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2 型固有淋巴细胞的定位和细胞间的局部相互作用。

Localization and site-specific cell-cell interactions of group 2 innate lymphoid cells.

机构信息

Laboratory for Innate Immune Systems, RIKEN Center for Integrative Medical Sciences (IMS), 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa, Japan.

Laboratory for Innate Immune Systems, Department of Microbiology and Immunology, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka Suita-shi, Osaka, Japan.

出版信息

Int Immunol. 2021 Apr 22;33(5):251-259. doi: 10.1093/intimm/dxab001.

Abstract

Group 2 innate lymphoid cells (ILC2s) are novel lymphocytes discovered in 2010. Unlike T or B cells, ILC2s are activated non-specifically by environmental factors and produce various cytokines, thus playing a role in tissue homeostasis, diseases including allergic diseases, and parasite elimination. ILC2s were first reported as cells abundantly present in fat-associated lymphoid clusters in adipose tissue. However, subsequent studies revealed their presence in various tissues throughout the body, acting as key players in tissue-specific diseases. Recent histologic analyses revealed that ILC2s are concentrated in specific regions in tissues, such as the lamina propria and perivascular regions, with their function being controlled by the surrounding cells, such as epithelial cells and other immune cells, via cytokine and lipid production or by cell-cell interactions through surface molecules. Especially, some stromal cells have been identified as the niche cells for ILC2s, both in the steady state and under inflammatory conditions, through the production of IL-33 or extracellular matrix factors. Additionally, peripheral neurons reportedly co-localize with ILC2s and alter their function directly through neurotransmitters. These findings suggest that the different localizations or different cell-cell interactions might affect the function of ILC2s. Furthermore, generally, ILC2s are thought to be tissue-resident cells; however, they occasionally migrate to other tissues and perform a new role; this supports the importance of the microenvironment for their function. We summarize here the current understanding of how the microenvironment controls ILC2 localization and function with the aim of promoting the development of novel diagnostic and therapeutic methods.

摘要

2 型固有淋巴细胞(ILC2)是 2010 年发现的一种新型淋巴细胞。与 T 或 B 细胞不同,ILC2 被环境因素非特异性激活,并产生各种细胞因子,从而在组织稳态、过敏等疾病和寄生虫清除中发挥作用。ILC2 最初被报道为大量存在于脂肪组织中脂肪相关淋巴簇的细胞。然而,随后的研究表明它们存在于全身各种组织中,作为组织特异性疾病的关键参与者。最近的组织学分析表明,ILC2 集中存在于组织的特定区域,如固有层和血管周围区域,其功能受周围细胞(如上皮细胞和其他免疫细胞)通过细胞因子和脂质产生或通过表面分子进行细胞间相互作用的控制。特别是,一些基质细胞已被确定为 ILC2 的生态位细胞,无论是在稳态还是炎症条件下,通过产生 IL-33 或细胞外基质因子。此外,据报道,外周神经元与 ILC2 共定位,并通过神经递质直接改变其功能。这些发现表明,不同的定位或不同的细胞间相互作用可能影响 ILC2 的功能。此外,一般来说,ILC2 被认为是组织驻留细胞;然而,它们偶尔会迁移到其他组织并发挥新的作用;这支持了微环境对其功能的重要性。我们在这里总结了微环境控制 ILC2 定位和功能的当前理解,旨在促进新的诊断和治疗方法的发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b196/8060991/8b979fa96ff0/dxab001f0001.jpg

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