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固有淋巴细胞的组织依赖性适应性和功能。

Tissue-Dependent Adaptations and Functions of Innate Lymphoid Cells.

机构信息

Department of Immunology, University of Toronto, Toronto, ON, Canada.

Toronto General Hospital Research Institute, University Health Network, Toronto, ON, Canada.

出版信息

Front Immunol. 2022 Mar 10;13:836999. doi: 10.3389/fimmu.2022.836999. eCollection 2022.


DOI:10.3389/fimmu.2022.836999
PMID:35359972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8960279/
Abstract

Tissue-resident immune cells reside in distinct niches across organs, where they contribute to tissue homeostasis and rapidly respond to perturbations in the local microenvironment. Innate lymphoid cells (ILCs) are a family of innate immune cells that regulate immune and tissue homeostasis. Across anatomical locations throughout the body, ILCs adopt tissue-specific fates, differing from circulating ILC populations. Adaptations of ILCs to microenvironmental changes have been documented in several inflammatory contexts, including obesity, asthma, and inflammatory bowel disease. While our understanding of ILC functions within tissues have predominantly been based on mouse studies, development of advanced single cell platforms to study tissue-resident ILCs in humans and emerging patient-based data is providing new insights into this lymphocyte family. Within this review, we discuss current concepts of ILC fate and function, exploring tissue-specific functions of ILCs and their contribution to health and disease across organ systems.

摘要

组织驻留免疫细胞存在于器官内的不同龛位,在那里它们有助于组织的稳态,并能迅速响应局部微环境的干扰。固有淋巴细胞(ILC)是一类先天免疫细胞,它们调节免疫和组织稳态。在全身的解剖位置上,ILC 采用组织特异性命运,与循环 ILC 群体不同。在几种炎症情况下,包括肥胖、哮喘和炎症性肠病,已经记录了 ILC 对微环境变化的适应。虽然我们对 ILC 在组织内的功能的理解主要基于小鼠研究,但开发先进的单细胞平台来研究人类组织驻留的 ILC 和新兴的基于患者的数据正在为这个淋巴细胞家族提供新的见解。在这篇综述中,我们讨论了 ILC 命运和功能的当前概念,探讨了 ILC 的组织特异性功能及其对不同器官系统健康和疾病的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/8d40fec9f84a/fimmu-13-836999-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/71444c424cdc/fimmu-13-836999-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/cb58eff2cb5d/fimmu-13-836999-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/b7373b6b0e1a/fimmu-13-836999-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/9e6c0e6b88be/fimmu-13-836999-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/bcefe7fb79e9/fimmu-13-836999-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/4546b64b4ef0/fimmu-13-836999-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/e66f5671c05f/fimmu-13-836999-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/af9fa84107c8/fimmu-13-836999-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/162657ddd81f/fimmu-13-836999-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/bae4446d6dea/fimmu-13-836999-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/8d40fec9f84a/fimmu-13-836999-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/71444c424cdc/fimmu-13-836999-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/cb58eff2cb5d/fimmu-13-836999-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/b7373b6b0e1a/fimmu-13-836999-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/9e6c0e6b88be/fimmu-13-836999-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/bcefe7fb79e9/fimmu-13-836999-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/4546b64b4ef0/fimmu-13-836999-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/e66f5671c05f/fimmu-13-836999-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/af9fa84107c8/fimmu-13-836999-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/162657ddd81f/fimmu-13-836999-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/bae4446d6dea/fimmu-13-836999-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b49/8960279/8d40fec9f84a/fimmu-13-836999-g011.jpg

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本文引用的文献

[1]
IL-33 activates group 2 innate lymphoid cell expansion and modulates endometriosis.

JCI Insight. 2021-12-8

[2]
Vasoactive intestinal peptide promotes host defense against enteric pathogens by modulating the recruitment of group 3 innate lymphoid cells.

Proc Natl Acad Sci U S A. 2021-10-12

[3]
CD127+ CD94+ innate lymphoid cells expressing granulysin and perforin are expanded in patients with Crohn's disease.

Nat Commun. 2021-10-6

[4]
Searching for the Elusive Regulatory Innate Lymphoid Cell.

J Immunol. 2021-10-15

[5]
Reduced innate lymphoid cells in the endometrium of women with endometriosis.

Am J Reprod Immunol. 2022-1

[6]
Innate Lymphoid Cells Promote Recovery of Ventricular Function After Myocardial Infarction.

J Am Coll Cardiol. 2021-9-14

[7]
Quantification and role of innate lymphoid cell subsets in Chronic Obstructive Pulmonary Disease.

Clin Transl Immunology. 2021-6-5

[8]
GPR34-mediated sensing of lysophosphatidylserine released by apoptotic neutrophils activates type 3 innate lymphoid cells to mediate tissue repair.

Immunity. 2021-6-8

[9]
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