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O-GlcNAc transferase inhibits visceral fat lipolysis and promotes diet-induced obesity.


ABSTRACT: Excessive visceral fat accumulation is a primary risk factor for metabolically unhealthy obesity and related diseases. The visceral fat is highly susceptible to the availability of external nutrients. Nutrient flux into the hexosamine biosynthetic pathway leads to protein posttranslational modification by O-linked β-N-acetylglucosamine (O-GlcNAc) moieties. O-GlcNAc transferase (OGT) is responsible for the addition of GlcNAc moieties to target proteins. Here, we report that inducible deletion of adipose OGT causes a rapid visceral fat loss by specifically promoting lipolysis in visceral fat. Mechanistically, visceral fat maintains a high level of O-GlcNAcylation during fasting. Loss of OGT decreases O-GlcNAcylation of lipid droplet-associated perilipin 1 (PLIN1), which leads to elevated PLIN1 phosphorylation and enhanced lipolysis. Moreover, adipose OGT overexpression inhibits lipolysis and promotes diet-induced obesity. These findings establish an essential role for OGT in adipose tissue homeostasis and indicate a unique potential for targeting O-GlcNAc signaling in the treatment of obesity.

SUBMITTER: Yang Y 

PROVIDER: S-EPMC6954210 | biostudies-literature | 2020 Jan

REPOSITORIES: biostudies-literature

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O-GlcNAc transferase inhibits visceral fat lipolysis and promotes diet-induced obesity.

Yang Yunfan Y   Fu Minnie M   Li Min-Dian MD   Zhang Kaisi K   Zhang Bichen B   Wang Simeng S   Liu Yuyang Y   Ni Weiming W   Ong Qunxiang Q   Mi Jia J   Yang Xiaoyong X  

Nature communications 20200110 1


Excessive visceral fat accumulation is a primary risk factor for metabolically unhealthy obesity and related diseases. The visceral fat is highly susceptible to the availability of external nutrients. Nutrient flux into the hexosamine biosynthetic pathway leads to protein posttranslational modification by O-linked β-N-acetylglucosamine (O-GlcNAc) moieties. O-GlcNAc transferase (OGT) is responsible for the addition of GlcNAc moieties to target proteins. Here, we report that inducible deletion of  ...[more]

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