Dysfunctional autophagy is a driver of muscle stem cell functional decline with aging

54Citations
Citations of this article
81Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

abstract: Regeneration of skeletal muscle relies on its resident stem cells, also known as satellite cells, which are normally quiescent. With aging, satellite cell quiescence is lost concomitant with a muscle regenerative decline. Here we demonstrate that autophagy sustains quiescence over time and that its failure with age drives senescence, which accounts for stem cell loss of function. Pharmacological and genetic reestablishment of autophagy restores homeostasis and regenerative functions in geriatric satellite cells, which has relevance for the elderly population.

Cited by Powered by Scopus

The quest to slow ageing through drug discovery

310Citations
N/AReaders
Get full text

NAD<sup>+</sup> metabolism, stemness, the immune response, and cancer

291Citations
N/AReaders
Get full text

Mitophagy in human diseases

161Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

García-Prat, L., Muñoz-Cánoves, P., & Martinez-Vicente, M. (2016). Dysfunctional autophagy is a driver of muscle stem cell functional decline with aging. Autophagy. Taylor and Francis Inc. https://doi.org/10.1080/15548627.2016.1143211

Readers over time

‘16‘17‘18‘19‘20‘21‘22‘23‘24‘2505101520

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 29

63%

Researcher 13

28%

Professor / Associate Prof. 2

4%

Lecturer / Post doc 2

4%

Readers' Discipline

Tooltip

Biochemistry, Genetics and Molecular Bi... 28

56%

Agricultural and Biological Sciences 15

30%

Sports and Recreations 5

10%

Medicine and Dentistry 2

4%

Save time finding and organizing research with Mendeley

Sign up for free
0