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产热脂肪组织在能量消耗中的作用。

The Role of Thermogenic Fat Tissue in Energy Consumption.

作者信息

Horino Masato, Ikeda Kenji, Yamada Tetsuya

机构信息

Department of Molecular Endocrinology and Metabolism, Tokyo Medical and Dental University, Tokyo 113-8519, Japan.

出版信息

Curr Issues Mol Biol. 2022 Jul 11;44(7):3166-3179. doi: 10.3390/cimb44070219.

DOI:10.3390/cimb44070219
PMID:35877443
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9317885/
Abstract

Mammalian adipose tissues are broadly divided into white adipose tissue (WAT) and thermogenic fat tissue (brown adipose tissue and beige adipose tissue). Uncoupling protein 1 (UCP1) is the central protein in thermogenesis, and cells that exhibit induced UCP1 expression and appear scattered throughout WAT are called beige adipocytes, and their induction in WAT is referred to as "beiging". Beige adipocytes can differentiate from preadipocytes or convert from mature adipocytes. UCP1 was thought to contribute to non-shivering thermogenesis; however, recent studies demonstrated the presence of UCP1-independent thermogenic mechanisms. There is evidence that thermogenic fat tissue contributes to systemic energy expenditure even in human beings. This review discusses the roles that thermogenic fat tissue plays in energy consumption and offers insight into the possibility and challenges associated with its application in the treatment of obesity and type 2 diabetes.

摘要

哺乳动物的脂肪组织大致可分为白色脂肪组织(WAT)和产热脂肪组织(棕色脂肪组织和米色脂肪组织)。解偶联蛋白1(UCP1)是产热过程中的核心蛋白,在白色脂肪组织中呈现诱导型UCP1表达且散在分布的细胞被称为米色脂肪细胞,其在白色脂肪组织中的诱导过程被称为“米色化”。米色脂肪细胞可由前脂肪细胞分化而来,也可由成熟脂肪细胞转变而来。UCP1曾被认为有助于非颤抖性产热;然而,最近的研究表明存在不依赖UCP1的产热机制。有证据表明,即使在人类中,产热脂肪组织也有助于全身能量消耗。本综述讨论了产热脂肪组织在能量消耗中所起的作用,并深入探讨了其在肥胖症和2型糖尿病治疗应用中的可能性及挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9317885/30d0dde784af/cimb-44-00219-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9317885/58815b8275b8/cimb-44-00219-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9317885/f1a72f9b401b/cimb-44-00219-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9317885/30d0dde784af/cimb-44-00219-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9317885/58815b8275b8/cimb-44-00219-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9317885/f1a72f9b401b/cimb-44-00219-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9317885/30d0dde784af/cimb-44-00219-g003.jpg

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本文引用的文献

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Liraglutide suppresses obesity and promotes browning of white fat via miR-27b and .利拉鲁肽通过 miR-27b 和 抑制肥胖并促进白色脂肪的棕色化。
J Int Med Res. 2021 Nov;49(11):3000605211055059. doi: 10.1177/03000605211055059.
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The chemerin-CMKLR1 axis limits thermogenesis by controlling a beige adipocyte/IL-33/type 2 innate immunity circuit.Chemerin-CMKLR1 轴通过控制米色脂肪细胞/IL-33/2 型先天免疫回路来限制产热。
Sci Immunol. 2021 Jul 30;6(61). doi: 10.1126/sciimmunol.abg9698.
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Potential Functions of the BMP Family in Bone, Obesity, and Glucose Metabolism.
骨、肥胖和葡萄糖代谢中 BMP 家族的潜在功能。
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FGF21 promotes thermogenic gene expression as an autocrine factor in adipocytes.成纤维细胞生长因子 21(FGF21)作为脂肪细胞的自分泌因子促进产热基因表达。
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Peripheral IL-6/STAT3 signaling promotes beiging of white fat.外周白细胞介素 6/STAT3 信号促进白色脂肪的米色化。
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The cellular and functional complexity of thermogenic fat.产热脂肪的细胞和功能复杂性。
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PPARgamma in Metabolism, Immunity, and Cancer: Unified and Diverse Mechanisms of Action.PPARγ 在代谢、免疫和癌症中的作用:统一和多样化的作用机制。
Front Endocrinol (Lausanne). 2021 Feb 26;12:624112. doi: 10.3389/fendo.2021.624112. eCollection 2021.
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Creatine kinase B controls futile creatine cycling in thermogenic fat.肌酸激酶B控制产热脂肪中的无效肌酸循环。
Nature. 2021 Feb;590(7846):480-485. doi: 10.1038/s41586-021-03221-y. Epub 2021 Feb 17.
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