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高密度脂蛋白增强人类血小板中的钠/氢逆向转运蛋白。

High density lipoproteins enhance the Na+/H+ antiport in human platelets.

作者信息

Nofer J R, Tepel M, Kehrel B, Walter M, Seedorf U, Assmann G, Zidek W

机构信息

Institut für Klinische Chemie und Laboratoriumsmedizin, Zentrallaboratorium, Münster, Germany.

出版信息

Thromb Haemost. 1996 Apr;75(4):635-41.

PMID:8743192
Abstract

In the present study, we investigated the effect of high density lipoproteins 3 (HDL3) on Na+/H+ exchanger activity and cytosolic pH (pHi) in human platelets. HDL3 alone failed to affect pHi, but preincubation with HDL3 significantly enhanced the Na+/H+ antiport activation brought about by acidification with 100 mM sodium propionate or stimulation with 0.05 U/ml thrombin. the stimulatory effect of HDL3 was unaffected by indomethacin excluding a role for cyclooxygenase products. The HDL3 effect was not mediated by Ca2+/calmodulin-dependent protein kinase as HDL3 failed to increase cytosolic free calcium concentration. However, the potentiating effect of HDL3 was completely blocked in the presence of the protein kinase C inhibitor, bisindoylmaleimide and the phosphatidylcholine-specific phospholipase C inhibitor, D609. Furthermore, the effect of HDL3 was abolished after covalent modification of HDL3 with dimethylsuberimidate and was not observed in platelets from Glanzmann thrombasthenia type 1 which do not express GP IIb/IIIa, as well as in platelets preincubated with anti-GP IIb/IIIa polyclonal antibodies. We conclude that HDL3 enhances the sodium propionate- and thrombin-induced Na+/H+ antiport activity in human platelets via binding to GP IIb/IIIa and activation of protein kinase C and phosphatidylcholine-specific phospholipase C.

摘要

在本研究中,我们调查了高密度脂蛋白3(HDL3)对人血小板中Na+/H+交换活性和细胞内pH值(pHi)的影响。单独的HDL3未能影响pHi,但用HDL3预孵育可显著增强由100 mM丙酸钠酸化或0.05 U/ml凝血酶刺激所引起的Na+/H+反向转运激活。HDL3的刺激作用不受吲哚美辛影响,排除了环氧化酶产物的作用。HDL3的作用不是由Ca2+/钙调蛋白依赖性蛋白激酶介导的,因为HDL3未能增加细胞内游离钙浓度。然而,在蛋白激酶C抑制剂双吲哚马来酰亚胺和磷脂酰胆碱特异性磷脂酶C抑制剂D609存在的情况下,HDL3的增强作用被完全阻断。此外,用辛二酸二甲酯对HDL3进行共价修饰后,HDL3的作用消失,并且在不表达糖蛋白IIb/IIIa的1型Glanzmann血小板无力症患者的血小板中以及在用抗糖蛋白IIb/IIIa多克隆抗体预孵育的血小板中未观察到该作用。我们得出结论,HDL3通过与糖蛋白IIb/IIIa结合以及激活蛋白激酶C和磷脂酰胆碱特异性磷脂酶C来增强人血小板中丙酸钠和凝血酶诱导的Na+/H+反向转运活性。

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