VIP stimulates proliferation and differentiation of the cultured retinal pigment epithelium with disparate potencies

Shay-Whey M. Koh, Gregory J. Kane
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引用次数: 27

Abstract

Previous studies showed that VIP modulates mediators of two signal transduction pathways, namely the adenylate cyclase and the nonreceptor tyrosine protein kinase pp60c-src in cultured chick retinal pigment epithelium (RPE). Here we show that VIP modulates simultaneously two disparate cellular events, namely the cell proliferation and differentiation of the RPE, however, with different potencies. The maximal effects on proliferation and differentiation are observed at 5 × 10−9M and 5 × 10−7M, respectively. Treatment with the maximally effective concentrations of VIP for 10 days increases the cell numbers and the melanin contents to 150% and 200% of the controls, respectively. The lowest concentrations of VIP showing significant stimulatory effect on cell proliferation and melanin synthesis are 5 × 10−11 M and 5 × 10−9M, respectively.

VIP刺激培养的视网膜色素上皮的增殖和分化,具有不同的效力
前期研究表明,VIP可调节培养鸡视网膜色素上皮(RPE)中腺苷酸环化酶和非受体酪氨酸蛋白激酶pp60c-src两种信号转导通路的介质。在这里,我们发现VIP同时调节两个不同的细胞事件,即RPE的细胞增殖和分化,然而,具有不同的效力。在5 × 10−9M和5 × 10−7M时,对细胞增殖和分化的影响最大。以最大有效浓度VIP处理10 d,细胞数量和黑色素含量分别增加到对照的150%和200%。对细胞增殖和黑色素合成有显著刺激作用的VIP最低浓度分别为5 × 10−11 M和5 × 10−9M。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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