol. 2, no. 5. Public Library of Science,
    pp. 0642–0652, 2004.
  ista: Xie Z, Johansen LK, Gustafson AM, Kasschau KD, Lellis AD, Zilberman D, Jacobsen
    SE, Carrington JC. 2004. Genetic and functional diversification of small RNA pathways
    in plants. PLoS Biology. 2(5), 0642–0652.
  mla: Xie, Zhixin, et al. “Genetic and Functional Diversification of Small RNA Pathways
    in Plants.” <i>PLoS Biology</i>, vol. 2, no. 5, Public Library of Science, 2004,
    pp. 0642–52, doi:<a href="https://doi.org/10.1371/journal.pbio.0020104">10.1371/journal.pbio.0020104</a>.
  short: Z. Xie, L.K. Johansen, A.M. Gustafson, K.D. Kasschau, A.D. Lellis, D. Zilberman,
    S.E. Jacobsen, J.C. Carrington, PLoS Biology 2 (2004) 0642–0652.
date_created: 2021-06-07T14:12:08Z
date_published: 2004-02-24T00:00:00Z
date_updated: 2021-12-14T08:43:57Z
day: '24'
department:
- _id: DaZi
doi: 10.1371/journal.pbio.0020104
extern: '1'
external_id:
  pmid:
  - '15024409'
intvolume: '         2'
issue: '5'
language:
- iso: eng
main_file_link:
- open_access: '1'
  url: https://doi.org/10.1371/journal.pbio.0020104
month: '02'
oa: 1
oa_version: Published Version
page: 0642-0652
pmid: 1
publication: PLoS Biology
publication_identifier:
  eissn:
  - 1545-7885
  issn:
  - 1544-9173
publication_status: published
publisher: Public Library of Science
quality_controlled: '1'
scopus_import: '1'
status: public
title: Genetic and functional diversification of small RNA pathways in plants
type: journal_article
user_id: 8b945eb4-e2f2-11eb-945a-df72226e66a9
volume: 2
year: '2004'
...
