脂肪生成
脂肪细胞
MAPK/ERK通路
内分泌学
脂质代谢
内科学
肥胖
肽
生物
体内
化学
医学
脂肪组织
信号转导
细胞生物学
生物化学
生物技术
作者
Yun Li,Xianwei Cui,Xing Wang,Dan Shen,Anwen Yin,Lianghui You,Juan Wen,Chenbo Ji,Xirong Guo
标识
DOI:10.1016/j.bbagen.2020.129836
摘要
Emerging evidence revealed peptides within breast milk may be an abundant source of potential candidates for metabolism regulation. Our previous work identified numerous peptides existed in breast milk, but its function has not been validated. Thus, our study aims to screen for novel peptides that have the potential to antagonize obesity and diabetes.A function screen was designed to identify the candidate peptide and then the peptide effect was validated by assessing lipid storage. Afterwards, the in vivo study was performed in two obese models: high-fat diet (HFD)-induced obese mice and obese ob/ob mice. For mechanism study, a RNA-seq analysis was conducted to explore the pathway that account for the biological function of peptide.By performing a small scale screening, a peptide (AVPVQALLLNQ) termed AOPDM1 (anti-obesity peptide derived from breast milk 1) was identified to reduce lipid storage in adipocytes. Further study showed AOPDM1 suppressed adipocyte differentiation by sustaining ERK activity at later stage of differentiation which down-regulated PPARγ expression. In vivo, AOPDM1 effectively reduced fat mass and improved glucose metabolism in high-fat diet (HFD)-induced obese mice and obese ob/ob mice.We identified a novel peptide AOPDM1 derived from breast milk could restrict adipocyte differentiation and ameliorate obesity through regulating MAPK pathway.Our findings may provide a potential candidate for the discovery of therapeutic drugs for obesity and type 2 diabetes.
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