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鉴定、分离和分析人类肠道相关淋巴组织。

Identification, isolation and analysis of human gut-associated lymphoid tissues.

机构信息

Department of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.

Department of Pathology, Herlev Hospital, University of Copenhagen, Herlev, Denmark.

出版信息

Nat Protoc. 2021 Apr;16(4):2051-2067. doi: 10.1038/s41596-020-00482-1. Epub 2021 Feb 22.

Abstract

Gut-associated lymphoid tissues (GALTs) comprise key intestinal immune inductive sites, including the Peyer's patches of the small intestine and different types of isolated lymphoid follicle (ILF) found along the length of the gut. Our understanding of human GALT is limited due to a lack of protocols for their isolation. Here we describe a technique that, uniquely among intestinal cell isolation protocols, allows identification and isolation of all human GALT, as well as GALT-free intestinal lamina propria (LP). The technique involves the mechanical separation of intestinal mucosa from the submucosa, allowing the identification and isolation of submucosal ILF (SM-ILF), LP-embedded mucosal ILF (M-ILF) and LP free of contaminating lymphoid tissue. Individual SM-ILF, M-ILF and Peyer's patch follicles can be subsequently digested for downstream cellular and molecular characterization. The technique, which takes 4-10 h, will be useful for researchers interested in intestinal immune development and function in health and disease.

摘要

肠相关淋巴组织(GALTs)包括关键的肠道免疫诱导部位,包括小肠的派尔集合淋巴结和沿着肠道全长发现的不同类型的孤立淋巴滤泡(ILF)。由于缺乏其分离的方案,我们对人类 GALT 的了解受到限制。在这里,我们描述了一种技术,该技术在肠道细胞分离方案中是独一无二的,可用于鉴定和分离所有人类 GALT 以及无 GALT 的肠道固有层(LP)。该技术涉及从黏膜下层机械分离肠黏膜,允许鉴定和分离黏膜下层 ILF(SM-ILF)、嵌入 LP 的黏膜 ILF(M-ILF)和无污染淋巴组织的 LP。随后可以对单个 SM-ILF、M-ILF 和派尔集合淋巴结滤泡进行消化,以进行下游细胞和分子特征分析。该技术耗时 4-10 小时,对于有兴趣研究肠道免疫在健康和疾病中的发育和功能的研究人员将非常有用。

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