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dc.creatorWang, Xue-Wei
dc.creatorLi, Qiao
dc.creatorLiu, Chang-Mei
dc.creatorHall, Philip A.
dc.creatorJiang, Jing-Jing
dc.creatorKatchis, Christopher D.
dc.creatorKang, Sehwa
dc.creatorDong, Bryan C.
dc.creatorLi, Shuxin
dc.creatorZhou, Feng-Quan
dc.date.accessioned2023-06-22T15:11:32Z
dc.date.available2023-06-22T15:11:32Z
dc.date.issued2018-09-04
dc.identifier.issn2211-1247
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/8727
dc.identifier.urihttp://hdl.handle.net/20.500.12613/8763
dc.description.abstractRNA-binding proteins Lin28a/b regulate cellular growth and tissue regeneration. Here, we investigated the role of Lin28 in the control of axon regeneration in postmitotic neurons. We find that Lin28a/b are both necessary and sufficient for supporting axon regeneration in mature sensory neurons through their regulatory partners, let-7 microRNAs (miRNAs). More importantly, overexpression of Lin28a in mature retinal ganglion cells (RGCs) produces robust and sustained optic nerve regeneration. Additionally, combined overexpression of Lin28a and downregulation of Pten in RGCs act additively to promote optic nerve regeneration, potentially by reducing the backward turning of regenerating RGC axons. Our findings not only reveal a vital role of Lin28 signaling in regulating mammalian axon regeneration but also identify a signaling pathway that can promote axon regeneration in the central nervous system (CNS).
dc.format.extent20 pages
dc.languageEnglish
dc.language.isoeng
dc.relation.ispartofFaculty/ Researcher Works
dc.relation.haspartCell Reports, Vol. 24, Iss. 10
dc.relation.isreferencedbyCell Press
dc.rightsAttribution-NonCommercial-NoDerivs CC BY-NC-ND
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectLin28
dc.subjectAxon regeneration
dc.subjectOptic nerve regeneration
dc.subjectReprogramming factor
dc.subjectLet-7
dc.subjectRNA binding protein
dc.subjectMicroRNA
dc.subjectSciatic nerve
dc.subjectDorsal root ganglion
dc.subjectRetinal ganglion cell
dc.titleLin28 Signaling Supports Mammalian PNS and CNS Axon Regeneration
dc.typeText
dc.type.genreJournal article
dc.contributor.groupShriners Hospital Pediatric Research Center (Temple University)
dc.description.departmentAnatomy and Cell Biology
dc.relation.doihttps://doi.org/10.1016/j.celrep.2018.07.105
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.description.schoolcollegeLewis Katz School of Medicine
dc.temple.creatorLi, Shuxin
refterms.dateFOA2023-06-22T15:11:32Z


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