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Cited by 52

The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.

Functional Genome-wide Screen Identifies Pathways Restricting Central Nervous System Axonal Regeneration

Sekine, Yuichi, Lin-Moore, Alexander, Chenette, Devon M., Wang, Xingxing, Jiang, Zhaoxin, Cafferty, William B., Hammarlund, Marc, Strittmatter, Stephen M.·2018·Cell Reports

Abstract

Axonal regrowth is crucial for recovery from CNS injury but is severely restricted in adult mammals. We used a genome-wide loss-of-function screen for factors limiting axonal regeneration from cerebral cortical neurons in vitro. Knockdown of 16,007 individual genes identified 580 significant phenotypes. These molecules share no significant overlap with those suggested by previous expression profiles. There is enrichment for genes in pathways related to transport, receptor binding, and cytokine signaling, including Socs4 and Ship2. Among transport-regulating proteins, Rab GTPases are prominent. In vivo assessment with C. elegans validates a cell-autonomous restriction of regeneration by Rab27. Mice lacking Rab27b show enhanced retinal ganglion cell axon regeneration after optic nerve crush and greater motor function and raphespinal sprouting after spinal cord trauma. Thus, a comprehensive functional screen reveals multiple pathways restricting axonal regeneration and neurological recovery after injury.

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Crossref · 10.1016/j.celrep.2018.03.058

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Metadata

Authors
Sekine, Y., Lin-Moore, A., Chenette, D. M., Wang, X., Jiang, Z., Cafferty, W. B., Hammarlund, M., & Strittmatter, S. M.
Venue
Cell Reports
Publisher
Elsevier BV
Published
2018-04
Volume
23
Issue
2
Pages
415-428
ISSN
2211-1247
Cited by
52
References
61
Language
en
Update notices
erratum (2018-07-03)
Licence
Funders
  • National Institutes of Health (R01NS098817, R35NS097283)
  • Dr. Ralph and Marian Falk Medical Research Trust

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