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本文引用的文献

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Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes.先天性巨结肠症——整合基础科学和临床医学以改善治疗效果。
Nat Rev Gastroenterol Hepatol. 2018 Mar;15(3):152-167. doi: 10.1038/nrgastro.2017.149. Epub 2018 Jan 4.
2
Adult enteric nervous system in health is maintained by a dynamic balance between neuronal apoptosis and neurogenesis.健康状态下,成人的肠神经系统通过神经元凋亡与神经发生之间的动态平衡得以维持。
Proc Natl Acad Sci U S A. 2017 May 2;114(18):E3709-E3718. doi: 10.1073/pnas.1619406114. Epub 2017 Apr 18.
3
Glial-cell-derived neuroregulators control type 3 innate lymphoid cells and gut defence.神经胶质细胞衍生的神经调节因子控制3型天然淋巴细胞和肠道防御。
Nature. 2016 Jul 21;535(7612):440-443. doi: 10.1038/nature18644. Epub 2016 Jul 13.
4
Gene-environment interactions and the enteric nervous system: Neural plasticity and Hirschsprung disease prevention.基因-环境相互作用与肠神经系统:神经可塑性与先天性巨结肠的预防
Dev Biol. 2016 Sep 15;417(2):188-97. doi: 10.1016/j.ydbio.2016.03.017. Epub 2016 Mar 17.
5
Established and emerging concepts in Hirschsprung's-associated enterocolitis.先天性巨结肠相关小肠结肠炎的既定概念与新出现的概念。
Pediatr Surg Int. 2016 Apr;32(4):313-20. doi: 10.1007/s00383-016-3862-9. Epub 2016 Jan 19.
6
Neuro-immune Interactions Drive Tissue Programming in Intestinal Macrophages.神经免疫相互作用驱动肠道巨噬细胞中的组织编程。
Cell. 2016 Jan 28;164(3):378-91. doi: 10.1016/j.cell.2015.12.023. Epub 2016 Jan 14.
7
Ibuprofen slows migration and inhibits bowel colonization by enteric nervous system precursors in zebrafish, chick and mouse.布洛芬可减缓斑马鱼、鸡和小鼠中肠神经系统前体细胞的迁移并抑制其在肠道的定植。
Dev Biol. 2016 Jan 15;409(2):473-88. doi: 10.1016/j.ydbio.2015.09.023. Epub 2015 Nov 14.
8
Neural crest requires Impdh2 for development of the enteric nervous system, great vessels, and craniofacial skeleton.神经嵴发育肠神经系统、大血管和颅面骨骼需要肌苷-5'-单磷酸脱氢酶2(Impdh2)。
Dev Biol. 2016 Jan 1;409(1):152-165. doi: 10.1016/j.ydbio.2015.11.004. Epub 2015 Nov 10.
9
Hepatocyte Growth Factor and MET Support Mouse Enteric Nervous System Development, the Peristaltic Response, and Intestinal Epithelial Proliferation in Response to Injury.肝细胞生长因子和MET支持小鼠肠道神经系统发育、蠕动反应以及肠道上皮对损伤的增殖反应。
J Neurosci. 2015 Aug 19;35(33):11543-58. doi: 10.1523/JNEUROSCI.5267-14.2015.
10
Purification of dendritic cell and macrophage subsets from the normal mouse small intestine.从正常小鼠小肠中纯化树突状细胞和巨噬细胞亚群。
J Immunol Methods. 2015 Jun;421:1-13. doi: 10.1016/j.jim.2015.02.013. Epub 2015 Mar 18.

肌层巨噬细胞在没有肠神经系统的情况下的发育。

Muscularis macrophage development in the absence of an enteric nervous system.

机构信息

Abramson Research Center, The Children's Hospital of Philadelphia Research Institute, Philadelphia, PA 19104-4318.

Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104.

出版信息

Proc Natl Acad Sci U S A. 2018 May 1;115(18):4696-4701. doi: 10.1073/pnas.1802490115. Epub 2018 Apr 17.

DOI:10.1073/pnas.1802490115
PMID:29666241
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5939112/
Abstract

The nervous system of the bowel regulates the inflammatory phenotype of tissue resident muscularis macrophages (MM), and in adult mice, enteric neurons are the main local source of colony stimulating factor 1 (CSF1), a protein required for MM survival. Surprisingly, we find that during development MM colonize the bowel before enteric neurons. This calls into question the requirement for neuron-derived CSF1 for MM colonization of the bowel. To determine if intestinal innervation is required for MM development, we analyzed MM of neonatal ( KO) mice that have no enteric nervous system in small bowel or colon. We found normal numbers of well-patterned MM in KO bowel. Similarly, the abundance and distribution of MM in aganglionic human colon obtained from Hirschsprung disease patients was normal. We also identify endothelial cells and interstitial cells of Cajal as the main sources of in the developing bowel. Additionally, MM from neonatal KOs do not differ from controls in baseline activation status or cytokine-production in response to lipopolysaccharide. Unexpectedly, these data demonstrate that the enteric nervous system is dispensable for MM colonization and patterning in the bowel, and suggest that modulatory interactions between MM and the bowel nervous system are established postnatally.

摘要

肠道的神经系统调节组织驻留的肌间巨噬细胞(MM)的炎症表型,在成年小鼠中,肠神经元是集落刺激因子 1(CSF1)的主要局部来源,CSF1 是 MM 存活所必需的蛋白。令人惊讶的是,我们发现 MM 在肠神经元之前定植于肠道的发育过程中。这就提出了一个问题,即神经元衍生的 CSF1 是否是 MM 定植于肠道所必需的。为了确定肠神经支配是否是 MM 发育所必需的,我们分析了新生(KO)小鼠的 MM,这些小鼠的小肠或结肠中没有肠神经系统。我们发现 KO 小鼠的肠道中存在正常数量的 MM。同样,从先天性巨结肠症患者获得的无神经节的人类结肠中 MM 的丰度和分布也正常。我们还确定了内皮细胞和 Cajal 间质细胞是发育中肠道中 CSF1 的主要来源。此外,与对照组相比,来自新生 KO 小鼠的 MM 在脂多糖刺激下的基础激活状态或细胞因子产生方面没有差异。出乎意料的是,这些数据表明,肠神经系统对于 MM 定植和肠道模式化是可有可无的,并且提示 MM 和肠道神经系统之间的调节相互作用是在出生后建立的。