p38丝裂原活化蛋白激酶对HBZY-1系膜细胞株表达NF-κB和MCP-1的调控  

A role of p38 mitogen-activated protein kinase in regulation of NF-κB and MCP-1 expressions in HBZY-1 mesangial cell line

作　　者：魏倩萍[1] 邓华聪[1] 赵劼[2] 

机构地区：[1]重庆医科大学附属第一医院内分泌科,400016 [2]重庆医科大学超声工程研究所

出　　处：《中华内分泌代谢杂志》2008年第3期308-311,共4页Chinese Journal of Endocrinology and Metabolism

基　　金：国家自然科学基金资助项目（30570744）

摘　　要：目的探讨p38丝裂原活化蛋白激酶（p38 mitogen—activated protein kinase，p38MAPK）与NF—κB、单核细胞趋化蛋白1（monocyte chemoattractant protein-1，MCP-1）之间的关系，从而研究p38MAPK和NF—κB、MCP-1在糖尿病肾病中的作用机制。方法分别以高葡萄糖、高胰岛素、H2O2和糖基化终产物孵育大鼠肾小球系膜细胞株HBZY-1；先以p38MAPK特异抑制剂SB203580预处理细胞株HBZY-1，再给予上述4种因素孵育细胞株HBZY-1，观察其p38MAPK和NF—κB、MCP-1的表达。结果高葡萄糖、高胰岛素、H2O2和糖基化终产物均可独立激活p38MAPK，使其磷酸化表达量增加，NF—κB、MCP-1表达也明显增加；SB203580预处理后，NF—κB、MCP-1表达被显著抑制。结论p38MAPK可能通过激活NF—κB、MCP-1而诱导糖尿病时肾脏的损害，p38MAPK和NF—κB、MCP-1在糖尿病肾病的发生发展过程中可能起重要作用。Objective To investigate the relationship among p38 mitogen-activated protein kinase （p38MAPK） , NF-KB and monocyte chemoattractant protein-1 （MCP-1） , and to study the role of p38MAPK, NF- κB and MCP-1 in diabetic nephropathy. Methods Protein expressions of p38MAPK and NF-κB, and mRNA expression of MCP-1 were initially investigated in rat mesangial cell line HBZY-1, which were incubated separately with 25 mmol/L glucose, 100 nmol/L insulin, 100 μmol/L H2O2 and 100 mg/L advanced glycosylation end products（AGEs）. The relationship among p38MAPK, NF-κB and MCP-1 expression was observed by using SB203580, a specific inhibitor of p38MAPK. Results The expressions of p38MAPK, NF-κB and MCP-1 were increased in HBZY-1 cells incubated separately with 25 mmol/L glucose, 100 nmol/L insulin, 100 μmol/L H2O2 and 100 mg/L AGEs. Expressions of NF-κB and MCP-1 were significantly reduced when p38MAPK was inhibited by SB203580. Conclusion p38MAPK, NF-κB and MCP-1 are involved in development of diabetic nephropathy, and p38MAPK stimulation is essential for the expressions of NF-κB and MCP-1.

关 键 词：P38丝裂原活化蛋白激酶 NF—κB 单核细胞趋化蛋白1 糖尿病肾病 大鼠肾小球系膜细胞株HBZY-1 

分 类 号：R587.2[医药卫生—内分泌]