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半乳糖凝集素-9与VISTA的配体-受体相互作用抑制人类T淋巴细胞的细胞毒性活性。

Ligand-Receptor Interactions of Galectin-9 and VISTA Suppress Human T Lymphocyte Cytotoxic Activity.

作者信息

Yasinska Inna M, Meyer N Helge, Schlichtner Stephanie, Hussain Rohanah, Siligardi Giuliano, Casely-Hayford Maxwell, Fiedler Walter, Wellbrock Jasmin, Desmet Cloe, Calzolai Luigi, Varani Luca, Berger Steffen M, Raap Ulrike, Gibbs Bernhard F, Fasler-Kan Elizaveta, Sumbayev Vadim V

机构信息

Medway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.

Division of Experimental Allergology and Immunodermatology, University of Oldenburg, Oldenburg, Germany.

出版信息

Front Immunol. 2020 Nov 20;11:580557. doi: 10.3389/fimmu.2020.580557. eCollection 2020.

Abstract

Acute myeloid leukemia (AML), a blood/bone marrow cancer, is a severe and often fatal malignancy. AML cells are capable of impairing the anti-cancer activities of cytotoxic lymphoid cells. This includes the inactivation of natural killer (NK) cells and killing of T lymphocytes. Here we report for the first time that V-domain Ig-containing suppressor of T cell activation (VISTA), a protein expressed by T cells, recognizes galectin-9 secreted by AML cells as a ligand. Importantly, we found that soluble VISTA released by AML cells enhances the effect of galectin-9, most likely by forming multiprotein complexes on the surface of T cells and possibly creating a molecular barrier. These events cause changes in the plasma membrane potential of T cells leading to activation of granzyme B inside cytotoxic T cells, resulting in apoptosis.

摘要

急性髓系白血病(AML)是一种血液/骨髓癌症,是一种严重且通常致命的恶性肿瘤。AML细胞能够损害细胞毒性淋巴细胞的抗癌活性。这包括自然杀伤(NK)细胞的失活和T淋巴细胞的杀伤。在此,我们首次报告T细胞表达的一种蛋白质——含V结构域的T细胞激活抑制因子(VISTA),将AML细胞分泌的半乳凝素-9识别为配体。重要的是,我们发现AML细胞释放的可溶性VISTA增强了半乳凝素-9的作用,很可能是通过在T细胞表面形成多蛋白复合物,并可能形成分子屏障。这些事件导致T细胞膜电位发生变化,从而导致细胞毒性T细胞内颗粒酶B的激活,进而导致细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a818/7715031/1d8117d261c5/fimmu-11-580557-g001.jpg

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