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J Cell Biol DOI:10.1083/jcb.201705085

A neuroprotective agent that inactivates prodegenerative TrkA and preserves mitochondria.

Publication TypeJournal Article
Year of Publication2017
AuthorsFeinberg, K, Kolaj, A, Wu, C, Grinshtein, N, Krieger, JR, Moran, MF, Rubin, LL, Miller, FD, Kaplan, DR
JournalJ Cell Biol
Volume216
Issue11
Pages3655-3675
Date Published2017 Nov 06
ISSN1540-8140
Abstract

Axon degeneration is an early event and pathological in neurodegenerative conditions and nerve injuries. To discover agents that suppress neuronal death and axonal degeneration, we performed drug screens on primary rodent neurons and identified the pan-kinase inhibitor foretinib, which potently rescued sympathetic, sensory, and motor wt and SOD1 mutant neurons from trophic factor withdrawal-induced degeneration. By using primary sympathetic neurons grown in mass cultures and Campenot chambers, we show that foretinib protected neurons by suppressing both known degenerative pathways and a new pathway involving unliganded TrkA and transcriptional regulation of the proapoptotic BH3 family members BimEL, Harakiri,and Puma, culminating in preservation of mitochondria in the degenerative setting. Foretinib delayed chemotherapy-induced and Wallerian axonal degeneration in culture by preventing axotomy-induced local energy deficit and preserving mitochondria, and peripheral Wallerian degeneration in vivo. These findings identify a new axon degeneration pathway and a potentially clinically useful therapeutic drug.

DOI10.1083/jcb.201705085
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/28877995?dopt=Abstract

Alternate JournalJ. Cell Biol.
PubMed ID28877995
PubMed Central IDPMC5674898