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Retrograde apoptotic signaling by the p75 neurotrophin receptor

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 ba...

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Detalles Bibliográficos
Autores principales: Pathak, Amrita, Carter, Bruce D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373242/
https://www.ncbi.nlm.nih.gov/pubmed/32714573
http://dx.doi.org/10.1042/NS20160007
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author Pathak, Amrita
Carter, Bruce D.
author_facet Pathak, Amrita
Carter, Bruce D.
author_sort Pathak, Amrita
collection PubMed
description 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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spelling pubmed-73732422020-07-23 Retrograde apoptotic signaling by the p75 neurotrophin receptor Pathak, Amrita Carter, Bruce D. Neuronal Signal Review Articles 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. Portland Press Ltd. 2017-02-24 /pmc/articles/PMC7373242/ /pubmed/32714573 http://dx.doi.org/10.1042/NS20160007 Text en © 2017 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).
spellingShingle Review Articles
Pathak, Amrita
Carter, Bruce D.
Retrograde apoptotic signaling by the p75 neurotrophin receptor
title Retrograde apoptotic signaling by the p75 neurotrophin receptor
title_full Retrograde apoptotic signaling by the p75 neurotrophin receptor
title_fullStr Retrograde apoptotic signaling by the p75 neurotrophin receptor
title_full_unstemmed Retrograde apoptotic signaling by the p75 neurotrophin receptor
title_short Retrograde apoptotic signaling by the p75 neurotrophin receptor
title_sort retrograde apoptotic signaling by the p75 neurotrophin receptor
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7373242/
https://www.ncbi.nlm.nih.gov/pubmed/32714573
http://dx.doi.org/10.1042/NS20160007
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