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半胱氨酸天冬氨酸蛋白酶-2 介导甘油三酯(TG)诱导的巨噬细胞死亡。

Caspase-2 mediates triglyceride (TG)-induced macrophage cell death.

机构信息

Department of Biomedical Laboratory Science, College of Health Sciences, Yonsei University, Wonju 26493; Department of Clinical Laboratory Science, College of Medical Sciences, Daegu Haany University, Gyeongsan 38610, Korea.

Department of Biomedical Laboratory Science, College of Health Sciences, Yonsei University, Wonju 26493, Korea; Department of Biomedical Laboratory Science, College of Natural Science, Gimcheon University, Gimcheon 39528, Korea.

出版信息

BMB Rep. 2017 Oct;50(10):510-515. doi: 10.5483/bmbrep.2017.50.10.106.

Abstract

Triglyceride (TG) accumulation causes macrophage cell death, which affects the development of atherosclerosis. Here, we examined whether caspase-2 is implicated in TG-induced macrophage cell death. We found that caspase-2 activity is increased in TG-treated THP-1 macrophages, and that inhibition of caspase-2 activity drastically inhibits TG-induced cell death. We previously reported that TG-induced macrophage cell death is triggered by caspase-1, and thus investigated the relationship between caspase-2 and caspase-1 in TG-induced macrophage cell death. Inhibition of caspase-2 activity decreased caspase-1 activity in TG-treated macrophages. However, caspase-1 inhibition did not affect caspase-2 activity, suggesting that caspase-2 is upstream of caspase-1. Furthermore, we found that TG induces activation of caspase-3, -7, -8, and -9, as well as cleavage of PARP. Inhibition of caspase-2 and -1 decreased TG-induced caspase-3, -7, -8, and -9 activation and PARP cleavage. Taken together, these results suggest that TG-induced macrophage cell death is mediated via the caspase-2/caspase-1/apoptotic caspases/PARP pathways. [BMB Reports 2017; 50(10): 510-515].

摘要

甘油三酯 (TG) 积累会导致巨噬细胞死亡,从而影响动脉粥样硬化的发展。在这里,我们研究了半胱氨酸蛋白酶-2 是否参与了 TG 诱导的巨噬细胞死亡。我们发现,TG 处理的 THP-1 巨噬细胞中半胱氨酸蛋白酶-2 活性增加,而半胱氨酸蛋白酶-2 活性的抑制则显著抑制 TG 诱导的细胞死亡。我们之前报道过 TG 诱导的巨噬细胞死亡是由半胱氨酸蛋白酶-1 触发的,因此我们研究了半胱氨酸蛋白酶-2 和半胱氨酸蛋白酶-1 在 TG 诱导的巨噬细胞死亡中的关系。半胱氨酸蛋白酶-2 活性的抑制降低了 TG 处理的巨噬细胞中的半胱氨酸蛋白酶-1 活性。然而,半胱氨酸蛋白酶-1 的抑制并不影响半胱氨酸蛋白酶-2 活性,这表明半胱氨酸蛋白酶-2 位于半胱氨酸蛋白酶-1 的上游。此外,我们发现 TG 诱导了半胱氨酸蛋白酶-3、-7、-8 和 -9 的激活以及 PARP 的切割。半胱氨酸蛋白酶-2 和 -1 的抑制降低了 TG 诱导的半胱氨酸蛋白酶-3、-7、-8 和 -9 的激活以及 PARP 的切割。综上所述,这些结果表明,TG 诱导的巨噬细胞死亡是通过半胱氨酸蛋白酶-2/半胱氨酸蛋白酶-1/凋亡半胱氨酸蛋白酶/PARP 途径介导的。[BMB 报告 2017; 50(10): 510-515]。

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