EFA6 in Axon Regeneration, as a Microtubule Regulator and as a Guanine Nucleotide Exchange Factor.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
26 05 2021
Historique:
received: 27 04 2021
revised: 23 05 2021
accepted: 24 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 3 11 2021
Statut: epublish

Résumé

Axon regeneration after injury is a conserved biological process that involves a large number of molecular pathways, including rapid calcium influx at injury sites, retrograde injury signaling, epigenetic transition, transcriptional reprogramming, polarized transport, and cytoskeleton reorganization. Despite the numerous efforts devoted to understanding the underlying cellular and molecular mechanisms of axon regeneration, the search continues for effective target molecules for improving axon regeneration. Although there have been significant historical efforts towards characterizing pro-regenerative factors involved in axon regeneration, the pursuit of intrinsic inhibitors is relatively recent. EFA6 (exchange factor for ARF6) has been demonstrated to inhibit axon regeneration in different organisms. EFA6 inhibition could be a promising therapeutic strategy to promote axon regeneration and functional recovery after axon injury. This review summarizes the inhibitory role on axon regeneration through regulating microtubule dynamics and through affecting ARF6 (ADP-ribosylation factor 6) GTPase-mediated integrin transport.

Identifiants

pubmed: 34073530
pii: cells10061325
doi: 10.3390/cells10061325
pmc: PMC8226579
pii:
doi:

Substances chimiques

ADP-Ribosylation Factor 6 0
Guanine Nucleotide Exchange Factors 0
ADP-Ribosylation Factors EC 3.6.5.2
ARF6 protein, human EC 3.6.5.2

Types de publication

Journal Article Research Support, N.I.H., Extramural Review Retracted Publication

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIH HHS
ID : 1R01AG070214-01
Pays : United States

Commentaires et corrections

Type : RetractionIn

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Auteurs

Gilberto Gonzalez (G)

Barshop Institute for Longevity and Aging Studies, Department of Cell Systems and Anatomy, UT Health San Antonio, San Antonio, TX 78229, USA.

Lizhen Chen (L)

Barshop Institute for Longevity and Aging Studies, Department of Cell Systems and Anatomy, UT Health San Antonio, San Antonio, TX 78229, USA.

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