论著(基础研究)

蛋白激酶MPK-1通过DAF-16调控FAT-7抑制脂质累积

  • 韩三峰 ,
  • 黄黎莹 ,
  • 王立顺
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  • 上海交通大学 医学院附属瑞金医院分子医学中心,上海 200025
韩三峰(1986—),男,硕士; 电子信箱: lovey1123@yahoo.cn。

网络出版日期: 2013-08-22

Protein kinase MPK-1 inhibits fat accumulation via regulating FAT-7 by DAF-16

  • HAN San-feng ,
  • HUANG Li-ying ,
  • WANG Li-shun
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  • Center for Molecular Medicine, Ruijin Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China

Online published: 2013-08-22

摘要

目的 探讨蛋白激酶MPK-1对脂质代谢的影响及可能的作用机制。方法 用秀丽线虫(C.elegans)作为模式生物,采用RNA干扰(RNAi)技术定向干扰mpk-1,sbp-1、daf-2基因表达,油红O和苏丹黑染色观察线虫脂质含量的变化,洗脱脂肪进行定量分析确定脂肪含量的增减。采用RNAi技术结合对线虫体内特定位置绿色荧光蛋白表达变化的观察,分析MPK-1影响脂肪累积的可能机制。结果 干扰mpk-1基因表达后,线虫体内脂肪含量明显增加。荧光显微镜观察发现:脂质合成酶fat-7∷gfp线虫干扰mpk-1基因表达后,荧光增强;表达调控fat-7的转录因子DAF-16荧光蛋白的线虫品系中干扰mpk-1基因表达,可促进DAF-16向核内转移。结论 蛋白激酶MPK-1可能通过DAF-16调控FAT-7的活性,抑制脂肪的合成代谢,减少脂质累积。

本文引用格式

韩三峰 , 黄黎莹 , 王立顺 . 蛋白激酶MPK-1通过DAF-16调控FAT-7抑制脂质累积[J]. 上海交通大学学报(医学版), 2013 , 33(7) : 965 . DOI: 10.3969/j.issn.1674-8115.2013.07.014

Abstract

Objective To investigate the effect of protein kinase MPK-1 on lipid metabolism, and explore the underlying mechanism. Methods C.elegans was served as model organism, and the expression of mpk-1, sbp-1 and daf-2 genes was interfered with RNA interference (RNAi). The fat contents in C.elegans were observed by Oil-red O staining and Sudan black staining, and were quantified after washing off the dye. Then, the mechanism of effect of MPK-1 on fat accumulation was determined by the combination of RNAi knockdown technique and the green fluorescence change in a specified location. Results The fat content significantly increased after interference of mpk-1 gene expression. Fluorescence microscopy revealed that fluorescence enhancement was detected after interference of mpk-1 gene expression in C.elegans with expression of lipogenic enzymes fat-7∷gfp, and intranuclear transference of DAF-16 was promoted after interference of mpk-1 gene expression in C.elegans with expression of DAF-16 fluorescin regulating fat-7. Conclusion Protein kinase MPK-1 may inhibit FAT-7 activity through DAF-16, and reduce the fat accumulation.

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