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X-537A离子载体介导的普雷斯曼细胞中的钙转运和磷酸钙形成。

X-537A ionophore-mediated calcium transport and calcium phosphate formation in Pressman cells.

作者信息

Eanes E D, Costa J L

出版信息

Calcif Tissue Int. 1983;35(2):250-7. doi: 10.1007/BF02405039.

Abstract

The present study examined precipitate development induced in phosphate solutions by the ionophoric translocation of Ca2+ across a bulk organic solvent barrier. Experiments were conducted at pH 7.4 and 25 or 37 degrees in a three-compartment Pressman cell. The aqueous reaction (0, 2.2 or 22 mM phosphate, 100 mM K+) and donor (1.3 or 13 mM Ca2+, 0.8 mM Mg2+, 100 mM Na+) compartments were separated by a CHCl3 compartment rendered permeable to cations by the addition of the carboxylic ionophore X-537A (2 or 20 mM). The resultant cation movements increased Ca2+, Mg2+, and Na+ concentrations in the reaction compartment at the expense of K+ loss to the donor compartment. The magnitude of the K+ counterflow and the efficiency of the ionophore-mediated Ca2+ in equilibrium 2K+ exchange reaction resulted in appreciable Ca2+ overshoots in the reaction compartment. In the absence of phosphate, Ca2+ increases exceeded donor levels by several-fold. With phosphate present, the Ca2+ flux was sufficient to induced precipitation. Generally, the first solid formed was amorphous. The amorphous precipitate, however, was unstable and converted to an apatite-like crystalline phase. Both carbonate (26 mM) and Mg2+ (0.8 mM) in the reaction solution delayed but did not prevent the conversion. The possible relevance of these findings to matrix vesicle calcification is discussed.

摘要

本研究考察了通过Ca2+跨大量有机溶剂屏障的离子载体转运在磷酸盐溶液中诱导的沉淀形成。实验在三室普雷斯曼细胞中于pH 7.4以及25或37摄氏度下进行。通过添加羧酸离子载体X-537A(2或20 mM)使氯仿室对阳离子具有通透性,从而将水相反应室(0、2.2或22 mM磷酸盐,100 mM K+)和供体室(1.3或13 mM Ca2+,0.8 mM Mg2+,100 mM Na+)分隔开。由此产生的阳离子移动增加了反应室中的Ca2+、Mg2+和Na+浓度,代价是K+向供体室流失。K+逆流的幅度以及离子载体介导的Ca2+在平衡2K+交换反应中的效率导致反应室中Ca2+出现明显的过冲。在没有磷酸盐的情况下,Ca2+的增加超过供体水平数倍。存在磷酸盐时,Ca2+通量足以诱导沉淀。一般来说,首先形成的固体是无定形的。然而,无定形沉淀不稳定,会转化为类磷灰石结晶相。反应溶液中的碳酸盐(26 mM)和Mg2+(0.8 mM)都会延迟但不会阻止这种转化。讨论了这些发现与基质小泡钙化的可能相关性。

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