SIRT2
下调和上调
组蛋白脱乙酰基酶
锡尔图因
细胞生物学
西妥因1
活力测定
滋养层
生物
癌症研究
组蛋白
基因敲除
小RNA
组蛋白脱乙酰酶抑制剂
表观遗传学
曲古抑菌素A
化学
HDAC6型
基因沉默
HDAC1型
乙酰化
分子生物学
细胞凋亡
胎盘
基因
生物化学
胎儿
怀孕
遗传学
作者
Yi‐Kuo Yu,Xiaoqin An,Daiming Fan
标识
DOI:10.1007/s43032-020-00398-x
摘要
Reduced activity of trophoblast cells is well-recognized to lead to preeclampsia (PE) progression. This study aims to evaluate the roles of histone deacetylase sirtuin 2 (SIRT2) in activity of trophoblast cells and the molecules involved. Differentially expressed genes in placental tissues between PE patients and healthy individuals were screened using microarray analyses. SIRT2 and atypical chemokine receptor 2 (ACKR2) were downregulated while miR-146a was upregulated in PE patients. SIRT2 was localized in placental syncytiotrophoblasts. Upregulation of SIRT2 enhanced viability, migration and invasion, while reduced apoptosis of HTR-8/SVneo cells. SIRT2 was found to trigger p65 deacetylation level and suppress miR-146a expression according to the luciferase and ChIP assays, whereas miR-146a was found to target ACKR2. Downregulation of p65 promoted migration and invasion of cells. Overexpression of miR-146a inhibited cell viability and blocked the function of SIRT2. ACKR2 was downregulated in tissues from PE women and its upregulation blocked the role of miR-146a. To conclude, SIRT2 promotes p65 deacetylation to suppress miR-146a expression and upregulates ACKR2 expression, therefore enhancing proliferation, migration, and invasion of HTR-8/SVneo cells. This study may offer novel thoughts into the management of PE.
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