同型半胱氨酸通过促进脂肪组织TRB3表达抑制PI3K/Akt信号通路

王雅楠; 李治纲; 张超; 李树德; 李涛; 彭建志

同型半胱氨酸通过促进脂肪组织TRB3表达抑制PI3K/Akt信号通路

1. 内蒙古医科大学附属医院病理科
2. 昆明医科大学生物化学与分子生物学系
3. 昆明学院医学院
4. 昆明医科大学第二附属医院营养科

基金项目:

基金：云南省科技厅-昆明医科大学应用基础研究联合专项基金资助项目 (2009CD213); 云南省教育厅科研基金资助项目 (2015Y398);

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出版历程
- 收稿日期: 2017-04-19

Homocysteine Suppress PI3K/Akt Signaling Pathway via Promoting the Expression of TRB3 in Adipose Tissue

Funds:

基金：云南省科技厅-昆明医科大学应用基础研究联合专项基金资助项目 (2009CD213); 云南省教育厅科研基金资助项目 (2015Y398);

摘要

摘要: 目的建立高同型半胱氨酸血症的动物模型, 检测脂肪组织TRB3的表达, 探讨TRB3对PI3K/Akt信号通路的影响.方法 20只昆明小鼠分为正常对照组和高同型半胱氨酸血症组, 每组10只.饮用含1.5%蛋氨酸3个月建立高同型半胱氨酸血症组模型.2组麻醉处死后取脂肪组织, 逆转录PCR检测TRB3、Akt和GLUT4的m RNA表达水平, Western blot检测TRB3、Akt、p-Akt (473) 和GLUT4的蛋白质表达水平.结果高同型半胱氨酸血症组的TRB3的m RNA表达较正常对照组增加 (P<0.05) , Akt和GLUT4的m RNA表达较正常对照组降低, 但差异无统计学意义 (P>0.05) ;高同型半胱氨酸血症组的TRB3的蛋白质表达较正常对照组增加 (P<0.05) , p-Akt (473) 蛋白质的表达降低, Akt和GLUT4的蛋白质表达差异无统计学意义 (P>0.05) .结论同型半胱氨酸可能通过增加脂肪组织TRB3的表达, 降低p-Akt (473) 和GLUT4蛋白质含量, 抑制PI3K/Akt信号通路, 影响脂肪组织对葡萄糖的摄取和利用.
- 高同型半胱氨酸血症 /
- TRB3 /
- PI3K/Akt信号通路 /
- GLUT4 /
- 脂肪组织
Abstract: Objective To build animal model of hyperhomocysteinemia (HHcy) , and to investigate the expression of TRB3 in adipose tissue and explore the effect of PI3K/Akt signaling pathway by TRB3.Me thods Twenty mice were divided into the fasting control group (n = 10) and the fasting HHcy group (n = 10) . Normal food was fed in the fasting control group. Normal food and 1.5% (mass fraction) methionine were fed in the fasting HHcy group.After the mice in every group were fed for three months.Adipose tissue in two groups was The m RNA expressions of TRB3, Akt and glucose transporter 4 (GLUT4) were detected by reverse transcription PCR.The protein expression of TRB3, Akt, p-Akt (473) and GLUT4 were measured by Western blot. Re s ults The m RNA expression of TRB3 in the fast HHcy group was increasedas compared with the control group. The m RNA expression of Akt and GLUT4 was decreased, however the result had no significant difference between two groups.Compared with the control group, the protein expression of TRB3 was increased and the protein expression of p-Akt (473) was reduced in the fast HHcy group. Whereas the protein expression of Akt and GLUT4 had no significant diffenence between two groups. Conclus ion Homocysteine may incease the uptake and utilization of glucose in adipose tissue by inhibiting PI3K/Akt signaling pathway, which may be the results of inducing the expression of TRB3 and downregulating the protein expression of p-Akt (473) and GLUT4.
- Hyperhomocysteinemia /
- TRB3 /
- Glucose transporter 4 /
- PI3K/Akt signaling pathway /
- Adipose tissue

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参考文献(11)

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