Whitsett J A, Tsang R C
Pediatr Res. 1980 May;14(5):769-75. doi: 10.1203/00006450-198005000-00012.
An ATP-dependent calcium (Ca2+) sequestration activity was demonstrated in membrane vesicles prepared from the human term placenta. Microsomal and brush border membrane fractions accumulated Ca2+ within a vesicular space by a saturable process requiring Mg2+ and ATP. The "uptake" activity was enriched six-fold in a microsomal membrane fraction and was only 1.5-fold enriched in purified brush border membranes compared to the activity present in the filtered homogenate. Mitochondrial inhibitors such as azide and oligomycin did not inhibit Ca2+ uptake in these preparations. The process was temperature dependent and displayed Michaelis-Menten-like kinetics with respect to free Ca2+ concentrations. At 30 degrees C, the Vmax was 1.05 nmole/mg/min; Km = 74 nM for free Ca2+ in the microsomal fraction. Oxalate and phosphate enhanced uptake in both fractions. Ca2+ uptake activity was not associated with Ca2+-stimulated ATPase, alkaline phosphatase, or other brush border markers during cell fractionation. The characteristics of the Ca2+ uptake process contrasted sharply with those of Ca2+-stimulated ATPase, and a Ca2+-stimulated, Mg2+-dependent ATPase activity could not be identified in these membrane vesicle preparations.
在从足月人胎盘制备的膜囊泡中证实了一种依赖ATP的钙(Ca2+)螯合活性。微粒体和刷状缘膜部分通过一个需要Mg2+和ATP的可饱和过程在囊泡空间内积累Ca2+。与过滤后的匀浆中的活性相比,微粒体膜部分的“摄取”活性富集了6倍,而在纯化的刷状缘膜中仅富集了1.5倍。叠氮化物和寡霉素等线粒体抑制剂在这些制剂中不抑制Ca2+摄取。该过程依赖温度,并且相对于游离Ca2+浓度表现出米氏动力学。在30℃时,微粒体部分中游离Ca2+的Vmax为1.05纳摩尔/毫克/分钟;Km = 74纳摩尔。草酸盐和磷酸盐增强了两个部分的摄取。在细胞分级分离过程中,Ca2+摄取活性与Ca2+刺激的ATP酶、碱性磷酸酶或其他刷状缘标记物无关。Ca2+摄取过程的特征与Ca2+刺激的ATP酶的特征形成鲜明对比,并且在这些膜囊泡制剂中未鉴定出Ca2+刺激的、Mg2+依赖的ATP酶活性。