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脂蛋白对培养的人内皮细胞中前列环素、血管性血友病因子及载脂蛋白A-I和A-II合成的影响。

The effect of lipoproteins on the synthesis of prostacyclin, von Willebrand factor and apolipoproteins A-I and A-II in cultured human endothelial cells.

作者信息

Nordøy A, Killie J E, Badimon L, Fass D N, Mao S J, Maciejko J J

出版信息

Atherosclerosis. 1984 Mar;50(3):307-23. doi: 10.1016/0021-9150(84)90078-9.

DOI:10.1016/0021-9150(84)90078-9
PMID:6424692
Abstract

Primary cultures of confluent human endothelial cells (ECM) were grown in media containing the major lipoproteins (LP) and lipoprotein deficient serum (LDS). The release of 6-keto-PGF1 alpha, von Willebrand factor (VIII RAg) and apolipoproteins (apo) A-I and A-II were investigated by radioimmunoassay. The cell-associated VIII RAg, apo A-I and apo A-II were also confirmed by fluorescein antibodies, and the synthesis of the apolipoproteins was examined by incorporation of [3H]leucine. Apo A-I and apo A-II were located and synthesized in ECM, yet only apo A-I was released into the medium. Very low density (VLDL) and low density lipoproteins (LDL) in concentrations of 50-600 micrograms/ml stimulated release of apo A-I. Stimulation of ECM for 5 min with thrombin (T) or arachidonic acid (A) did not induce apo A-I release. VIII RAg was always released into the media from ECM. The release was not affected by the lipoproteins. VIII RAg was also localized on the cell surface (VIII RAgC) and approximately 80% was released by trypsin. LDL stimulated the occurrence of factor VIII RAg on the cell surface. 6-Keto PGF1 alpha was always released into the medium and the production was stimulated by T and AA. The main lipoproteins (50-600 micrograms/ml) and apo A-I and A-II did not affect the release of 6-keto-PGF1 alpha. This study shows that endothelial cells synthesize and release proteins important for thrombogenesis and atherosclerosis. The release of apolipoproteins A-I was stimulated by VLDL and LDL, and the concentration of cell-related factor VIII RAg was stimulated by LDL.

摘要

将汇合的人内皮细胞(ECM)原代培养物在含有主要脂蛋白(LP)和无脂蛋白血清(LDS)的培养基中培养。通过放射免疫测定法研究了6-酮-前列环素F1α、血管性血友病因子(VIII RAg)以及载脂蛋白(apo)A-I和A-II的释放情况。还通过荧光素抗体证实了细胞相关的VIII RAg、apo A-I和apo A-II,并通过掺入[3H]亮氨酸来检测载脂蛋白的合成。apo A-I和apo A-II在内皮细胞中定位并合成,但只有apo A-I释放到培养基中。浓度为50 - 600微克/毫升的极低密度脂蛋白(VLDL)和低密度脂蛋白(LDL)刺激了apo A-I的释放。用凝血酶(T)或花生四烯酸(A)刺激内皮细胞5分钟未诱导apo A-I释放。VIII RAg总是从内皮细胞释放到培养基中。其释放不受脂蛋白影响。VIII RAg也定位于细胞表面(VIII RAgC),约80%可被胰蛋白酶释放。LDL刺激细胞表面因子VIII RAg的出现。6-酮-前列环素F1α总是释放到培养基中,其产生受T和AA刺激。主要脂蛋白(50 - 600微克/毫升)以及apo A-I和A-II不影响6-酮-前列环素F1α的释放。这项研究表明内皮细胞合成并释放对血栓形成和动脉粥样硬化很重要的蛋白质。apo A-I的释放受VLDL和LDL刺激,细胞相关因子VIII RAg的浓度受LDL刺激。

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