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Mig-6 is essential for glucose homeostasis and thermogenesis in brown adipose tissue.
Choung, Sorim; Kim, Ji Min; Joung, Kyong Hye; Kim, Hyun Jin; Kang, Seon Mee; Jeong, Jae-Wook; Ku, Bon Jeong.
Affiliation
  • Choung S; Research Institute for Medical Science, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea. Electronic address: thfla79@naver.com.
  • Kim JM; Department of Endocrinology, Chungnam National University Sejong Hospital, Sejong, 30099, Republic of Korea; Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea.
  • Joung KH; Department of Endocrinology, Chungnam National University Sejong Hospital, Sejong, 30099, Republic of Korea; Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea.
  • Kim HJ; Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea.
  • Kang SM; Department of Internal Medicine, Busan Paik Hospital, College of Medicine, Inje University, Busan, 47392, Republic of Korea.
  • Jeong JW; Department of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, Grand Rapids, MI, 49503, USA.
  • Ku BJ; Research Institute for Medical Science, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea; Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea. Electronic address: bonjeong@cnu.ac.kr.
Biochem Biophys Res Commun ; 572: 92-97, 2021 10 01.
Article in En | MEDLINE | ID: mdl-34358969
ABSTRACT
Brown adipose tissue (BAT) is an anti-obese and anti-diabetic tissue that stimulates energy expenditure in the form of adaptive thermogenesis through uncoupling protein 1 (UCP1). Mitogen-inducible gene-6 (Mig-6) is a negative regulator of epidermal growth factor receptor (EGFR) that interacts with many cellular partners and has multiple cellular functions. We have recently reported that Mig-6 is associated with diabetes and metabolic syndrome. However, its function in BAT is unknown. We generated a brown adipocyte-specific Mig-6 knock-in mouse (BKI) to examine the role of Mig-6 in BAT. Mig-6 BKI mice had improved glucose tolerance on a normal chow diet. Mig-6 BKI mice also revealed activated thermogenesis and the size of the BAT lipid droplets was reduced. Additionally, Mig-6 regulated cAMP-PKA signaling-induced UCP1 expression in brown adipocytes. Taken together, these results demonstrate that Mig-6 affects glucose tolerance and thermogenesis in BAT.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adipose Tissue, Brown / Intracellular Signaling Peptides and Proteins / Glucose Limits: Animals Language: En Journal: Biochem Biophys Res Commun Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adipose Tissue, Brown / Intracellular Signaling Peptides and Proteins / Glucose Limits: Animals Language: En Journal: Biochem Biophys Res Commun Year: 2021 Document type: Article
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