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首页|期刊导航|中国病理生理杂志|Men1通过调控FTO/ALKBH5表达和减少m6A甲基化而抑制小鼠肾纤维化

Men1通过调控FTO/ALKBH5表达和减少m6A甲基化而抑制小鼠肾纤维化

杨云巧 陈腾祥 金帮明 田倩婷 潘婷 朱佳美 王子名 王旭艳 张拓 周宇霞 郭兵

中国病理生理杂志2024,Vol.40Issue(12):2193-2201,9.
中国病理生理杂志2024,Vol.40Issue(12):2193-2201,9.DOI:10.3969/j.issn.1000-4718.2024.12.001

Men1通过调控FTO/ALKBH5表达和减少m6A甲基化而抑制小鼠肾纤维化

Men1 inhibits mouse renal fibrosis by regulating FTO/ALKBH5 expres-sion and reducing m6A methylation

杨云巧 1陈腾祥 2金帮明 2田倩婷 3潘婷 1朱佳美 1王子名 1王旭艳 1张拓 4周宇霞 4郭兵4

作者信息

  • 1. 贵州医科大学基础医学院生理教研室,贵州 贵阳 561113||贵州医科大学慢性病诊疗转化工程研究中心,贵州 贵阳 561113
  • 2. 贵州医科大学基础医学院生理教研室,贵州 贵阳 561113||贵州医科大学慢性病诊疗转化工程研究中心,贵州 贵阳 561113||贵州医科大学附属医院贵州精准医学研究院,贵州 贵阳 550003||贵州医科大学贵州省常见病发病机制与药物研究重点实验室,贵州 贵阳 561113
  • 3. 贵州医科大学基础医学院生理教研室,贵州 贵阳 561113||贵州医科大学慢性病诊疗转化工程研究中心,贵州 贵阳 561113||贵州医科大学附属医院贵州精准医学研究院,贵州 贵阳 550003
  • 4. 贵州医科大学基础医学院生理教研室,贵州 贵阳 561113||贵州医科大学慢性病诊疗转化工程研究中心,贵州 贵阳 561113||贵州医科大学贵州省常见病发病机制与药物研究重点实验室,贵州 贵阳 561113
  • 折叠

摘要

Abstract

AIM:To explore the role and molecular mechanism of Men1 gene in regulating mouse renal fibro-sis.METHODS:A unilateral ureteral obstruction(UUO)-induced renal fibrosis model was established using C57BL/6 mice,and the mice were randomly divided into 4 groups:sham,UUO-3 d,UUO-7 d,and UUO-14 d,with 15 mice in each group.The C57BL/6 mice with Men1 knockout were randomly divided into 4 groups:sham-Men1-WT,sham-Men1-CKO,UUO-Men1-WT,and UUO-Men1-CKO,with 8 mice in each group.HE staining,Masson staining,and Sirius red staining were used to detect UUO-induced renal injury and renal fibrosis.Human renal tubular epithelial HK-2 cells with MEN1 knockout were constructed.RT-qPCR,Western blot,immunohistochemistry and immunoflurorescnence were per-formed to detect the mRNA and protein expression of MEN1,fibrosis markers(α-smooth muscle actin,collagen type Ⅲ and fibronectin 1)and m6A-related proteins[methyltransferase-like 3(METTL3),METTL14,YTH domain family pro-tein 2(YTHDF2),AlkB homolog 5(ALKBH5),and fat mass and obesity-associated protein(FTO)]in UUO mouse kid-ney tissues and transforming growth factor-β(TGF-β;10 µg/L)-treated HK-2 cells.Dot blot analysis was conducted to measure m6A methylation levels in both mouse kidney tissuess and HK-2 cells.RESULTS:The expression of Men1 de-creased with the aggravation of renal fibrosis(P<0.01).Men1 inhibited the expression of fibrosis markers in renal tis-sues,and MEN1 knockout increased the accumulation of collagen induced by UUO and TGF-β(P<0.01).The expres-sion of FTO and ALKBH5 in mouse kidney tissues and HK-2 cells was down-regulated by MEN1 knockout(P<0.01),and the methylation level of m6A was increased(P<0.01).Overexpression of FTO significantly reduced the accumulation of m6A modifications and renal fibrosis caused by MEN1 loss,and the methylation level of m6A was increased(P<0.01).CONCLUSION:Loss of Men1 gene promotes renal fibrosis in mice,and Men1 suppresses renal fibrosis in mice by pro-moting the expression of FTO/ALKBH5 to reduce m6A modifications.

关键词

Men1基因/肾纤维化/单侧输尿管结扎/m6A RNA甲基化/FTO/ALKBH5

Key words

Men1 gene/renal fibrosis/unilateral ureteral obstruction/m6A RNA methylation

分类

医药卫生

引用本文复制引用

杨云巧,陈腾祥,金帮明,田倩婷,潘婷,朱佳美,王子名,王旭艳,张拓,周宇霞,郭兵..Men1通过调控FTO/ALKBH5表达和减少m6A甲基化而抑制小鼠肾纤维化[J].中国病理生理杂志,2024,40(12):2193-2201,9.

基金项目

国家自然科学基金资助项目(No.32160144) (No.32160144)

中国博士后科学基金资助项目(No.2023MD734162) (No.2023MD734162)

贵州省卫生健康委科学技术基金项目(No.gzwkj2022-231) (No.gzwkj2022-231)

中国病理生理杂志

OA北大核心CSTPCD

1000-4718

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