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首页> 外文期刊>Cell Reports >Glutathione Transferase Omega-1 Regulates NLRP3 Inflammasome Activation through NEK7 Deglutathionylation
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Glutathione Transferase Omega-1 Regulates NLRP3 Inflammasome Activation through NEK7 Deglutathionylation

机译:谷胱甘肽转移酶OMEGA-1通过NEK7脱藻硫化调节NLRP3炎症组活化

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The NLRP3 inflammasome is a cytosolic complex sensing phagocytosed material and various damage-associated molecular patterns, triggering production of the pro-inflammatory cytokines interleukin-1 beta (IL)-1β and IL-18 and promoting pyroptosis. Here, we characterize glutathione transferase omega 1-1 (GSTO1-1), a constitutive deglutathionylating enzyme, as a regulator of the NLRP3 inflammasome. Using a small molecule inhibitor of?GSTO1-1 termed C1-27, endogenous GSTO1-1 knockdown, and GSTO1-1sup?/?/sup mice, we report that GSTO1-1 is involved in NLRP3 inflammasome activation. Mechanistically, GSTO1-1 deglutathionylates cysteine 253 in NIMA related kinase 7 (NEK7) to promote NLRP3 activation. We therefore identify GSTO1-1 as an NLRP3 inflammasome regulator, which has potential as a drug target to limit NLRP3-mediated inflammation.
机译:NLRP3炎性组是一种细胞溶质复合物感测吞噬物质和各种损伤相关的分子模式,触发促炎细胞因子白细胞介素-1β(IL)-1β和IL-18的产生并促进糊酶。在此,我们表征谷胱甘肽转移酶Omega 1-1(GSTO1-1),构成脱氮硫化酶,作为NLRP3炎症的调节剂。使用αGsto1-1的小分子抑制剂被称为C1-27,内源性GSTO1-1敲低,GSTO1-1 α/α/α/ sup>小鼠,我们报告了GSTO1-1参与NLRP3炎症组活化。机械地,在NiMA相关激酶7(NEK7)中,GSTO1-1脱硫氨酸半胱氨酸253,以促进NLRP3活化。因此,我们鉴定了GSTO1-1作为NLRP3炎性调节剂,其具有限制NLRP3介导的炎症的药物靶标。

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