miR-148a-5p参与了高蛋氨酸饮食诱导ApoE^-/-小鼠的肝细胞凋亡  被引量:6

Involvement of miR-148a-5p in ApoE^-/-mouse hepatocyte apoptosis induced by high methionine diet

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作  者:马芳 张辉[2] 李桂忠[2,3,4] 马胜超 沈江涌[2,5] 孙磊 郝银菊 马生贤[2] 姜怡邓 Ma Fang;Zhang Hui;Li Guizhong;Ma Shengchao;Shen Jiangyong;Sun Lei;Hao Yinju;Ma Shengxian;Jiang Yideng(School of Clinical Medicine,Yinchuan 750004,Ningxia Hui Autonomous Region,China;School of Clinical Medicine,School of Basic Medicine,Yinchuan 750004,Ningxia Hui Autonomous Region,China;State Key Laboratory of Metabolic Cardiovascular Disease,National Health Commission of China,Yinchuan 750004,Ningxia Hui Autonomous Region,China;Ningxia Key Laboratory of Vascular Injury and Repair,Yinchuan 750004,Ningxia Hui Autonomous Region,China;Department of Plastic Surgery,General Hospital of Ningxia Medical University,Yinchuan 750004,Ningxia Hui Autonomous Region,China;School of Clinical Medicine,School of Pharmacy,Ningxia Medical University,Yinchuan 750004,Ningxia Hui Autonomous Region,China)

机构地区:[1]宁夏医科大学临床医学院,宁夏回族自治区银川市750004 [2]宁夏医科大学基础医学院,宁夏回族自治区银川市750004 [3]国家卫生健康委代谢性心血管疾病研究重点实验室,宁夏回族自治区银川市750004 [4]宁夏血管损伤与修复研究重点实验室,宁夏回族自治区银川市750004 [5]宁夏医科大学总医院烧伤整形外科,宁夏回族自治区银川市750004 [6]宁夏医科大学药学院,宁夏回族自治区银川市750004

出  处:《中国组织工程研究》2020年第35期5632-5637,共6页Chinese Journal of Tissue Engineering Research

基  金:国家自然科学基金(81670416),项目负责人:姜怡邓;国家自然科学基金(81660088),项目参与人:张辉;宁夏自然科学基金(2018AAC03265),项目负责人:郝银菊;宁夏医科大学2018年“大学生创新创业计划项目”(201810751007),项目负责人:马生贤。

摘  要:背景:高蛋氨酸饮食可以导致ApoE^-/-小鼠发生肝损伤,微小RNA(miRNA)参与细胞存活、分化和细胞凋亡等各种细胞过程,具有重要意义。目的:探讨miR-148a-5p在高蛋氨酸饮食诱导ApoE^-/-小鼠肝细胞凋亡中的作用。方法:12只ApoE^-/-小鼠随机分为2组,每组6只,ApoE^-/-对照组为普通饮食,ApoE^-/-高蛋氨酸组为高蛋氨酸饮食。苏木精-伊红染色观察2组肝组织形态学变化;TUNEL染色观察肝细胞的凋亡情况;Western blot测定Bax、Bcl-2的表达改变;荧光定量PCR检测miR-148a-5p的表达;运用Target Scan靶基因预测软件预测miR-148a-5p的靶基因;双荧光素酶活性实验明确其靶向关系。结果与结论:①与对照组相比,ApoE^-/-高蛋氨酸组肝脏组织肝小叶结构发生明显紊乱,部分细胞呈胞浆疏松化变性,肝细胞凋亡增加,Bax的表达明显上升且Bcl-2的表达显著下降(P<0.01);②荧光定量PCR结果显示,ApoE^-/-高蛋氨酸组miR-148a-5p的表达增加(P<0.05);③靶基因预测软件提示,Bcl-2为miR-148a-5p的潜在靶基因;④双荧光素酶活性实验确定了miR-148a-5p与Bcl-2的靶向关系(P<0.05);⑤肝细胞中过表达miR-148a-5p后Bax的表达显著上升且Bcl-2的表达明显下降(P<0.01);⑥提示在高蛋氨酸饮食诱导的ApoE^-/-小鼠肝细胞中,miR-148a-5p通过负调控Bcl-2促进肝细胞凋亡,这可能是造成肝损伤的机制之一。BACKGROUND:High methionine diet can cause liver damage in ApoE^-/-mice,and microRNAs(miRNAs)are involved in various cell processes such as cell survival,differentiation,and apoptosis,which is of great significance.OBJECTIVE:To investigate the effect of miR-148a-5p on ApoE^-/-mouse hepatocyte apoptosis induced by high methionine diet.METHODS:Twelve ApoE^-/-mice aged 5 weeks were randomly divided into two groups with six ApoE^-/-mice in each group:ApoE^-/-control group was fed with a normal diet,and ApoE^-/-high methionine diet group(ApoE^-/-+HMD)was fed with a high methionine diet.Hematoxylin-eosin staining was used to observe the morphological changes of liver tissues in the two groups.TUNEL staining was used to observe the apoptosis of hepatocytes.The expressions of Bax and Bcl-2 were detected by western blot.Fluorescence quantitative PCR was used to detect the expression of miR-148a-5p.Target Scan prediction software was used to predict the target gene of miR-148a-5p,and double luciferase activity assay was used to verify the targeted relationship.RESULTS AND CONCLUSION:Compared with the control group,the hepatic lobular structure of the ApoE^-/-mice with high methionine diet was obviously disturbed,and some cells showed cytoplasmic osteoporosis;hepatocyte apoptosis increased;the expression of Bax significantly increased and the expression of Bcl-2 significantly decreased(P<0.01).Fluorescence quantitative PCR results showed that the expression of miR-148a-5p increased in the ApoE^-/-mice with high methionine diet(P<0.05).The target gene prediction software indicated that Bcl-2 was a potential target gene of miR-148a-5p,and the targeted relationship between miR-148a-5p and Bcl-2 was confirmed by the double luciferase activity assay(P<0.05).After miR-148a-5p was overexpressed in hepatocytes,Bax expression increased and Bcl-2 expression decreased significantly(P<0.01).In conclusion,miR-148a-5p promoted hepatocyte apoptosis through negative regulation of Bcl-2 in ApoE^-/-mouse hepatocytes induced by high methionine

关 键 词:miR-148a-5p BCL-2 高蛋氨酸饮食 肝细胞 凋亡 动物 

分 类 号:R459.9[医药卫生—治疗学] R318[医药卫生—临床医学]

 

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