The Troyer syndrome protein spartin mediates selective autophagy of lipid droplets Journal Article


Authors: Chung, J.; Park, J.; Lai, Z. W.; Lambert, T. J.; Richards, R. C.; Zhang, J. C.; Walther, T. C.; Farese, R. V., Jr.
Article Title: The Troyer syndrome protein spartin mediates selective autophagy of lipid droplets
Abstract: Lipid droplets (LDs) are crucial organelles for energy storage and lipid homeostasis. Autophagy of LDs is an important pathway for their catabolism, but the molecular mechanisms mediating LD degradation by selective autophagy (lipophagy) are unknown. Here we identify spartin as a receptor localizing to LDs and interacting with core autophagy machinery, and we show that spartin is required to deliver LDs to lysosomes for triglyceride mobilization. Mutations in SPART (encoding spartin) lead to Troyer syndrome, a form of complex hereditary spastic paraplegia(1). Interfering with spartin function in cultured human neurons or murine brain neurons leads to LD and triglyceride accumulation. Our identification of spartin as a lipophagy receptor, thus, suggests that impaired LD turnover contributes to Troyer syndrome development.
Keywords: ubiquitin; neurons; enzyme; identification; binding; motif; platform; lipophagy; spg20; ddhd2
Journal Title: Nature Cell Biology
ISSN: 1465-7392
Publisher: Nature Publishing Group  
Publication status: Online ahead of print
Date Published: 2023-01-01
Online Publication Date: 2023-01-01
Language: English
ACCESSION: WOS:001054192500002
DOI: 10.1038/s41556-023-01178-w
PROVIDER: wos
Notes: Article; Early Access -- Source: Wos
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