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乳酸通过依赖磷酸二酯酶-5 的途径抑制 iNKT 细胞的功能。

Lactic acid inhibits iNKT cell functions via a phosphodiesterase-5 dependent pathway.

机构信息

Division of Molecular Medicine, Hefei National Laboratory for Physical Sciences at Microscale, The CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Life Sciences, University of Science and Technology of China, China.

Division of Molecular Medicine, Hefei National Laboratory for Physical Sciences at Microscale, The CAS Key Laboratory of Innate Immunity and Chronic Disease, School of Life Sciences, University of Science and Technology of China, China.

出版信息

Biochem Biophys Res Commun. 2021 Apr 2;547:9-14. doi: 10.1016/j.bbrc.2021.02.012. Epub 2021 Feb 12.

Abstract

Lactic acid in tumor microenvironment inhibits iNKT cell functions and thus dampens their anti-tumor efficacy. The underlying mechanisms remain unclear. Here, we show that phosphodiesterase-5 inhibitors, sildenafil and tadalafil, promote IFN-γ and IL-4 production in iNKT cells in a cGMP-PKG pathway dependent manner. To favor their cytokine production, iNKT cells reduce Pde5a mRNA lever after activation. In line with the reduction of cytokines caused by lactic acid, lactic acid elevates Pde5a mRNA lever in activated iNKT cells. As a result, phosphodiesterase-5 inhibitor partially restores the cytokine production in lactic acid-treated cells. Our results demonstrate that phosphodiesterase-5 inhibits cytokine production in iNKT cells, and that contributes to the lactic acid-caused dysfunction of iNKT cells.

摘要

肿瘤微环境中的乳酸抑制 iNKT 细胞的功能,从而降低其抗肿瘤功效。其潜在机制尚不清楚。在这里,我们表明磷酸二酯酶-5 抑制剂西地那非和他达拉非通过 cGMP-PKG 途径依赖性促进 iNKT 细胞中 IFN-γ 和 IL-4 的产生。为了促进细胞因子的产生,iNKT 细胞在激活后降低 Pde5a mRNA 水平。与乳酸引起的细胞因子减少一致,乳酸在激活的 iNKT 细胞中升高 Pde5a mRNA 水平。结果,磷酸二酯酶-5 抑制剂部分恢复了乳酸处理细胞中的细胞因子产生。我们的结果表明,磷酸二酯酶-5 抑制 iNKT 细胞中的细胞因子产生,这有助于乳酸引起的 iNKT 细胞功能障碍。

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