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[3H]哇巴因与培养的内皮细胞的结合:胆固醇富集的影响。

[3H]ouabain binding to cultured endothelial cells: effect of cholesterol enrichment.

作者信息

Lau Y T, Chen J K, Hsu M M, Yu H M

机构信息

Department of Physiology, Chang Gung Medical College, Kweisan, Taiwan, ROC.

出版信息

Life Sci. 1994;54(6):393-9. doi: 10.1016/0024-3205(94)00697-0.

Abstract

Binding experiments were performed with [3H]ouabain on cultured human umbilical vein endothelial cells (huvEC). Saturation studies yielded a binding capacity (Bmax) of 820 +/- 81 fmole/mg pr.(n = 4) and dissociation constant (KD) of 11.7 +/- 2.1nM (n = 4) in K(+)-free buffer for specific [3H] ouabain binding on these cells. External K+ inhibited this binding in a dose-dependent manner. The mean value of Bmax is equivalent to about 4 x 10(5) sites per cell, comparable with that of smooth muscle cell. These data demonstrated the presence of specific [3H]ouabain binding linked to Na+/K+ pump, consistent with the observations of ouabain-sensitive 86Rb uptake in huvEC. Effect of cholesterol enrichment was also studied. Incubation in media supplemented with cholesterol-phospholipid liposomes of molar ratio of 2:1 for 18 hours reduced the Bmax by 31% (P < 0.05) without significantly changed the value of KD. This reduction of [3H]ouabain binding appeared to be specific for cholesterol since liposome made with pure phospholipid did not alter binding. Recent findings indicate that cholesterol-enrichment and plasma lipoproteins enhance vascular contractile response, our results suggest that the cholesterol-enrichment of endothelial cells may also indirectly affect the vascular response via disturbing the function of Na+/K+ pump.

摘要

使用[3H]哇巴因对培养的人脐静脉内皮细胞(huvEC)进行结合实验。饱和研究得出,在无钾缓冲液中,这些细胞上特异性[3H]哇巴因结合的结合容量(Bmax)为820±81飞摩尔/毫克蛋白(n = 4),解离常数(KD)为11.7±2.1纳摩尔(n = 4)。细胞外钾离子以剂量依赖性方式抑制这种结合。Bmax的平均值相当于每个细胞约4×10⁵个位点,与平滑肌细胞相当。这些数据表明存在与Na⁺/K⁺泵相关的特异性[3H]哇巴因结合,这与在huvEC中观察到的哇巴因敏感的⁸⁶Rb摄取一致。还研究了胆固醇富集的影响。在补充有摩尔比为2:1的胆固醇 - 磷脂脂质体的培养基中孵育18小时,使Bmax降低了31%(P < 0.05),而KD值没有显著变化。[3H]哇巴因结合的这种降低似乎对胆固醇具有特异性,因为用纯磷脂制成的脂质体不会改变结合。最近的研究结果表明,胆固醇富集和血浆脂蛋白会增强血管收缩反应,我们的结果表明,内皮细胞的胆固醇富集也可能通过干扰Na⁺/K⁺泵的功能间接影响血管反应。

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