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Download fileMutations of NRG4 Contribute to the Pathogenesis of Non-Alcoholic Fatty Liver Disease and Related Metabolic Disorders
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posted on 2021-07-14, 17:59 authored by Yangyang Li, Li Jin, Feng Jiang, Jing Yan, Yan Lu, Qing Yang, Yi Zhang, Hong Zhang, Hairong Yu, Yuemei Zhang, Zhen He, Rong Zhang, Jianjun Yang, Cheng HuNeuregulin 4 (Nrg4), an adipose tissue–enriched endocrine factor,
participates in adipocyte-to-hepatocyte communication, eliciting beneficial
metabolic effects in non-alcoholic fatty
liver disease (NAFLD). Here, we evaluate the physiological roles of Nrg4 in humans and unravel
the role of NRG4 variants in the pathogenesis of NAFLD and related
metabolic disorders. We identified two rare missense mutations—p. R44H and p.E47Q— in the NRG4 EGFL
domain by whole exome sequencing in 224 severely obese subjects and exome genotyping
in 2,388 subjects from Shanghai Obesity Study. The over-expression animal models showed
wild-type (WT) Nrg4 could attenuate high-fat diet-induced hepatic lipogenesis
and improve energy metabolism. Nrg4 E47Q enhanced the protective effect, whereas
Nrg4 R44H lost this function. Unlike Nrg4 R44H, Nrg4 E47Q activated the phosphorylation
of ErbB4 and negatively regulated the de novo lipogenesis via the
ErbB4-STAT5-SREBP1C pathway. The surface plasmon resonance experiments revealed
a higher affinity of E47Q Nrg4 than WT to bind ErbB4, while R44H showed no binding. In conclusion, the study suggests
that genetic variations in NRG4 could produce mutant proteins with
aberrant functions, and impaired or enhanced Nrg4 function could either be a
risk factor or protective factor for NAFLD and associated metabolic disorders.