Show simple item record

dc.contributor.authorMindos, T
dc.contributor.authorDun, X-P
dc.contributor.authorNorth, K
dc.contributor.authorSchulz, A
dc.contributor.authorGray, B
dc.contributor.authorPan, D
dc.contributor.authorEdwards, P
dc.contributor.authorShivane, A
dc.contributor.authorMorrison, H
dc.contributor.authorParkinson, D
dc.date.accessioned2018-09-10T09:12:42Z
dc.date.available2018-09-10T09:12:42Z
dc.date.issued2017-01-30
dc.identifier.issn0021-9525
dc.identifier.issn1098-1136
dc.identifier.urihttp://hdl.handle.net/10026.1/12277
dc.description.abstract

Loss of the Merlin tumor suppressor and activation of the Hippo signaling pathway play major roles in the control of cell proliferation and tumorigenesis. We have identified completely novel roles for Merlin and the Hippo pathway effector Yes-associated protein (YAP) in the control of Schwann cell (SC) plasticity and peripheral nerve repair after injury. Injury to the peripheral nervous system (PNS) causes a dramatic shift in SC molecular phenotype and the generation of repair-competent SCs, which direct functional repair. We find that loss of Merlin in these cells causes a catastrophic failure of axonal regeneration and remyelination in the PNS. This effect is mediated by activation of YAP expression in Merlin-null SCs, and loss of YAP restores axonal regrowth and functional repair. This work identifies new mechanisms that control the regenerative potential of SCs and gives new insight into understanding the correct control of functional nerve repair in the PNS.

dc.format.extentE40-E41
dc.language.isoen
dc.publisherRockefeller University Press
dc.titleThe Merlin tumour suppressor controls the repair capacity of Schwann cells following injury by regulating Hippo pathway signalling
dc.typejournal-article
dc.typeMeeting Abstract
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000403071700060&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.volume65
plymouth.publication-statusPublished
plymouth.journalJournal of Cell Biology
dc.identifier.doi10.1083/jcb.201606052
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/Peninsula Medical School
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA03 Allied Health Professions, Dentistry, Nursing and Pharmacy
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
plymouth.organisational-group/Plymouth/Users by role/Researchers in ResearchFish submission
dcterms.dateAccepted2016-12-27
dc.identifier.eissn1098-1136
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1083/jcb.201606052
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2017-01-30
rioxxterms.typeJournal Article/Review


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV