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岩沙海葵毒素对人成骨样Saos-2细胞中钠和钙稳态的作用。

Actions of palytoxin on Na+ and Ca2+ homeostasis in human osteoblast-like Saos-2 cells.

作者信息

Monroe J J, Tashjian A H

机构信息

Department of Molecular and Cellular Toxicology, Harvard School of Public Health, Boston, Massachusetts, USA.

出版信息

Am J Physiol. 1995 Sep;269(3 Pt 1):C582-9. doi: 10.1152/ajpcell.1995.269.3.C582.

Abstract

Palytoxin (PTx) is a potent membrane-active agent produced by marine coelenterates that acts to stimulate bone resorption in organ culture at nanomolar concentrations. We report here the actions of PTx on Na+ and Ca2+ homeostasis in human osteoblast-like Saos-2 cells. PTx induced a rise in the cytosolic free Na+ concentration ([Na]i) by causing entry of extracellular Na+ (Na(e)+). PTx also caused a concentration-dependent biphasic rise in the cytosolic free Ca2+ concentration ([Ca2+]i) by enhancing entry of extracellular Ca2+ (Ca(e)2+). Entry of Na+ was dependent on the presence of Ca(e)2+ and was prevented by the Na+/Ca2+ exchange antagonist 3,4-dichlorobenzamil (DCB). Entry of Ca2+ was dependent on the presence of Na(e)+ but was not prevented by DCB. The actions of PTx on [Na+]i and [Ca2+]i were completely inhibited by pretreatment of the cells with ouabain. Ouabain alone had no acute effect on [Na+]i or [Ca2+]i in Saos-2 cells. We propose that interaction of PTx with the Na+ pump created a channel that allowed influx of Na(e)+ and Ca(e)2+. The rise in [Ca2+]i then stimulated the activity of the plasma membrane Na+/Ca2+ exchanger, which further enhanced Na(e)+ entry.

摘要

刺尾鱼毒素(PTx)是一种由海洋腔肠动物产生的强效膜活性剂,在纳摩尔浓度下可刺激器官培养中的骨吸收。我们在此报告PTx对人成骨样Saos-2细胞中Na⁺和Ca²⁺稳态的作用。PTx通过引起细胞外Na⁺(Na(e)⁺)的内流,导致胞质游离Na⁺浓度([Na]i)升高。PTx还通过增强细胞外Ca²⁺(Ca(e)²⁺)的内流,引起胞质游离Ca²⁺浓度([Ca²⁺]i)呈浓度依赖性双相升高。Na⁺的内流依赖于Ca(e)²⁺的存在,并被Na⁺/Ca²⁺交换拮抗剂3,4-二氯苯甲酰胺(DCB)所阻断。Ca²⁺的内流依赖于Na(e)⁺的存在,但不受DCB的阻断。用哇巴因预处理细胞可完全抑制PTx对[Na⁺]i和[Ca²⁺]i的作用。单独使用哇巴因对Saos-2细胞中的[Na⁺]i或[Ca²⁺]i没有急性影响。我们提出,PTx与Na⁺泵的相互作用产生了一个通道,允许Na(e)⁺和Ca(e)²⁺内流。[Ca²⁺]i的升高随后刺激了质膜Na⁺/Ca²⁺交换器的活性,这进一步增强了Na(e)⁺的内流。

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