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Therapeutic targeting of autophagy in neurodegenerative and infectious diseases

Autophagy is a conserved process that uses double-membrane vesicles to deliver cytoplasmic contents to lysosomes for degradation. Although autophagy may impact many facets of human biology and disease, in this review we focus on the ability of autophagy to protect against certain neurodegenerative a...

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Autores principales: Rubinsztein, David C., Bento, Carla F., Deretic, Vojo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493419/
https://www.ncbi.nlm.nih.gov/pubmed/26101267
http://dx.doi.org/10.1084/jem.20150956
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author Rubinsztein, David C.
Bento, Carla F.
Deretic, Vojo
author_facet Rubinsztein, David C.
Bento, Carla F.
Deretic, Vojo
author_sort Rubinsztein, David C.
collection PubMed
description Autophagy is a conserved process that uses double-membrane vesicles to deliver cytoplasmic contents to lysosomes for degradation. Although autophagy may impact many facets of human biology and disease, in this review we focus on the ability of autophagy to protect against certain neurodegenerative and infectious diseases. Autophagy enhances the clearance of toxic, cytoplasmic, aggregate-prone proteins and infectious agents. The beneficial roles of autophagy can now be extended to supporting cell survival and regulating inflammation. Autophagic control of inflammation is one area where autophagy may have similar benefits for both infectious and neurodegenerative diseases beyond direct removal of the pathogenic agents. Preclinical data supporting the potential therapeutic utility of autophagy modulation in such conditions is accumulating.
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spelling pubmed-44934192015-12-29 Therapeutic targeting of autophagy in neurodegenerative and infectious diseases Rubinsztein, David C. Bento, Carla F. Deretic, Vojo J Exp Med Review Autophagy is a conserved process that uses double-membrane vesicles to deliver cytoplasmic contents to lysosomes for degradation. Although autophagy may impact many facets of human biology and disease, in this review we focus on the ability of autophagy to protect against certain neurodegenerative and infectious diseases. Autophagy enhances the clearance of toxic, cytoplasmic, aggregate-prone proteins and infectious agents. The beneficial roles of autophagy can now be extended to supporting cell survival and regulating inflammation. Autophagic control of inflammation is one area where autophagy may have similar benefits for both infectious and neurodegenerative diseases beyond direct removal of the pathogenic agents. Preclinical data supporting the potential therapeutic utility of autophagy modulation in such conditions is accumulating. The Rockefeller University Press 2015-06-29 /pmc/articles/PMC4493419/ /pubmed/26101267 http://dx.doi.org/10.1084/jem.20150956 Text en © 2015 Rubinsztein et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Review
Rubinsztein, David C.
Bento, Carla F.
Deretic, Vojo
Therapeutic targeting of autophagy in neurodegenerative and infectious diseases
title Therapeutic targeting of autophagy in neurodegenerative and infectious diseases
title_full Therapeutic targeting of autophagy in neurodegenerative and infectious diseases
title_fullStr Therapeutic targeting of autophagy in neurodegenerative and infectious diseases
title_full_unstemmed Therapeutic targeting of autophagy in neurodegenerative and infectious diseases
title_short Therapeutic targeting of autophagy in neurodegenerative and infectious diseases
title_sort therapeutic targeting of autophagy in neurodegenerative and infectious diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493419/
https://www.ncbi.nlm.nih.gov/pubmed/26101267
http://dx.doi.org/10.1084/jem.20150956
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