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本文引用的文献

1
Paneth-cell-disruption-induced necrotizing enterocolitis in mice requires live bacteria and occurs independently of TLR4 signaling.小鼠中潘氏细胞破坏诱导的坏死性小肠结肠炎需要活细菌,且独立于TLR4信号传导发生。
Dis Model Mech. 2017 Jun 1;10(6):727-736. doi: 10.1242/dmm.028589. Epub 2017 Apr 27.
2
Functional Transcriptomics in Diverse Intestinal Epithelial Cell Types Reveals Robust MicroRNA Sensitivity in Intestinal Stem Cells to Microbial Status.不同肠道上皮细胞类型中的功能转录组学揭示了肠道干细胞对微生物状态具有强大的微小RNA敏感性。
J Biol Chem. 2017 Feb 17;292(7):2586-2600. doi: 10.1074/jbc.M116.770099. Epub 2017 Jan 4.
3
Roles for Intestinal Bacteria, Viruses, and Fungi in Pathogenesis of Inflammatory Bowel Diseases and Therapeutic Approaches.肠道细菌、病毒和真菌在炎症性肠病发病机制中的作用及治疗方法
Gastroenterology. 2017 Feb;152(2):327-339.e4. doi: 10.1053/j.gastro.2016.10.012. Epub 2016 Oct 18.
4
Paneth Cell Alterations in the Development and Phenotype of Crohn's Disease.克罗恩病发展过程中的潘氏细胞改变及其表型
Gastroenterology. 2017 Feb;152(2):322-326. doi: 10.1053/j.gastro.2016.10.003. Epub 2016 Oct 8.
5
Paneth cell defects in Crohn's disease patients promote dysbiosis.克罗恩病患者的潘氏细胞缺陷促进了菌群失调。
JCI Insight. 2016 Jun 2;1(8):e86907. doi: 10.1172/jci.insight.86907.
6
The microbiota in adaptive immune homeostasis and disease.适应性免疫稳态和疾病中的微生物组。
Nature. 2016 Jul 7;535(7610):75-84. doi: 10.1038/nature18848.
7
GI stem cells - new insights into roles in physiology and pathophysiology.胃肠道干细胞——对其在生理和病理生理学中作用的新见解
J Physiol. 2016 Sep 1;594(17):4769-79. doi: 10.1113/JP271663. Epub 2016 Apr 24.
8
Acute Graft-versus-Host Disease: Novel Biological Insights.急性移植物抗宿主病:新的生物学见解
Biol Blood Marrow Transplant. 2016 Jan;22(1):11-6. doi: 10.1016/j.bbmt.2015.10.001. Epub 2015 Oct 26.
9
The Viral Mimetic Polyinosinic:Polycytidylic Acid Alters the Growth Characteristics of Small Intestinal and Colonic Crypt Cultures.病毒模拟物聚肌苷酸:聚胞苷酸改变小肠和结肠隐窝培养物的生长特性。
PLoS One. 2015 Sep 28;10(9):e0138531. doi: 10.1371/journal.pone.0138531. eCollection 2015.
10
SOX9 maintains reserve stem cells and preserves radioresistance in mouse small intestine.SOX9维持小鼠小肠中的储备干细胞并保持放射抗性。
Gastroenterology. 2015 Nov;149(6):1553-1563.e10. doi: 10.1053/j.gastro.2015.07.004. Epub 2015 Jul 11.

肠内微生物群调节空肠潘氏细胞数量和功能,而不影响肠道干细胞。

The enteric microbiota regulates jejunal Paneth cell number and function without impacting intestinal stem cells.

机构信息

a Center for Gastrointestinal Biology and Disease , University of North Carolina at Chapel Hill , Chapel Hill , NC 27599 , USA.

b Department of Pediatrics, Division of Gastroenterology , University of North Carolina at Chapel Hill , Chapel Hill , NC 27599 , USA.

出版信息

Gut Microbes. 2019;10(1):45-58. doi: 10.1080/19490976.2018.1474321. Epub 2018 Jul 11.

DOI:10.1080/19490976.2018.1474321
PMID:29883265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6363071/
Abstract

Paneth cells (PCs) are epithelial cells found in the small intestine, next to intestinal stem cells (ISCs) at the base of the crypts. PCs secrete antimicrobial peptides (AMPs) that regulate the commensal gut microbiota. In contrast, little is known regarding how the enteric microbiota reciprocally influences PC function. In this study, we sought to characterize the impact of the enteric microbiota on PC biology in the mouse small intestine. This was done by first enumerating jejunal PCs in germ-free (GF) versus conventionally raised (CR) mice. We next evaluated the possible functional consequences of altered PC biology in these experimental groups by assessing epithelial proliferation, ISC numbers, and the production of AMPs. We found that PC numbers were significantly increased in CR versus GF mice; however, there were no differences in ISC numbers or cycling activity between groups. Of the AMPs assessed, only Reg3γ transcript expression was significantly increased in CR mice. Intriguingly, this increase was abrogated in cultured CR versus GF enteroids, and could not be re-induced with various bacterial ligands. Our findings demonstrate the enteric microbiota regulates PC function by increasing PC numbers and inducing Reg3γ expression, though the latter effect may not involve direct interactions between bacteria and the intestinal epithelium. In contrast, the enteric microbiota does not appear to regulate jejunal ISC census and proliferation. These are critical findings for investigators using GF mice and the enteroid system to study PC and ISC biology.

摘要

潘氏细胞(PCs)是位于小肠中的上皮细胞,位于隐窝底部的肠干细胞(ISCs)旁边。PCs 分泌抗菌肽(AMPs),调节共生肠道微生物群。相比之下,对于肠道微生物群如何反过来影响 PC 功能,人们知之甚少。在这项研究中,我们试图描述肠道微生物群对小鼠小肠中 PC 生物学的影响。这是通过首先在无菌(GF)和常规饲养(CR)小鼠中计数空肠 PCs 来完成的。接下来,我们通过评估上皮细胞增殖、ISCs 数量和 AMP 产生来评估这些实验组中 PC 生物学改变的可能功能后果。我们发现,CR 小鼠中的 PC 数量明显高于 GF 小鼠;然而,两组间 ISC 数量或细胞周期活性无差异。在所评估的 AMP 中,只有 Reg3γ 转录物的表达在 CR 小鼠中显著增加。有趣的是,这种增加在培养的 CR 与 GF 类肠上皮细胞中被消除,并且不能用各种细菌配体重新诱导。我们的研究结果表明,肠道微生物群通过增加 PC 数量和诱导 Reg3γ 表达来调节 PC 功能,尽管后者的作用可能不涉及细菌与肠上皮之间的直接相互作用。相比之下,肠道微生物群似乎不调节空肠 ISC 计数和增殖。这些发现对于使用 GF 小鼠和类肠上皮细胞系统研究 PC 和 ISC 生物学的研究人员来说是至关重要的。