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dc.contributor.authorChen, B
dc.contributor.authorHu, R
dc.contributor.authorMin, Q
dc.contributor.authorLi, Y
dc.contributor.authorParkinson, DB
dc.contributor.authorDun, X-P
dc.date.accessioned2020-08-04T07:56:11Z
dc.date.available2020-08-04T07:56:11Z
dc.date.issued2020-08-04
dc.identifier.issn1662-5102
dc.identifier.issn1662-5102
dc.identifier.otherARTN 237
dc.identifier.urihttp://hdl.handle.net/10026.1/16126
dc.description.abstract

The fibroblast growth factor (FGF) family polypeptides play key roles in promoting tissue regeneration and repair. FGF5 is strongly up-regulated in Schwann cells of the peripheral nervous system following injury; however, a role for FGF5 in peripheral nerve regeneration has not been shown up to now. In this report, we examined the expression of FGF5 and its receptors FGFR1-4 in Schwann cells of the mouse sciatic nerve following injury, and then measured the effects of FGF5 treatment upon cultured primary rat Schwann cells. By microarray and mRNA sequencing data analysis, RT-PCR, qPCR, western blotting and immunostaining, we show that FGF5 is highly up-regulated in Schwann cells of the mouse distal sciatic nerve following injury, and FGFR1 and FGFR2 are highly expressed in Schwann cells of the peripheral nerve both before and following injury. Using cultured primary rat Schwann cells, we show that FGF5 inhibits ERK1/2 MAP kinase activity but promotes rapid Schwann cell migration and adhesion via the upregulation of N-cadherin. Thus, FGF5 is an autocrine regulator of Schwann cells to regulate Schwann cell migration and adhesion.

dc.format.extent237-
dc.format.mediumElectronic-eCollection
dc.languageeng
dc.language.isoen
dc.publisherFrontiers Media SA
dc.subjectFGF5
dc.subjectreceptors
dc.subjectperipheral nerve injury
dc.subjectSchwann cell
dc.subjectmigration
dc.subjectadhesion
dc.subjectN-cadherin
dc.titleFGF5 Regulates Schwann Cell Migration and Adhesion
dc.typejournal-article
dc.typeArticle
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/32848626
plymouth.volume14
plymouth.publication-statusPublished online
plymouth.journalFrontiers in Cellular Neuroscience
dc.identifier.doi10.3389/fncel.2020.00237
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
dc.publisher.placeSwitzerland
dcterms.dateAccepted2020-07-06
dc.rights.embargodate2020-8-8
dc.identifier.eissn1662-5102
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.3389/fncel.2020.00237
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2020-08-04
rioxxterms.typeJournal Article/Review


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