Suppr超能文献

血管活性肽对培养的系膜细胞胞质钙的影响。

Effects of vasoactive peptides on cytosolic calcium in cultured mesangial cells.

作者信息

Hassid A, Pidikiti N, Gamero D

出版信息

Am J Physiol. 1986 Dec;251(6 Pt 2):F1018-28. doi: 10.1152/ajprenal.1986.251.6.F1018.

Abstract

We have used the "second generation" Ca indicator, fura-2, to measure cytosolic free Ca concentrations in superfused cultures of adherent primary renal mesangial cells. The basal cytosolic free Ca concentration in these cells was found to be 93 +/- 5 nM (n = 35). The Ca ionophore ionomycin (0.1 microM) increased cytosolic Ca levels to a peak value of fourfold above basal, followed by a decline to a steadily maintained concentration of twofold above basal. Two vasoactive peptide hormones, arginine vasopressin and angiotensin II, at maximally effective concentrations, transiently increased cytosolic free Ca levels to peak values of three- and sixfold, respectively, above basal levels. The angiotensin II-evoked increase declined to near basal values before rising again to a value of 1.5- to 2-fold above basal. Cells treated with vasopressin did not have a significant secondary increase of Ca above a small, time-dependent, spontaneous increase. Mesangial cells demonstrated tachyphylaxis to both peptides. However, cross-tachyphylaxis was not observed. Treatment of cells with angiotensin II in ethyleneglycol-bis-(beta-aminoethylether)-N,N'-tetraacetic acid-supplemented Ca-deficient medium, or with the Ca channel blockers nifedipine or verapamil, did not eliminate the transient phase of cytosolic Ca metabolism. In contrast, the Ca channel blockers completely inhibited the second sustained Ca response to angiotensin II. These results indicate that angiotensin II and vasopressin mobilize intracellular Ca in cultured adherent mesangial cells. Angiotensin II, but not vasopressin, also appears to increase cytosolic Ca by influx of extracellular Ca through specific channels.

摘要

我们使用了“第二代”钙指示剂氟罗-2,来测量贴壁生长的原代肾系膜细胞灌流培养物中的胞质游离钙浓度。发现这些细胞中的基础胞质游离钙浓度为93±5 nM(n = 35)。钙离子载体离子霉素(0.1 μM)使胞质钙水平升高至基础值的四倍峰值,随后下降至稳定维持在基础值两倍的浓度。两种血管活性肽激素,精氨酸加压素和血管紧张素II,在最大有效浓度下,可使胞质游离钙水平分别短暂升高至基础水平之上三倍和六倍的峰值。血管紧张素II引起的升高在再次升至基础值之上1.5至2倍的值之前降至接近基础值。用加压素处理的细胞除了有一个小的、时间依赖性的自发升高外,没有明显的钙继发性升高。系膜细胞对这两种肽均表现出快速耐受性。然而,未观察到交叉快速耐受性。在补充乙二醇双(β-氨基乙基醚)-N,N'-四乙酸的缺钙培养基中用血管紧张素II处理细胞,或用钙通道阻滞剂硝苯地平或维拉帕米处理细胞,并未消除胞质钙代谢的瞬态阶段。相反,钙通道阻滞剂完全抑制了对血管紧张素II的第二次持续钙反应。这些结果表明,血管紧张素II和加压素可动员培养的贴壁系膜细胞内的钙。血管紧张素II似乎还通过特定通道使细胞外钙内流来增加胞质钙,而加压素则不然。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验