A neuropeptide regulates cell non-autonomous protein homeostasis
Year: 2026
Type: article
Abstract: The coordination of proteostasis between the brain and peripheral tissues is essential for the health and survival of all animals. In C . elegans , glia coordinate organismal proteostasis and longevity via the unfolded protein response of the endoplasmic reticulum (UPR ER ). However, the signaling molecules required remain unknown. Here, we show that glial UPR ER activation increases levels of specific neuropeptides. We identify a single neuropeptide, FLP-17, that is sufficient but not necessary to induce cell non-autonomous activation of the UPR ER and protect against chronic ER stress. FLP-17 signals partially through the receptor, EGL-6, to activate transcellular UPR ER and confer stress resistance. Both XBP-1 and PERK are required for maximal FLP-17-induced UPR ER activation, though only XBP-1 is necessary for organismal ER stress resistance. This work reveals a complex neuropeptide network initiated by glial UPR ER activation and identifies FLP-17 as a critical mediator that coopts an existing sensory-metabolic circuit to coordinate organismal proteostasis.
Source: Cell Reports
Language: English
Subfield: Cell Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $5,620
Funders: U.S. Department of Health and Human Services, Glenn Foundation for Medical Research, National Institutes of Health, National Institute on Aging, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases
OpenAlex ID: W7143405243
