Omics approach to reveal the effects of obesity on the protein profiles of the exosomes derived from different adipose depots

脂肪组织 组学 微泡 计算生物学 肥胖 生物信息学 生物 外体 内分泌学 数据科学 生物化学 小RNA 计算机科学 医学 基因
作者
Minting Chen,Fan Zhang,Baisen Chen,Condon Lau,Chuying Huo,Quan‐Bin Han,Tao Su,Hiu Yee Kwan
出处
期刊:Research Square - Research Square
标识
DOI:10.21203/rs.3.rs-1544257/v1
摘要

Abstract Background: Obesity affects the cargo packaging of the adipocyte-derived exosomes. Furthermore, adipocytes in different adipose tissues have different genetic makeup, the cargo contents of the exosomes derived from different adipose tissues under obesity should be different, and hence their impacts on the pathophysiological conditions. Methods and Results: iTRAQ-based quantitative proteomics show that obesity has more prominent effects on the protein profiles of the exosomes derived from subcutaneous adipose tissue (SAT-Exos) in the diet-induced obesity (DIO) mice than those derived from epididymal adipose tissue (EAT-Exos) and visceral adipose tissue (VAT-Exos). The differential expressed proteins (DEPs) in SAT-Exos and VAT-Exos are mainly involved in metabolism. Subsequent untargeted metabolomic and lipidomics analysis reveal that injection of these SAT-Exos into the B6/J-Rab27a-Cas9-KO mice significantly affects the mouse metabolism such as fatty acid metabolism. Some of the DEPs in SAT-Exos are correlated with fatty acid metabolism including ADP-ribosylation factor and mitogen-activated protein kinase kinase kinase-3. Pathway analysis also shows that SAT-Exos affect adipocyte lipolysis and glycerophospholipid metabolism, which is in parallel with the enhanced plasma levels of fatty acids, diglycerides, monoglycerides and the changes in glycerophospholipid levels in DIO mice. Conclusion: Our data provide evidence to suggest SAT-Exos contribute to the changes in plasma lipid profiles under obesity conditions.
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