Genre
Journal articleDate
2018-09-04Author
Wang, Xue-WeiLi, Qiao
Liu, Chang-Mei
Hall, Philip A.
Jiang, Jing-Jing
Katchis, Christopher D.
Kang, Sehwa
Dong, Bryan C.
Li, Shuxin
Zhou, Feng-Quan
Group
Shriners Hospital Pediatric Research Center (Temple University)Department
Anatomy and Cell BiologySubject
Lin28Axon regeneration
Optic nerve regeneration
Reprogramming factor
Let-7
RNA binding protein
MicroRNA
Sciatic nerve
Dorsal root ganglion
Retinal ganglion cell
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http://hdl.handle.net/20.500.12613/8763
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https://doi.org/10.1016/j.celrep.2018.07.105Abstract
RNA-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).Citation to related work
Cell PressHas part
Cell Reports, Vol. 24, Iss. 10ADA compliance
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http://dx.doi.org/10.34944/dspace/8727
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