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1
Commensal bacteria weaken the intestinal barrier by suppressing epithelial neuropilin-1 and Hedgehog signaling.共生菌通过抑制上皮细胞神经纤毛蛋白-1 和 Hedgehog 信号通路来削弱肠道屏障。
Nat Metab. 2023 Jul;5(7):1174-1187. doi: 10.1038/s42255-023-00828-5. Epub 2023 Jul 6.
2
Selected commensals educate the intestinal vascular and immune system for immunocompetence.选定的共生菌可教育肠道血管和免疫系统,以增强免疫能力。
Microbiome. 2022 Sep 28;10(1):158. doi: 10.1186/s40168-022-01353-5.
3
Paneth Cells Regulate Lymphangiogenesis under Control of Microbial Signals during Experimental Portal Hypertension.潘氏细胞在实验性门静脉高压症中微生物信号控制下调节淋巴管生成。
Biomedicines. 2022 Jun 25;10(7):1503. doi: 10.3390/biomedicines10071503.
4
The gut microbiota instructs the hepatic endothelial cell transcriptome.肠道微生物群指导肝内皮细胞转录组。
iScience. 2021 Sep 10;24(10):103092. doi: 10.1016/j.isci.2021.103092. eCollection 2021 Oct 22.
5
Impact of healthy aging on active bacterial assemblages throughout the gastrointestinal tract.健康老龄化对整个胃肠道活跃细菌组合的影响。
Gut Microbes. 2021 Jan-Dec;13(1):1966261. doi: 10.1080/19490976.2021.1966261.
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Enterically derived high-density lipoprotein restrains liver injury through the portal vein.肠源高密度脂蛋白通过门静脉抑制肝损伤。
Science. 2021 Jul 23;373(6553). doi: 10.1126/science.abe6729.
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FOXC2 controls adult lymphatic endothelial specialization, function, and gut lymphatic barrier preventing multiorgan failure.FOXC2 控制成人淋巴管内皮细胞的特化、功能和肠道淋巴管屏障,防止多器官衰竭。
Sci Adv. 2021 Jul 16;7(29). doi: 10.1126/sciadv.abf4335. Print 2021 Jul.
8
The Interplay between Nutrition, Innate Immunity, and the Commensal Microbiota in Adaptive Intestinal Morphogenesis.营养、先天免疫和共生微生物群在适应性肠道形态发生中的相互作用。
Nutrients. 2021 Jun 26;13(7):2198. doi: 10.3390/nu13072198.
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Developmental trajectory of the healthy human gut microbiota during the first 5 years of life.健康人类肠道微生物群在生命最初5年的发育轨迹。
Cell Host Microbe. 2021 May 12;29(5):765-776.e3. doi: 10.1016/j.chom.2021.02.021. Epub 2021 Mar 31.
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A philosophical perspective on the prenatal in utero microbiome debate.对产前子宫内微生物组争论的哲学思考。
Microbiome. 2021 Jan 12;9(1):5. doi: 10.1186/s40168-020-00979-7.

肠道微生物群与微血管。

Gut Microbiota and the Microvasculature.

机构信息

Center for Thrombosis and Hemostasis (CTH), Partner Site Rhine Main, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

German Center for Cardiovascular Research (DZHK), Partner Site Rhine Main, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany.

出版信息

Cold Spring Harb Perspect Med. 2023 Aug 1;13(8):a041179. doi: 10.1101/cshperspect.a041179.

DOI:10.1101/cshperspect.a041179
PMID:37460157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10411863/
Abstract

The gut microbiota is increasingly recognized as an actuating variable shaping vascular development and endothelial cell function in the intestinal mucosa but also affecting the microvasculature of remote organs. In the small intestine, colonization with gut microbiota and subsequent activation of innate immune pathways promotes the development of intricate capillary networks and lacteals, influencing the integrity of the gut-vascular barrier as well as nutrient uptake. Since the liver yields most of its blood supply via the portal circulation, the hepatic microcirculation steadily encounters microbiota-derived patterns and active signaling metabolites that induce changes in the organization of the liver sinusoidal endothelium, influencing immune zonation of sinusoids and impacting on metabolic processes. In addition, microbiota-derived signals may affect the vasculature of distant organ systems such as the brain and the eye microvasculature. In recent years, this gut-resident microbial ecosystem was revealed to contribute to the development of several vascular disease phenotypes.

摘要

肠道微生物群越来越被认为是一种调节变量,它可以塑造肠道黏膜中的血管发育和内皮细胞功能,同时也影响远程器官的微血管。在小肠中,肠道微生物群的定植和随后的先天免疫途径的激活促进了复杂毛细血管网络和乳糜管的发育,影响了肠道-血管屏障的完整性和营养物质的摄取。由于肝脏通过门静脉循环提供其大部分血液供应,因此肝微循环不断遇到来自微生物群的模式和活性信号代谢物,这些物质诱导肝窦内皮细胞的组织结构发生变化,影响窦的免疫分区,并影响代谢过程。此外,微生物群衍生的信号可能会影响大脑和眼睛微血管等远处器官系统的血管。近年来,这一常驻肠道微生物生态系统被揭示有助于几种血管疾病表型的发展。