Retrograde apoptotic signaling by the p75 neurotrophin receptor
Author(s) -
Amrita Pathak,
Bruce Carter
Publication year - 2017
Publication title -
neuronal signaling
Language(s) - English
Resource type - Journals
ISSN - 2059-6553
DOI - 10.1042/ns20160007
Subject(s) - neurotrophin , trk receptor , retrograde signaling , neuroscience , axon , receptor , low affinity nerve growth factor receptor , biology , neurodegeneration , signal transduction , soma , nervous system , microbiology and biotechnology , medicine , genetics , disease
Neurotrophins are target-derived factors necessary for mammalian nervous system development and maintenance. They are typically produced by neuronal target tissues and interact with their receptors at axonal endings. Therefore, locally generated neurotrophin signals must be conveyed from the axon back to the cell soma. Retrograde survival signaling by neurotrophin binding to Trk receptors has been extensively studied. However, neurotrophins also bind to the p75 receptor, which can induce apoptosis in a variety of contexts. Selective activation of p75 at distal axon ends has been shown to generate a retrograde apoptotic signal, although the mechanisms involved are poorly understood. The present review summarizes the available evidence for retrograde proapoptotic signaling in general and the role of the p75 receptor in particular, with discussion of unanswered questions in the field. In-depth knowledge of the mechanisms of retrograde apoptotic signaling is essential for understanding the etiology of neurodegeneration in many diseases and injuries.
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