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
Medway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Division of Experimental Allergology and Immunodermatology, University of Oldenburg, Oldenburg, Germany.
Front Immunol. 2020 Nov 20;11:580557. doi: 10.3389/fimmu.2020.580557. eCollection 2020.
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.
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。