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Autophagy-related protein PIK3C3/VPS34 controls T cell metabolism and function: PIK3C3/VPS34 in T cell metabolism and function

机译:与自噬相关的蛋白Pik3C3 / VPS34控制T细胞代谢和功能:PIK3C3 / VPS34在T细胞代谢和功能中

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摘要

The PIK3C3/VPS34 subunit of the class III phosphatidylinositol 3-kinase (PtdIns3K) complex is a key early player in macroautophagy/autophagy. In this study, we assessed the contribution of PIK3C3 to T cell metabolism and function. We found that Pik3c3-deficient T cells exhibited impaired cellular metabolism, and Pik3c3-deficient CD4+ T cells failed to differentiate into T helper 1 cells. These alterations were associated with reduced levels of active mitochondria upon T cell activation. In addition, conditional Pik3c3-deficient animals failed to mount autoreactive T cell responses and were resistant to experimental autoimmune encephalomyelitis (EAE). Interestingly, the deletion of Pik3c3 had little effect on the capacity of animals to clear tumor metastases. Collectively, our studies have revealed a critical role of PIK3C3 in T cell metabolism and the pathogenicity of these cells during EAE. Our findings also have important implications for the development of immunotherapies to treat multiple sclerosis and other inflammatory diseases by targeting PIK3C3.
机译:III级磷脂酰肌醇3-激酶(PTDINS3K)复合物的PIK3C3 / VPS34亚基是宏观摄影/自噬的关键早期球员。在这项研究中,我们评估了PIK3C3至T细胞代谢和功能的贡献。我们发现Pik3C3缺陷的T细胞表现出损伤的细胞代谢,PIK3C3缺陷的CD4 + T细胞未被分化为T辅助1细胞。这些改变与T细胞活化时的活性线粒体水平降低有关。此外,有条件的Pik3C3缺陷的动物未能安装自动反应性T细胞反应,并对实验性自身免疫脑脊髓炎(EAE)耐药性。有趣的是,Pik3C3的缺失对动物透明肿瘤转移的能力几乎没有影响。集体,我们的研究揭示了PIK3C3在T细胞代谢和在EAE期间这些细胞的致病性的关键作用。我们的调查结果也对靶向PIK3C3来治疗多发性硬化和其他炎症性疾病的免疫治疗免疫治疗的重要意义。

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