James-Kracke M R, Sloane B F, Shuman H, Karp R, Somlyo A P
J Cell Physiol. 1980 May;103(2):313-22. doi: 10.1002/jcp.1041030217.
Mitochondrial and cytoplasmic composition were determined with electron probe analysis in freeze-dried guinea pig aortic smooth muscle cells cultured on stainless steel grids. The mitochondrial calcium content in normal cells was low: not significantly different from that detected in the cytoplasm. Mitochondrial calcium granules were found in less than 3% of the cells, and in these the cytoplasmic K/Na ratio was reduced, indicating that they were damaged. There were no major differences between the cytoplasmic concentrations of K, Cl, Ca, Mg, and S of cultured cells and those previously found in adult vascular smooth muscle (Somlyo et al '79). There was no evidence of nuclear Na or Ca sequestration in cultured cells, and the transmitochondrial Na, Cl, and K gradients were small. Attempts to selectively remove adhering, extracellular ions with a 2-second wash with isotonic ammonium acetate were unsuccessful because they were accompanied by loss of cell K.
利用电子探针分析测定了培养在不锈钢网格上的冻干豚鼠主动脉平滑肌细胞中的线粒体和细胞质成分。正常细胞中的线粒体钙含量较低:与在细胞质中检测到的钙含量无显著差异。在不到3%的细胞中发现了线粒体钙颗粒,在这些细胞中细胞质的K/Na比值降低,表明它们已受损。培养细胞的细胞质中K、Cl、Ca、Mg和S的浓度与先前在成年血管平滑肌中发现的浓度(Somlyo等人,1979年)没有重大差异。在培养细胞中没有证据表明存在核钠或钙的隔离,并且线粒体间的钠、氯和钾梯度较小。尝试用等渗醋酸铵进行2秒冲洗以选择性去除附着的细胞外离子未成功,因为这会导致细胞钾的流失。