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Mitochondria-derived peptide SHLP2 regulates energy homeostasis through the activation of hypothalamic neurons.open access

Authors
Kim, Seul KiTran, Le TrungNamKoong, CherlChoi, Hyung JinChun, Hye JinLee, Yong-HoCheon, MyungHyunChung, ChiHyeHwang, JunmoLim, Hyun-HoShin, Dong MinChoi, Yun-HeeKim, Ki Woo
Issue Date
Aug-2023
Publisher
Nature Publishing Group
Citation
Nature Communications, v.14, no.1, pp 4321
Journal Title
Nature Communications
Volume
14
Number
1
Start Page
4321
URI
http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/112
DOI
10.1038/s41467-023-40082-7
ISSN
2041-1723
2041-1723
Abstract
Small humanin-like peptide 2 (SHLP2) is a mitochondrial-derived peptide implicated in several biological processes such as aging and oxidative stress. However, its functional role in the regulation of energy homeostasis remains unclear, and its corresponding receptor is not identified. Hereby, we demonstrate that both systemic and intracerebroventricular (ICV) administrations of SHLP2 protected the male mice from high-fat diet (HFD)-induced obesity and improved insulin sensitivity. In addition, the activation of pro-opiomelanocortin (POMC) neurons by SHLP2 in the arcuate nucleus of the hypothalamus (ARC) is involved in the suppression of food intake and the promotion of thermogenesis. Through high-throughput structural complementation screening, we discovered that SHLP2 binds to and activates chemokine receptor 7 (CXCR7). Taken together, our study not only reveals the therapeutic potential of SHLP2 in metabolic disorders but also provides important mechanistic insights into how it exerts its effects on energy homeostasis. © 2023. The Author(s).
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연구본부 (신경·혈관단위체 연구그룹)
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