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Dietary fatty acids promote lipid droplet diversity through seipin enrichment in an ER subdomain.


ABSTRACT: Exogenous metabolites from microbial and dietary origins have profound effects on host metabolism. Here, we report that a sub-population of lipid droplets (LDs), which are conserved organelles for fat storage, is defined by metabolite-modulated targeting of the C. elegans seipin ortholog, SEIP-1. Loss of SEIP-1 function reduces the size of a subset of LDs while over-expression of SEIP-1 has the opposite effect. Ultrastructural analysis reveals SEIP-1 enrichment in an endoplasmic reticulum (ER) subdomain, which co-purifies with LDs. Analyses of C. elegans and bacterial genetic mutants indicate a requirement of polyunsaturated fatty acids (PUFAs) and microbial cyclopropane fatty acids (CFAs) for SEIP-1 enrichment, as confirmed by dietary supplementation experiments. In mammalian cells, heterologously expressed SEIP-1 engages nascent lipid droplets and promotes their subsequent expansion in a conserved manner. Our results suggest that microbial and polyunsaturated fatty acids serve unexpected roles in regulating cellular fat storage by promoting LD diversity.

SUBMITTER: Cao Z 

PROVIDER: S-EPMC6602954 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

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Dietary fatty acids promote lipid droplet diversity through seipin enrichment in an ER subdomain.

Cao Zhe Z   Hao Yan Y   Fung Chun Wing CW   Lee Yiu Yiu YY   Wang Pengfei P   Li Xuesong X   Xie Kang K   Lam Wen Jiun WJ   Qiu Yifei Y   Tang Ben Zhong BZ   Shui Guanghou G   Liu Pingsheng P   Qu Jianan J   Kang Byung-Ho BH   Mak Ho Yi HY  

Nature communications 20190701 1


Exogenous metabolites from microbial and dietary origins have profound effects on host metabolism. Here, we report that a sub-population of lipid droplets (LDs), which are conserved organelles for fat storage, is defined by metabolite-modulated targeting of the C. elegans seipin ortholog, SEIP-1. Loss of SEIP-1 function reduces the size of a subset of LDs while over-expression of SEIP-1 has the opposite effect. Ultrastructural analysis reveals SEIP-1 enrichment in an endoplasmic reticulum (ER) s  ...[more]

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