Glial-derived mitochondrial signals impact neuronal proteostasis and aging. 2023

Raz Bar-Ziv, and Naibedya Dutta, and Adam Hruby, and Edward Sukarto, and Maxim Averbukh, and Athena Alcala, and Hope R Henderson, and Jenni Durieux, and Sarah U Tronnes, and Qazi Ahmad, and Theodore Bolas, and Joel Perez, and Julian G Dishart, and Matthew Vega, and Gilberto Garcia, and Ryo Higuchi-Sanabria, and Andrew Dillin
Department of Molecular & Cellular Biology, Howard Hughes Medical Institute, The University of California, Berkeley, Berkeley CA 94720, USA.

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 (UPRMT), between tissues. However, these studies largely ignored non-neuronal cells of the nervous system. Here, we found that UPRMT activation in four, astrocyte-like glial cells in the nematode, C. elegans, can promote protein homeostasis by alleviating protein aggregation in neurons. Surprisingly, we find that glial cells utilize 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 impact neuron-mediated effects in organismal homeostasis and longevity.

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