Kuo Hung-Tien, Shin Shyi-Jang, Kuo Mei-Chuan, Chen Hung-Chun
Division of Nephrology, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.
Kaohsiung J Med Sci. 2006 Aug;22(8):371-6. doi: 10.1016/S1607-551X(09)70325-0.
Angiotensin II (Ang-II) is a potent vasoactive hormone, which plays an important role in the pathogenesis of glomerulosclerosis. Ang-II activates many cytokine systems in the kidney. Recent studies indicate that Ang-II is closely related to the activation of the endothelin-1 (ET-1) system. The present study was designed to measure the [H3]-thymidine uptake and fibronectin production of cultured rat mesangial cells stimulated with Ang-II, and to evaluate the effects of specific ET-1 receptor antagonists, BQ123 (type A receptor antagonist) and IRL1038 (type B receptor antagonist) on the cells. ET-1 was measured by radioimmunoassay and fibronectin by Western blot analysis. The results were as follows: (1) Ang-II enhanced ET-1 production, [H3]-thymidine uptake, number of cells, and fibronectin production of mesangial cells; (2) all the baseline [H3]-thymidine uptake, number of cells, and fibronectin production of mesangial cells can be partly suppressed by BQ123, but not by IRL1038; (3) the increment of Ang-II-enhanced number of cells can be partly suppressed by BQ123, but not by IRL1038; and (4) the increment of Ang-II-enhanced fibronectin production can be partly suppressed by both BQ123 and IRL1038. Our results indicate that Ang-II is an active stimulant for the proliferation and fibronectin production of mesangial cells, and the effect is partly suppressed mainly by ET-1 type A receptor antagonists.
血管紧张素II(Ang-II)是一种强效血管活性激素,在肾小球硬化的发病机制中起重要作用。Ang-II激活肾脏中的许多细胞因子系统。最近的研究表明,Ang-II与内皮素-1(ET-1)系统的激活密切相关。本研究旨在测量用Ang-II刺激的培养大鼠系膜细胞的[H3]-胸腺嘧啶核苷摄取和纤连蛋白生成,并评估特异性ET-1受体拮抗剂BQ123(A型受体拮抗剂)和IRL1038(B型受体拮抗剂)对细胞的影响。通过放射免疫测定法测量ET-1,通过蛋白质印迹分析测量纤连蛋白。结果如下:(1)Ang-II增强系膜细胞的ET-1生成、[H3]-胸腺嘧啶核苷摄取、细胞数量和纤连蛋白生成;(2)系膜细胞的所有基线[H3]-胸腺嘧啶核苷摄取、细胞数量和纤连蛋白生成可被BQ123部分抑制,但不能被IRL1038抑制;(3)Ang-II增强的细胞数量增加可被BQ123部分抑制,但不能被IRL1038抑制;(4)Ang-II增强的纤连蛋白生成增加可被BQ123和IRL1038两者部分抑制。我们的结果表明,Ang-II是系膜细胞增殖和纤连蛋白生成的活性刺激物,并且该作用主要被ET-1A型受体拮抗剂部分抑制。