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中性粒细胞表达的 CD47 调节体内肠道中 CD11b/CD18 依赖性中性粒细胞跨上皮迁移。

Neutrophil expressed CD47 regulates CD11b/CD18-dependent neutrophil transepithelial migration in the intestine in vivo.

机构信息

Department of Pathology, University of Michigan School of Medicine, Ann Arbor, MI, 48109, USA.

Center for Excellence in Vascular Biology, Department of Pathology, Brigham and Women's Hospital, Boston, MA, 02115, USA.

出版信息

Mucosal Immunol. 2021 Mar;14(2):331-341. doi: 10.1038/s41385-020-0316-4. Epub 2020 Jun 19.

Abstract

Dysregulated neutrophil (PMN) transmigration across epithelial surfaces (TEpM) significantly contributes to chronic inflammatory diseases, yet mechanisms defining this process remain poorly understood. In the intestine, uncontrolled PMN TEpM is a hallmark of disease flares in ulcerative colitis. Previous in vitro studies directed at identifying molecular determinants that mediate TEpM have shown that plasma membrane proteins including CD47 and CD11b/CD18 play key roles in regulating PMN TEpM across monolayers of intestinal epithelial cells. Here, we show that CD47 modulates PMN TEpM in vivo using an ileal loop assay. Importantly, using novel tissue-specific CD47 knockout mice and in vitro approaches, we report that PMN-expressed, but not epithelial-expressed CD47 plays a major role in regulating PMN TEpM. We show that CD47 associates with CD11b/CD18 in the plasma membrane of PMN, and that loss of CD47 results in impaired CD11b/CD18 activation. In addition, in vitro and in vivo studies using function blocking antibodies support a role of CD47 in regulating CD11b-dependent PMN TEpM and chemotaxis. Taken together, these findings provide new insights for developing approaches to target dysregulated PMN infiltration in the intestine. Moreover, tissue-specific CD47 knockout mice constitute an important new tool to study contributions of cells expressing CD47 to inflammation in vivo.

摘要

中性粒细胞(PMN)跨上皮表面迁移(TEpM)的失调显著促进了慢性炎症性疾病的发生,但定义这一过程的机制仍知之甚少。在肠道中,不受控制的 PMN TEpM 是溃疡性结肠炎疾病发作的标志。以前的体外研究旨在确定介导 TEpM 的分子决定因素,表明包括 CD47 和 CD11b/CD18 在内的质膜蛋白在调节 PMN 跨肠道上皮细胞单层的 TEpM 中发挥关键作用。在这里,我们使用回肠环试验显示 CD47 可调节体内 PMN TEpM。重要的是,使用新型组织特异性 CD47 敲除小鼠和体外方法,我们报告说 PMN 表达的而不是上皮细胞表达的 CD47 在调节 PMN TEpM 中起着主要作用。我们表明 CD47 在 PMN 的质膜中与 CD11b/CD18 相关,并且 CD47 的缺失导致 CD11b/CD18 激活受损。此外,使用功能阻断抗体的体外和体内研究支持 CD47 在调节 CD11b 依赖性 PMN TEpM 和趋化作用中的作用。总之,这些发现为开发针对肠道中失调的 PMN 浸润的方法提供了新的见解。此外,组织特异性 CD47 敲除小鼠构成了研究体内表达 CD47 的细胞对炎症贡献的重要新工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3631/7749029/0fc70cc92aec/nihms-1601520-f0001.jpg

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