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Rh 缺乏型红细胞中的磷脂酰丝氨酸暴露与氨基磷脂转运酶活性

Phosphatidylserine exposure and aminophospholipid translocase activity in Rh-deficient erythrocytes.

作者信息

Geldwerth D, Cherif-Zahar B, Helley D, Gane P, Freyssinet J M, Colin Y, Devaux P F, Cartron J P

机构信息

IBPC, Paris, France.

出版信息

Mol Membr Biol. 1997 Jul-Sep;14(3):125-32. doi: 10.3109/09687689709048172.

Abstract

Endogenous phosphatidylserine (PS) exposure and lipid transport activity have been investigated for seven unrelated cases of Rhnull erythrocytes. Endogenous PS exposure was measured by prothrombinase activity. Out of six cases studied, two Rhnull samples exhibited abnormal aminophospholipid exposure, as suggested by the measurement of a lower Km of factor Xa for prothrombin. Aminophospholipid translocase activity was measured through the transbilayer redistribution of spin-labelled analogues of phospholipids. Provided that incubation conditions allow the maintainance of intracellular ATP level, no difference was observed between Rhnull and control erythrocytes, clearly indicating that the aminophospholipid translocase and Rh polypeptides are different molecular species.

摘要

已对7例无亲缘关系的Rhnull红细胞病例的内源性磷脂酰丝氨酸(PS)暴露和脂质转运活性进行了研究。通过凝血酶原酶活性测量内源性PS暴露。在所研究的6例病例中,如通过测量凝血酶原对因子Xa的较低Km值所表明的,两个Rhnull样本表现出异常的氨基磷脂暴露。通过磷脂自旋标记类似物的跨膜重分布来测量氨基磷脂转位酶活性。只要孵育条件能够维持细胞内ATP水平,在Rhnull红细胞和对照红细胞之间未观察到差异,这清楚地表明氨基磷脂转位酶和Rh多肽是不同的分子种类。

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