期刊
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
卷 117, 期 52, 页码 33282-33294出版社
NATL ACAD SCIENCES
DOI: 10.1073/pnas.2011124117
关键词
fatty acid (FA); desaturase; sorting nexin 14; SCAR20 disease; lipid droplet (LD)
资金
- Welch Foundation [I-1873]
- Searle Foundation [SSP-2016-1482]
- NIH National Institute of General Medical Sciences [GM119768]
- University of Texas Southwestern Endowed Scholars Program
- American Heart Association Predoctoral Fellowship Grant [20PRE35210230]
- NIH [2 PO1 HL20948-33]
Fatty acids (FAs) are central cellular metabolites that contribute to lipid synthesis, and can be stored or harvested for metabolic energy. Dysregulation in FA processing and storage causes toxic FA accumulation or altered membrane compositions and contributes to metabolic and neurological disorders. Saturated lipids are particularly detrimental to cells, but how lipid saturation levels are maintained remains poorly understood. Here, we identify the cerebellar ataxia spinocerebellar ataxia, autosomal recessive 20 (SCAR20)-associated protein Snx14, an endoplasmic reticulum (ER)-lipid droplet (LD) tethering protein, as a factor required to maintain the lipid saturation balance of cell membranes. We show that following saturated FA (SFA) treatment, the ER integrity of SNX14(KO) cells is compromised, and both SNX14(KO) cells and SCAR20 disease patient-derived cells are hypersensitive to SFA-mediated lipotoxic cell death. Using APEX2-based proximity labeling, we reveal the protein composition of Snx14-associated ER-LD contacts and define a functional interaction between Snx14 and Delta-9 FA desaturase SCD1. Lipidomic profiling reveals that SNX14(KO) cells increase membrane lipid saturation following exposure to palmitate, phenocopying cells with perturbed SCD1 activity. In line with this, SNX14(KO) cells manifest delayed FA processing and lipotoxicity, which can be rescued by SCD1 overexpression. Altogether, these mechanistic insights reveal a role for Snx14 in FA and ER homeostasis, defects in which may underlie the neuropathology of SCAR20.
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