Glial-derived mitochondrial signals affect neuronal proteostasis and aging

Author:

Bar-Ziv Raz1ORCID,Dutta Naibedya2,Hruby Adam2ORCID,Sukarto Edward1ORCID,Averbukh Maxim2ORCID,Alcala Athena2,Henderson Hope R.1ORCID,Durieux Jenni1ORCID,Tronnes Sarah U.1ORCID,Ahmad Qazi1ORCID,Bolas Theodore1,Perez Joel1ORCID,Dishart Julian G.1ORCID,Vega Matthew2,Garcia Gilberto2ORCID,Higuchi-Sanabria Ryo2ORCID,Dillin Andrew1ORCID

Affiliation:

1. Department of Molecular and Cellular Biology, Howard Hughes Medical Institute, The University of California, Berkeley, Berkeley, CA 94720, USA.

2. Leonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089, USA.

Abstract

The nervous system plays a critical role in maintaining whole-organism homeostasis; neurons experiencing mitochondrial stress can coordinate the induction of protective cellular pathways, such as the mitochondrial unfolded protein response (UPR MT ), between tissues. However, these studies largely ignored nonneuronal cells of the nervous system. Here, we found that UPR MT activation in four astrocyte-like glial cells in the nematode, Caenorhabditis elegans , can promote protein homeostasis by alleviating protein aggregation in neurons. Unexpectedly, we find that glial cells use small clear vesicles (SCVs) to signal to neurons, which then relay the signal to the periphery using dense-core vesicles (DCVs). This work underlines the importance of glia in establishing and regulating protein homeostasis within the nervous system, which can then affect neuron-mediated effects in organismal homeostasis and longevity.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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