Suppr超能文献

磷酸胆碱积累和 PHOSPHO1 耗竭促进脂肪组织产热。

Phosphocholine accumulation and PHOSPHO1 depletion promote adipose tissue thermogenesis.

机构信息

Whitehead Institute for Biomedical Research, Cambridge, MA 02142.

Whitehead Institute for Biomedical Research, Cambridge, MA 02142;

出版信息

Proc Natl Acad Sci U S A. 2020 Jun 30;117(26):15055-15065. doi: 10.1073/pnas.1916550117. Epub 2020 Jun 17.

Abstract

Phosphocholine phosphatase-1 (PHOSPHO1) is a phosphocholine phosphatase that catalyzes the hydrolysis of phosphocholine (PC) to choline. Here we demonstrate that the PHOSPHO1 transcript is highly enriched in mature brown adipose tissue (BAT) and is further induced by cold and isoproterenol treatments of BAT and primary brown adipocytes. In defining the functional relevance of PHOPSPHO1 in BAT thermogenesis and energy metabolism, we show that PHOSPHO1 knockout mice are cold-tolerant, with higher expression of thermogenic genes in BAT, and are protected from high-fat diet-induced obesity and development of insulin resistance. Treatment of mice with the PHOSPHO1 substrate phosphocholine is sufficient to induce cold tolerance, thermogenic gene expression, and allied metabolic benefits. Our results reveal a role of PHOSPHO1 as a negative regulator of BAT thermogenesis, and inhibition of PHOSPHO1 or enhancement of phosphocholine represent innovative approaches to manage the metabolic syndrome.

摘要

磷酸胆碱磷酸酶 1(PHOSPHO1)是一种磷酸胆碱磷酸酶,可催化磷酸胆碱(PC)水解为胆碱。在这里,我们证明 PHOSPHO1 转录本在成熟棕色脂肪组织(BAT)中高度富集,并进一步受到冷和异丙肾上腺素处理 BAT 和原代棕色脂肪细胞的诱导。为了确定 PHOSPHO1 在 BAT 产热和能量代谢中的功能相关性,我们发现 PHOSPHO1 敲除小鼠对寒冷耐受,BAT 中产热基因表达更高,并且免受高脂肪饮食诱导的肥胖和胰岛素抵抗的发展。用 PHOSPHO1 的底物磷酸胆碱处理小鼠足以诱导耐寒性、产热基因表达和相关代谢益处。我们的结果揭示了 PHOSPHO1 作为 BAT 产热的负调节剂的作用,抑制 PHOSPHO1 或增强磷酸胆碱代表了管理代谢综合征的创新方法。

相似文献

1
Phosphocholine accumulation and PHOSPHO1 depletion promote adipose tissue thermogenesis.
Proc Natl Acad Sci U S A. 2020 Jun 30;117(26):15055-15065. doi: 10.1073/pnas.1916550117. Epub 2020 Jun 17.
2
p38α blocks brown adipose tissue thermogenesis through p38δ inhibition.
PLoS Biol. 2018 Jul 6;16(7):e2004455. doi: 10.1371/journal.pbio.2004455. eCollection 2018 Jul.
3
PACAP is essential for the adaptive thermogenic response of brown adipose tissue to cold exposure.
J Endocrinol. 2014 Sep;222(3):327-39. doi: 10.1530/JOE-14-0316. Epub 2014 Jul 23.
4
Cold-induction of afadin in brown fat supports its thermogenic capacity.
Sci Rep. 2021 May 7;11(1):9794. doi: 10.1038/s41598-021-89207-2.
5
MiR-22 modulates brown adipocyte thermogenesis by synergistically activating the glycolytic and mTORC1 signaling pathways.
Theranostics. 2021 Jan 25;11(8):3607-3623. doi: 10.7150/thno.50900. eCollection 2021.
6
The glycoprotein follistatin-like 1 promotes brown adipose thermogenesis.
Metabolism. 2019 Sep;98:16-26. doi: 10.1016/j.metabol.2019.05.008. Epub 2019 May 24.
7
PHOSPHO1 is a skeletal regulator of insulin resistance and obesity.
BMC Biol. 2020 Oct 22;18(1):149. doi: 10.1186/s12915-020-00880-7.
8
Enhanced phosphocholine metabolism is essential for terminal erythropoiesis.
Blood. 2018 Jun 28;131(26):2955-2966. doi: 10.1182/blood-2018-03-838516. Epub 2018 Apr 30.
9
JAK2 promotes brown adipose tissue function and is required for diet- and cold-induced thermogenesis in mice.
Diabetologia. 2016 Jan;59(1):187-196. doi: 10.1007/s00125-015-3786-2. Epub 2015 Oct 29.
10
Proteome Imbalance of Mitochondrial Electron Transport Chain in Brown Adipocytes Leads to Metabolic Benefits.
Cell Metab. 2018 Mar 6;27(3):616-629.e4. doi: 10.1016/j.cmet.2018.01.018.

