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膜受体与配体的相互作用。

Interactions of Membrane Receptors and Ligands.

机构信息

Department of Cell and Developmental Biology, University of California, San Diego, La Jolla, California, USA; email:

出版信息

Annu Rev Cell Dev Biol. 2023 Oct 16;39:391-408. doi: 10.1146/annurev-cellbio-120420-103941. Epub 2023 Jun 20.

DOI:10.1146/annurev-cellbio-120420-103941
PMID:37339682
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11734567/
Abstract

Cell-cell communication is critical for the development and function of multicellular organisms. A crucial means by which cells communicate with one another is physical interactions between receptors on one cell and their ligands on a neighboring cell. ligand:receptor interactions activate the receptor, ultimately leading to changes in the fate of the receptor-expressing cells. Such signaling is known to be critical for the functions of cells in the nervous and immune systems, among others. Historically, interactions are the primary conceptual framework for understanding cell-cell communication. However, cells often coexpress many receptors and ligands, and a subset of these has been reported to interact in and profoundly impact cell functions. interactions likely constitute a fundamental, understudied regulatory mechanism in cell biology. Here, I discuss how interactions between membrane receptors and ligands regulate immune cell functions, and I also highlight outstanding questions in the field.

摘要

细胞间通讯对于多细胞生物的发育和功能至关重要。细胞间相互通讯的一个关键手段是相邻细胞上受体与其配体之间的物理相互作用。配体-受体相互作用激活受体,最终导致表达受体的细胞命运发生变化。这种信号传递被认为对神经系统和免疫系统等细胞的功能至关重要。历史上,细胞间相互作用是理解细胞间通讯的主要概念框架。然而,细胞通常共表达许多受体和配体,并且据报道其中一部分以配体-受体相互作用的形式存在,并深刻影响细胞功能。配体-受体相互作用可能构成细胞生物学中一个基本但研究不足的调节机制。在这里,我讨论了膜受体和配体之间的配体-受体相互作用如何调节免疫细胞功能,并且还强调了该领域的一些悬而未决的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/1d6cd7404328/nihms-2044919-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/d70ec9bb30ca/nihms-2044919-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/3e6e633fba43/nihms-2044919-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/ef4e71dfc924/nihms-2044919-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/1d6cd7404328/nihms-2044919-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/d70ec9bb30ca/nihms-2044919-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/3e6e633fba43/nihms-2044919-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/ef4e71dfc924/nihms-2044919-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/962f/11734567/1d6cd7404328/nihms-2044919-f0004.jpg

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本文引用的文献

1
cis-B7:CD28 interactions at invaginated synaptic membranes provide CD28 co-stimulation and promote CD8 T cell function and anti-tumor immunity.内陷突触膜上的 cis-B7:CD28 相互作用提供 CD28 共刺激作用,促进 CD8 T 细胞功能和抗肿瘤免疫。
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CTLA4 depletes T cell endogenous and trogocytosed B7 ligands via cis-endocytosis.CTLA4 通过顺式内吞作用耗竭 T 细胞内源性和转胞吞作用的 B7 配体。
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Differential trafficking of ligands trogocytosed via CD28 versus CTLA4 promotes collective cellular control of co-stimulation.
配体通过 CD28 与 CTLA4 内化后的差异转运促进共刺激的细胞集体控制。
Nat Commun. 2022 Oct 29;13(1):6459. doi: 10.1038/s41467-022-34156-1.
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Cis interactions between CD2 and its ligands on T cells are required for T cell activation.CD2 与其在 T 细胞上的配体之间的顺式相互作用是 T 细胞激活所必需的。
Sci Immunol. 2022 Aug 5;7(74):eabn6373. doi: 10.1126/sciimmunol.abn6373.
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Rapid cloning of antigen-specific T-cell receptors by leveraging the cis activation of T cells.通过利用 T 细胞的顺式激活,快速克隆抗原特异性 T 细胞受体。
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The engineered CD80 variant fusion therapeutic davoceticept combines checkpoint antagonism with conditional CD28 costimulation for anti-tumor immunity.工程化的 CD80 变体融合治疗性药物 davoceticept 将检查点拮抗作用与条件性 CD28 共刺激作用相结合,用于抗肿瘤免疫。
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PD-L1 expression by dendritic cells is a key regulator of T-cell immunity in cancer.树突状细胞的程序性死亡配体1(PD-L1)表达是癌症中T细胞免疫的关键调节因子。
Nat Cancer. 2020 Jul;1(7):681-691. doi: 10.1038/s43018-020-0075-x. Epub 2020 Jun 22.
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Trogocytosis in Unicellular Eukaryotes.单细胞真核生物中的胞饮作用。
Cells. 2021 Nov 1;10(11):2975. doi: 10.3390/cells10112975.
9
Surfing on Membrane Waves: Microvilli, Curved Membranes, and Immune Signaling.在膜波上冲浪:微绒毛、弯曲的膜和免疫信号。
Front Immunol. 2020 Sep 11;11:2187. doi: 10.3389/fimmu.2020.02187. eCollection 2020.
10
A dynamic CD2-rich compartment at the outer edge of the immunological synapse boosts and integrates signals.免疫突触外缘富含 CD2 的动态隔室增强和整合信号。
Nat Immunol. 2020 Oct;21(10):1232-1243. doi: 10.1038/s41590-020-0770-x. Epub 2020 Sep 14.