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本文引用的文献

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Adipocyte-secreted exosomal microRNA-34a inhibits M2 macrophage polarization to promote obesity-induced adipose inflammation.脂肪细胞分泌的细胞外体 microRNA-34a 抑制 M2 巨噬细胞极化,促进肥胖诱导的脂肪组织炎症。
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A dual Ucp1 reporter mouse model for imaging and quantitation of brown and brite fat recruitment.一种用于成像和定量棕色和米色脂肪募集的双重 Ucp1 报告小鼠模型。
Mol Metab. 2019 Feb;20:14-27. doi: 10.1016/j.molmet.2018.11.009. Epub 2018 Nov 28.
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Estrogen-mediated gut microbiome alterations influence sexual dimorphism in metabolic syndrome in mice.雌激素介导的肠道微生物组改变影响小鼠代谢综合征的性别二态性。
Microbiome. 2018 Nov 13;6(1):205. doi: 10.1186/s40168-018-0587-0.
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Activation of estrogen receptor alpha induces beiging of adipocytes.雌激素受体α的激活诱导脂肪细胞的米色化。
Mol Metab. 2018 Dec;18:51-59. doi: 10.1016/j.molmet.2018.09.002. Epub 2018 Sep 15.
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Sex-Dimorphic and Sex Hormone-Dependent Role of Steroid Sulfatase in Adipose Inflammation and Energy Homeostasis.甾体硫酸酯酶在脂肪炎症和能量稳态中的性别二态和性激素依赖性作用。
Endocrinology. 2018 Sep 1;159(9):3365-3377. doi: 10.1210/en.2018-00531.
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Glucocorticoids, Sex Hormones, and Immunity.糖皮质激素、性激素与免疫
Front Immunol. 2018 Jun 12;9:1332. doi: 10.3389/fimmu.2018.01332. eCollection 2018.
7
Sexual dimorphism in bacterial infections.细菌感染中的性别二态性。
Biol Sex Differ. 2018 Jun 20;9(1):27. doi: 10.1186/s13293-018-0187-5.
8
Ovarian Hormones Regulate the Production of Adipocytes From Bone Marrow-Derived Cells.卵巢激素调节骨髓来源细胞中脂肪细胞的生成。
Front Endocrinol (Lausanne). 2018 May 28;9:276. doi: 10.3389/fendo.2018.00276. eCollection 2018.
9
Central regulation of energy metabolism by estrogens.雌激素对能量代谢的中枢调节。
Mol Metab. 2018 Sep;15:104-115. doi: 10.1016/j.molmet.2018.05.012. Epub 2018 May 23.
10
Connecting the immune system, systemic chronic inflammation and the gut microbiome: The role of sex.连接免疫系统、系统性慢性炎症和肠道微生物组:性别的作用。
J Autoimmun. 2018 Aug;92:12-34. doi: 10.1016/j.jaut.2018.05.008. Epub 2018 Jun 1.

雌激素、脂肪组织与女性生殖代谢之间的免疫代谢联系

Immunometabolic Links between Estrogen, Adipose Tissue and Female Reproductive Metabolism.

作者信息

Eaton Sally A, Sethi Jaswinder K

机构信息

Human Development and Health, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.

National Institute for Health Research Biomedical Research Centre Southampton, University Hospital Southampton NHS foundation Trust, Southampton General Hospital, Southampton SO16 6YD, UK.

出版信息

Biology (Basel). 2019 Feb 7;8(1):8. doi: 10.3390/biology8010008.

DOI:10.3390/biology8010008
PMID:30736459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6466614/
Abstract

The current knowledge of sex-dependent differences in adipose tissue biology remains in its infancy and is motivated in part by the desire to understand why menopause is linked to an increased risk of metabolic disease. However, the development and characterization of targeted genetically-modified rodent models are shedding new light on the physiological actions of sex hormones in healthy reproductive metabolism. In this review we consider the need for differentially regulating metabolic flexibility, energy balance, and immunity in a sex-dependent manner. We discuss the recent advances in our understanding of physiological roles of systemic estrogen in regulating sex-dependent adipose tissue distribution, form and function; and in sex-dependent healthy immune function. We also review the decline in protective properties of estrogen signaling in pathophysiological settings such as obesity-related metaflammation and metabolic disease. It is clear that the many physiological actions of estrogen on energy balance, immunity, and immunometabolism together with its dynamic regulation in females make it an excellent candidate for regulating metabolic flexibility in the context of reproductive metabolism.

摘要

目前对于脂肪组织生物学中性别差异的认识仍处于起步阶段,部分原因是人们渴望了解为何更年期与代谢疾病风险增加相关。然而,靶向基因修饰啮齿动物模型的开发和特性研究正在为性激素在健康生殖代谢中的生理作用带来新的见解。在这篇综述中,我们探讨了以性别依赖方式差异调节代谢灵活性、能量平衡和免疫的必要性。我们讨论了近期在理解全身雌激素在调节性别依赖的脂肪组织分布、形态和功能以及性别依赖的健康免疫功能方面生理作用的进展。我们还回顾了在肥胖相关的元炎症和代谢疾病等病理生理环境中雌激素信号保护特性的下降。很明显,雌激素在能量平衡、免疫和免疫代谢方面的多种生理作用及其在女性中的动态调节使其成为在生殖代谢背景下调节代谢灵活性的极佳候选者。