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ASIC1a inhibits cell pyroptosis induced by acid‐induced activation of rat hepatic stellate cells

机译:ASIC1A抑制酸诱导的大鼠肝星状细胞的激活诱导的细胞糊化症

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The activation of hepatic stellate cells (HSCs) is associated with liver fibrosis, the pathological feature of most forms of chronic hepatic damage, and is accompanied by abnormal deposition of the extracellular matrix (ECM). During the pathological process, acid‐sensing ion channel 1a (ASIC1a), which is responsible for Casup2+/sup transportation, is involved in the activation of HSCs. It has previously been identified that ASIC1a is related to pyroptosis in articular chondrocytes. However, it remains unclear whether ASIC1a restrains pyroptosis during liver fibrosis. Here, we determined that the levels of pyroptosis‐associated speck‐like protein, gasdermin D, caspase‐1, nucleotide‐binding oligomerization domain (NOD)‐like receptor 3, and apoptosis‐associated speck‐like protein (ASC) decreased, while the level of α‐smooth muscle actin and collagen‐I increased upon introduction of ASIC1a into an acid‐induced model. Inhibition or silencing of ASIC1a and the use of Casup2+/sup‐free medium were able to promote the pyroptosis of activated HSCs, which reduced their deposition. In summary, our study indicates that ASIC1a inhibits pyroptosis of HSCs and that inhibition of ASIC1a may be able to promote pyroptosis to relieve liver fibrosis.
机译:肝星状细胞(HSCs)的激活与肝纤维化有关,大多数形式的慢性肝损伤的病理特征,并且伴随细胞外基质(ECM)的异常沉积。在病理过程中,酸感测离子通道1a(ASIC1a),其负责Ca 2 + / sup>运输,参与HSC的活化。先前已识别出ASIC1A与关节软骨细胞的糊菌有关。然而,它仍然尚不清楚ASIC1A在肝纤维化期间是否抑制糊虫病。在这里,我们确定釜凋亡相关的斑点蛋白质,燃料蛋白D,caspase-1,核苷酸结合寡聚化结构域(NOD)的水平,核苷酸结合的寡聚域(NOD),以及凋亡相关的斑点蛋白(ASC)减少在将ASIC1a引入酸性诱导的模型时,α-平滑肌肌动蛋白和胶原蛋白-1的水平增加。 ASIC1a的抑制或沉默和使用Ca 2 + -free培养基能够促进活化HSC的糊死,这降低了它们的沉积。总之,我们的研究表明ASIC1A抑制HSC的糊化酶,并且ASIC1A的抑制可能能够促进糊化症以缓解肝纤维化。

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