Suppr超能文献

健康和致动脉粥样硬化条件下跨器官的代谢物生成与消耗

Cross-organ metabolite production and consumption in healthy and atherogenic conditions.

作者信息

Bae Hosung, Jung Sunhee, Le Johnny, Tamburini Ian, Kim Joohwan, Wang Eric, Song Won-Suk, Choi Wonsuk, Jang Ki-Hong, Kang Taekyung, Lopez Miranda L, Ramirez Cuauhtemoc, Mohanty Ipsita, Kelly Miranda E, Kim Jessie, Kim Raymond, Park Sang Hee, Baek Jongwon, Mendez Bryan, Petrus Paul, de Aguiar Vallim Thomas Q, Nicholas Dequina A, Smith Quinton, Lee Gina, Seldin Marcus, Jang Cholsoon

机构信息

Department of Biological Chemistry, University of California, Irvine, Irvine, CA, USA.

Department of Microbiology and Molecular Genetics, University of California, Irvine, Irvine, CA, USA.

出版信息

Cell. 2025 Aug 7;188(16):4441-4455.e16. doi: 10.1016/j.cell.2025.05.001. Epub 2025 May 27.

Abstract

Mammalian organs continuously produce and consume circulating metabolites for organismal health and survival. However, the landscape of this fundamental process and its perturbation by diet and disease is unknown. Using arteriovenous metabolomics, tissue transcriptomics, and hormone arrays in multiple pathophysiological conditions in pigs, we generated an atlas of 10 cross-organ metabolite production and consumption during fasting/feeding, Western diet, and cardiovascular disease progression induced by low-density lipoprotein receptor (LDLR) deficiency. We discovered numerous instances of feeding-dependent and -independent metabolite production and consumption by organs and proposed mechanisms by which these are disrupted by Western diet via altered metabolite concentration gradients and hormones. Both Western diet and LDLR deficiency trigger the release of bile acids (BAs) by extra-hepatic organs, likely contributing to abnormally elevated circulating BA levels and consequent vascular inflammation and atherosclerosis development. These resources reveal intricate inter-organ metabolic crosstalk across pathophysiological conditions, offering biochemical insights into diet effects and cardiometabolic diseases.

摘要

哺乳动物的器官持续产生和消耗循环代谢物以维持机体健康和生存。然而,这一基本过程的全貌以及饮食和疾病对其的干扰尚不清楚。我们利用猪在多种病理生理条件下的动静脉代谢组学、组织转录组学和激素阵列,生成了一份在禁食/进食、西式饮食以及由低密度脂蛋白受体(LDLR)缺乏引起的心血管疾病进展过程中10种跨器官代谢物产生和消耗的图谱。我们发现了许多器官依赖进食和不依赖进食的代谢物产生和消耗的实例,并提出了西式饮食通过改变代谢物浓度梯度和激素来破坏这些过程的机制。西式饮食和LDLR缺乏都会触发肝外器官释放胆汁酸(BAs),这可能导致循环中BA水平异常升高,进而引发血管炎症和动脉粥样硬化。这些资源揭示了病理生理条件下复杂的器官间代谢串扰,为饮食影响和心脏代谢疾病提供了生化见解。

相似文献

1
Cross-organ metabolite production and consumption in healthy and atherogenic conditions.
Cell. 2025 Aug 7;188(16):4441-4455.e16. doi: 10.1016/j.cell.2025.05.001. Epub 2025 May 27.
3
Metabolite Exchange between Mammalian Organs Quantified in Pigs.
Cell Metab. 2019 Sep 3;30(3):594-606.e3. doi: 10.1016/j.cmet.2019.06.002. Epub 2019 Jun 27.
5
Endothelial Stiffening Induced by CD36-Mediated Lipid Uptake Leads to Endothelial Barrier Disruption and Contributes to Atherosclerotic Lesions.
Arterioscler Thromb Vasc Biol. 2025 Jun;45(6):e201-e216. doi: 10.1161/ATVBAHA.124.322244. Epub 2025 Apr 10.
8
Ertugliflozin attenuates atherosclerosis in nondiabetic ApoE mice by upregulating ABCA1 and LDLR via the PPARγ/LXRα pathway.
Biochim Biophys Acta Mol Basis Dis. 2025 Oct;1871(7):167927. doi: 10.1016/j.bbadis.2025.167927. Epub 2025 May 24.

本文引用的文献

1
Enterococcal-host interactions in the gastrointestinal tract and beyond.
FEMS Microbes. 2024 Sep 9;5:xtae027. doi: 10.1093/femsmc/xtae027. eCollection 2024.
2
A brief harvesting-freezing delay significantly alters the kidney metabolome and leads to false positive and negative results.
Am J Physiol Renal Physiol. 2024 Nov 1;327(5):F697-F711. doi: 10.1152/ajprenal.00131.2024. Epub 2024 Aug 29.
4
Clostridial Myonecrosis: A Comprehensive Review of Toxin Pathophysiology and Management Strategies.
Microorganisms. 2024 Jul 18;12(7):1464. doi: 10.3390/microorganisms12071464.
5
Arteriovenous metabolomics in pigs reveals CFTR regulation of metabolism in multiple organs.
J Clin Invest. 2024 May 14;134(13):e174500. doi: 10.1172/JCI174500.
6
Gut symbionts alleviate MASH through a secondary bile acid biosynthetic pathway.
Cell. 2024 May 23;187(11):2717-2734.e33. doi: 10.1016/j.cell.2024.03.034. Epub 2024 Apr 22.
7
Intestinal FGF15 regulates bile acid and cholesterol metabolism but not glucose and energy balance.
JCI Insight. 2024 Apr 8;9(7):e174164. doi: 10.1172/jci.insight.174164.
8
The changing metabolic landscape of bile acids - keys to metabolism and immune regulation.
Nat Rev Gastroenterol Hepatol. 2024 Jul;21(7):493-516. doi: 10.1038/s41575-024-00914-3. Epub 2024 Apr 4.
9
Cardiometabolic characteristics of people with metabolically healthy and unhealthy obesity.
Cell Metab. 2024 Apr 2;36(4):745-761.e5. doi: 10.1016/j.cmet.2024.03.002.
10
Neuroactive metabolites and bile acids are altered in extremely premature infants with brain injury.
Cell Rep Med. 2024 Apr 16;5(4):101480. doi: 10.1016/j.xcrm.2024.101480. Epub 2024 Mar 22.

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