氧化性低密度脂蛋白oxLDL通过下调TET2诱导滋养细胞HTR-8/Svneo焦亡

Ting TAO , Jing YAN , Ziling LIAO , Wenmao ZHANG , Changqiong XU , Ran LI
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引用次数: 0

摘要

目的探讨TET2对氧化低密度脂蛋白(oxLDL)滋养细胞HTR-8/Svneo的热凋亡作用。方法用载药(0 mg/L)和oxLDL (50 mg/L)处理shtr -8/Svneo细胞24 h, Western blot检测oxLDL对HTR-8/Svneo细胞TET2表达的影响。在HTR-8/Svneo细胞中使用si-TET2进行TET2的敲除。CCK8、Transwell和创面愈合实验分别检测TET2敲低对HTR-8/Svneo细胞增殖、细胞周期、迁移和侵袭的影响。Western blot法定量si-TET2处理细胞中焦亡蛋白GSDMD和caspase-1的表达水平。结果soxldl呈浓度依赖性下调TET2表达。TET2敲低抑制HTR-8/Svneo侵袭和迁移,但促进细胞增殖。Western blot结果显示,TET2敲低可上调GSDMD和caspase-1的表达。结论oxldl通过下调TET2表达诱导HTR-8/Svneo细胞焦亡,减少滋养细胞侵袭和迁移。这些数据表明,tet2诱导的焦亡在妊娠病理中起关键作用,如先兆子痫。进一步的研究可以阐明这一过程的机制,并阐明潜在的预防和治疗靶点。
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Oxidative low-density lipoprotein oxLDL induces pyroptosis in trophoblast cells HTR-8/Svneo by downregulating TET2

Objective

To investigate pyroptosis in the trophoblast cells HTR-8/Svneo induced by TET2 in oxidized low-density lipoprotein (oxLDL).

Methods

HTR-8/Svneo cells were treated with vehicle (0 mg/L) and 50 mg/L oxLDL for 24 h. The effects of oxLDL on TET2 expression in HTR-8/Svneo cells were detected by Western blot. Knockdown of TET2 was performed in HTR-8/Svneo cells using si-TET2. CCK8, Transwell, and wound healing assays were used to detect the effect of TET2 knockdown on the proliferation, cell cycle, migration, and invasion of HTR-8/Svneo cells, respectively. Western blot was used to quantify the expression levels of the pyroptosis proteins GSDMD and caspase-1 in si-TET2 treated cells.

Results

oxLDL downregulates TET2 expression in a concentration-dependent manner. TET2 knockdown inhibits HTR-8/Svneo invasion and migration but promotes cell proliferation. Western blot results showed that TET2 knockdown upgregulated the expression of GSDMD and caspase-1.

Conclusion

oxLDL induces pyroptosis of HTR-8/Svneo by downregulating TET2 expression, resulting in decreased trophoblast invasion and migration. These data suggest that TET2-induced pyroptosis play a critical role in gestational pathologies, such as preeclampsia. Further studies can clarify the mechanisms of this process and elucidate potential preventive and therapeutic targets.

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