引用本文的文献

1
Adipocyte CLDN5 promotes thermogenesis and energy expenditure through regulation of IL10 expression.
Nat Commun. 2025 Jul 4;16(1):6151. doi: 10.1038/s41467-025-61371-3.
2
Distinct bone metabolic networks identified in 1 mice vs. wild type mice using [F]FDG total-body PET.
Front Med (Lausanne). 2025 May 21;12:1597844. doi: 10.3389/fmed.2025.1597844. eCollection 2025.
4
Myristoylated Eepd1 Enhances Lipolysis and Thermogenesis through PKA Activation to Combat Obesity.
Nat Commun. 2025 Jan 14;16(1):651. doi: 10.1038/s41467-025-56026-2.
5
CD8 + T-Cell-Related Genes: Deciphering Their Role in the Pancreatic Adenocarcinoma TME and Their Effect on Prognosis.
Dig Dis Sci. 2025 Jan;70(1):262-284. doi: 10.1007/s10620-024-08715-z. Epub 2024 Nov 27.
6
Is choline kinase alpha a drug target for obesity?
Front Endocrinol (Lausanne). 2024 Nov 6;15:1492753. doi: 10.3389/fendo.2024.1492753. eCollection 2024.
7
Bone mineralisation and glucose metabolism.
Curr Opin Endocr Metab Res. 2023 Apr;29:100446. doi: 10.1016/j.coemr.2023.100446.
8
Repurposing lansoprazole to alleviate metabolic syndrome PHOSPHO1 inhibition.
Acta Pharm Sin B. 2024 Apr;14(4):1711-1725. doi: 10.1016/j.apsb.2024.01.001. Epub 2024 Jan 4.
9
Phosphocholine-induced energy source shift alleviates mitochondrial dysfunction in lung cells caused by geospecific PM components.
Proc Natl Acad Sci U S A. 2024 Apr 2;121(14):e2317574121. doi: 10.1073/pnas.2317574121. Epub 2024 Mar 26.

本文引用的文献

1
Blood-Based DNA Methylation Biomarkers for Type 2 Diabetes: Potential for Clinical Applications.
Front Endocrinol (Lausanne). 2018 Dec 4;9:744. doi: 10.3389/fendo.2018.00744. eCollection 2018.
2
Accumulation of succinate controls activation of adipose tissue thermogenesis.
Nature. 2018 Aug;560(7716):102-106. doi: 10.1038/s41586-018-0353-2. Epub 2018 Jul 18.
3
4
Genetics of Obesity Traits: A Bivariate Genome-Wide Association Analysis.
Front Genet. 2018 May 16;9:179. doi: 10.3389/fgene.2018.00179. eCollection 2018.
5
Enhanced phosphocholine metabolism is essential for terminal erythropoiesis.
Blood. 2018 Jun 28;131(26):2955-2966. doi: 10.1182/blood-2018-03-838516. Epub 2018 Apr 30.
6
SYK kinase mediates brown fat differentiation and activation.
Nat Commun. 2017 Dec 13;8(1):2115. doi: 10.1038/s41467-017-02162-3.
7
Brown Fat AKT2 Is a Cold-Induced Kinase that Stimulates ChREBP-Mediated De Novo Lipogenesis to Optimize Fuel Storage and Thermogenesis.
Cell Metab. 2018 Jan 9;27(1):195-209.e6. doi: 10.1016/j.cmet.2017.10.008. Epub 2017 Nov 16.
10
IL-6 Improves Energy and Glucose Homeostasis in Obesity via Enhanced Central IL-6 trans-Signaling.
Cell Rep. 2017 Apr 11;19(2):267-280. doi: 10.1016/j.celrep.2017.03.043.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验