5-氮杂-2"-脱氧胞嘧啶核苷通过抑制大鼠原代肾肌成纤维细胞 Epo基因启动子高甲基化逆转PMT
作者:
作者单位:

天津市医药科学研究所

中图分类号:

R572

基金项目:

天津市卫生健康科技项目(No. TJWJ2022MS050)


5-aza-2 "-deoxycytosine reverses PMT by inhibiting Epo gene promoter hypermethylation in rat primary renal myoblasts______________________________________________________________
Author:
Affiliation:

1.Tianjin Institute of Medical &2.Pharmaceutical Sciences

Fund Project:

Tianjin Health Research Project (Grant No: TJWJ2022MS050)

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    摘要:

    目的 观察去甲基化剂5-氮杂-2′-脱氧胞苷(5-Aza-2"-deoxycytidine,5-Aza-CdR)对大鼠原代肾肌成纤维细胞的周细胞肌成纤维细胞转化(pericyte-myofibroblast transition,PMT)的影响。方法 5-Aza-CdR 250 ng/ml处理大鼠原代肾肌成纤维细胞72h,采用焦磷酸测序方法检测Epo启动子甲基化程度,采用免疫荧光与Western blot检测α-SMA、PDGFRβ和DNA甲基转移酶(DNMT3a)的蛋白表达水平,并检测细胞上清液EPO水平。结果 与对照组相比,5-Aza-CdR 处理能显著降低Dnmt3a的表达和EPO启动子高甲基化水平,并随之降低了肌成纤维细胞中α-SMA的表达及α-SMA与PDGFRβ的表达比例,同时,5-Aza-CdR 处理提高了细胞上清液中EPO的水平。结论 5-Aza-CdR可通过抑制大鼠原代肾肌成纤维细胞Epo启动子高甲基化逆转PMT。

    Abstract:

    Objective To observe the effect of demethylating agent 5-aza-2 "-deoxycytidine (5-Aza-CdR) on pericyte-myofibroblast transition(PMT)of primary rat renal myofibroblast. Methods Rat primary renal myofibroblast were treated with 5-Aza-CdR 250 ng/ml for 72h, and the methylation degree of Epo promoter was detected by pyrosequencing. The protein expression levels of α-SMA, PDGFRβ and DNA methyltransferase (DNMT3a) were detected by immunofluorescence and Western blot, and EPO levels in the supernatant were detected. Results Compared with control group, 5-Aza-CdR treatment significantly decreased the expression of Dnmt3a and the hypermethylation level of Epo promoter, and subsequently decreased the expression of α-SMA and the expression ratio of α-SMA to PDGFRβ in myofibroblast. Meanwhile, 5-Aza-CdR treatment increased the level of EPO in the cell supernatant. Conclusions 5-Aza-CdR can reverse PMT by inhibiting Epo promoter hypermethylation in primary renal myofibroblast.

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  • 收稿日期:2024-05-08
  • 最后修改日期:2024-09-10
  • 录用日期:2025-02-19
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