Literature DB >> 33600813

Maintenance of protein homeostasis in glia extends lifespan in C. elegans.

Lei Wang1, Laura Bianchi2.   

Abstract

Mounting evidence support that glia play a key role in organismal ageing. However, the mechanisms by which glia impact ageing are not understood. One of the processes that has significant impact on the rate of ageing is the unfolded protein response. The more robust the UPR, the more the organism can counteract the effect of environmental and genetic stressors. However, how decline of cellular UPR translates into organismal ageing and eventual death is not fully understood. Here we discuss recent findings highlighting that neuropeptides released by glia act long distance to regulate ageing in C. elegans. Taking advantage of the short lifespan and the genetic amenability of this organism, the endoplasmic reticulum unfolded protein responses (UPRER) can be activated in C. elegans glia. This leads to cell-nonautonomous activation of the UPRER in the intestine. Activation of intestinal UPRER requires the function of genes involved in neuropeptide processing and release, suggesting that neuropeptides signal from glia to the intestine to regulate ER stress response. Importantly, the cell-nonautonomous activation of UPRER leads to extension of lifespan. Taken together, these data suggest that environmental and genetic factors that impact the response of glia to stress have the potential to influence organismal ageing. Further research on the specific neuropeptides involved should cast new light on the mechanism of ageing and may suggest novel anti-ageing therapies.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ageing; C. elegans; Glia; Neuropeptides; Stress; Unfolded protein response

Mesh:

Substances:

Year:  2021        PMID: 33600813      PMCID: PMC8848293          DOI: 10.1016/j.expneurol.2021.113648

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  85 in total

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Review 2.  Endoplasmic reticulum and the unfolded protein response: dynamics and metabolic integration.

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Journal:  Science       Date:  2008-10-31       Impact factor: 47.728

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Authors:  Shanqing Zheng; Hilton Chiu; Jeffrey Boudreau; Tony Papanicolaou; William Bendena; Ian Chin-Sang
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Authors:  Matthew M Boisvert; Galina A Erikson; Maxim N Shokhirev; Nicola J Allen
Journal:  Cell Rep       Date:  2018-01-02       Impact factor: 9.423

8.  Regulated Ire1-dependent decay of messenger RNAs in mammalian cells.

Authors:  Julie Hollien; Jonathan H Lin; Han Li; Nicole Stevens; Peter Walter; Jonathan S Weissman
Journal:  J Cell Biol       Date:  2009-08-03       Impact factor: 10.539

9.  In vivo function of Hsp90 is dependent on ATP binding and ATP hydrolysis.

Authors:  W M Obermann; H Sondermann; A A Russo; N P Pavletich; F U Hartl
Journal:  J Cell Biol       Date:  1998-11-16       Impact factor: 10.539

10.  Role of the chaperonin cofactor Hsp10 in protein folding and sorting in yeast mitochondria.

Authors:  J Höhfeld; F U Hartl
Journal:  J Cell Biol       Date:  1994-07       Impact factor: 10.539

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