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Brasilicardin A, a natural immunosuppressant, targets amino acid transport system L

机译:Brasilicardin A(天然免疫抑制剂)靶向氨基酸转运系统L

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Lymphocytes in T cell activation require extracellular nutrients to provide energy for cellular proliferation and effector functions. Therefore, inhibitors of nutrient transporters are expected to be a new class of immunosuppressant. Here, we report that the molecular target of brasilicardin A (BraA), an immunosuppressive compound, is the amino acid transporter system L. BraA inhibited the cell-cycle progression of murine T cell lymphocyte CTLL-2 cells in G1 phase, and potently inhibited the uptake of amino acids that are substrates for amino acid transport system L. Moreover, BraA stimulated the GCN2 activation and, subsequently, the phosphorylation of eIF2 alpha. These results suggest that the immunosuppressive activity of BraA is induced by amino acid deprivation via the inhibition of system L and that the amino acid transporter is a target for immunosuppressant.
机译:T细胞活化中的淋巴细胞需要细胞外营养来为细胞增殖和效应功能提供能量。因此,营养转运蛋白的抑制剂有望成为一类新的免疫抑制剂。在这里,我们报告说,一种免疫抑制化合物Brasilicardin A(BraA)的分子靶标是氨基酸转运系统L。BraA抑制了鼠T细胞淋巴细胞CTLL-2细胞在G1期的细胞周期进程,并有效地抑制了该过程。氨基酸是氨基酸转运系统L的底物。此外,BraA刺激了GCN2激活,随后刺激了eIF2α的磷酸化。这些结果表明,通过抑制系统L,氨基酸剥夺诱导了BraA的免疫抑制活性,并且氨基酸转运蛋白是免疫抑制剂的靶标。

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