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腺苷可刺激培养的人内皮细胞增殖。

Adenosine stimulates proliferation of human endothelial cells in culture.

作者信息

Ethier M F, Chander V, Dobson J G

机构信息

Department of Medicine, University of Massachusetts Medical School, Worcester 01655.

出版信息

Am J Physiol. 1993 Jul;265(1 Pt 2):H131-8. doi: 10.1152/ajpheart.1993.265.1.H131.

Abstract

The effect of adenosine on proliferation of human endothelial cells was investigated by adding adenosine to the medium of cultures derived from human umbilical veins. Cell counts on cultures grown in 10 microM adenosine for 4-7 days were 41-53% greater than counts from control cultures. In contrast, 10 microM adenosine had no effect on growth of a human fibroblast cell strain (IMR-90). Neither inosine nor 2',5'-dideoxyadenosine influenced endothelial cell growth at concentrations of 0.1 or 10 microM. Addition of adenosine deaminase abolished the proliferative effect of added adenosine and inhibited proliferation by 16% in control cultures, suggesting that endogenous adenosine may enhance proliferation in culture. The adenosine receptor antagonist, 8-phenyltheophylline, at 0.1 and 1.0 microM blocked the enhanced proliferation caused by 10 microM adenosine. Addition of 10 microM adenosine enhanced DNA synthesis in endothelial cell cultures as indicated by an increased incorporation of [3H]thymidine into acid-insoluble cell material. The results indicate that addition of physiological concentrations of adenosine to human umbilical vein endothelial cell cultures stimulates proliferation, possibly via a surface receptor, and suggest that adenosine may be a factor for human endothelial cell growth and possibly angiogenesis.

摘要

通过向源自人脐静脉的培养物培养基中添加腺苷,研究了腺苷对人内皮细胞增殖的影响。在含有10微摩尔腺苷的培养基中培养4至7天的细胞计数比对照培养物的细胞计数高41%至53%。相比之下,10微摩尔腺苷对人成纤维细胞系(IMR-90)的生长没有影响。在0.1或10微摩尔浓度下,肌苷和2',5'-二脱氧腺苷均不影响内皮细胞生长。添加腺苷脱氨酶消除了添加的腺苷的增殖作用,并使对照培养物中的增殖受到16%的抑制,这表明内源性腺苷可能增强培养物中的增殖。腺苷受体拮抗剂8-苯基茶碱在0.1和1.0微摩尔浓度下可阻断由10微摩尔腺苷引起的增殖增强。添加10微摩尔腺苷可增强内皮细胞培养物中的DNA合成,这通过[3H]胸苷掺入酸不溶性细胞物质的增加来表明。结果表明,向人脐静脉内皮细胞培养物中添加生理浓度的腺苷可刺激增殖,可能是通过表面受体实现的,并表明腺苷可能是人类内皮细胞生长以及可能的血管生成的一个因素。

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