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Diacylglycerol kinase α regulates the formation and polarisation of mature multivesicular bodies involved in the secretion of Fas ligand-containing exosomes in T lymphocytes

机译:二酰基甘油激酶α调节成熟的多囊小体的形成和极化该多囊小体参与T淋巴细胞中含有Fas配体的囊泡的分泌

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摘要

Multivesicular bodies (MVBs) are endocytic compartments that contain intraluminal vesicles formed by inward budding from the limiting membrane of endosomes. In T lymphocytes, these vesicles contain pro-apoptotic Fas ligand (FasL), which may be secreted as ‘lethal exosomes' upon fusion of MVBs with the plasma membrane. Diacylglycerol kinase α (DGKα) regulate the secretion of exosomes, but it is unclear how this control is mediated. T-lymphocyte activation increases the number of MVBs that contain FasL. DGKα is recruited to MVBs and to exosomes in which it has a double function. DGKα kinase activity exerts a negative role in the formation of mature MVBs, as we demonstrate by the use of an inhibitor. Downmodulation of DGKα protein resulted in inhibition of both the polarisation of MVBs towards immune synapse and exosome secretion. The subcellular location of DGKα together with its complex role in the formation and polarised traffic of MVBs support the notion that DGKα is a key regulator of the polarised secretion of exosomes.
机译:多囊泡体(MVB)是内吞的隔室,其中包含腔内囊泡,囊泡是通过从内体的限制膜向内发芽形成的。在T淋巴细胞中,这些囊泡含有促凋亡的Fas配体(FasL),当MVB与质膜融合时,它可能以“致死性外泌体”的形式分泌。二酰基甘油激酶α(DGKα)调节外泌体的分泌,但尚不清楚该调控是如何介导的。 T淋巴细胞激活会增加含有FasL的MVB的数量。 DGKα被募集到MVB和具有双重功能的外泌体中。 DGKα激酶活性在成熟MVB的形成中起着负面作用,正如我们通过使用抑制剂所证明的那样。 DGKα蛋白的下调导致对MVBs向免疫突触的极化和外泌体分泌的抑制。 DGKα的亚细胞位置以及其在MVB的形成和极化运输中的复杂作用,支持了DGKα是外泌体极化分泌的关键调节因子的观点。

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