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在培养的人角质形成细胞中,1,25 - 二羟基维生素D3的抗增殖和分化活性因表皮生长因子而增强,因胰岛素而减弱。

The antiproliferative and differentiative activities of 1,25-dihydroxyvitamin D3 are potentiated by epidermal growth factor and attenuated by insulin in cultured human keratinocytes.

作者信息

Chen T C, Persons K, Liu W W, Chen M L, Holick M F

机构信息

Vitamin D, Skin and Bone Research Laboratory, Boston University Medical Center, MA 02118.

出版信息

J Invest Dermatol. 1995 Jan;104(1):113-7. doi: 10.1111/1523-1747.ep12613601.

Abstract

1,25-dihydroxyvitamin D3 (1,25(OH)2D3) is a potent inhibitor of keratinocyte proliferation, as well as a stimulator of epidermal terminal differentiation. In the present studies, we investigated the influence of epidermal growth factor (EGF) and insulin on the antiproliferative and differentiation activities of 1,25(OH)2D3. Our results indicate the following: (1) EGF caused a dramatic potentiation of the 1,25(OH)2 D3-induced inhibition of 3H-thymidine incorporation into keratinocytes in a dose-dependent manner; (2) insulin acted antagonistically on the EGF-dependent potentiation of the 1,25(OH)2D3-induced antiproliferative activity; (3) transforming growth factor-alpha potentiated 1,25(OH)2D3-induced antiproliferative activity similar to EGF; (4) the EGF effect was not dependent upon 1,25(OH)2D3 receptor mRNA up-regulation; and (5) removal of insulin from medium supplemented with growth factors significantly potentiated the 1,25(OH)2D3-induced inhibition on the number of basal cells and the 1,25(OH)2D3-dependent cornified envelope formation. In conclusion, the antiproliferative activity of 1,25(OH)2D3 in cultured normal human keratinocytes is greatly enhanced by EGF or transforming growth factor-alpha and reduced by insulin. Insulin also inhibits 1,25(OH)2D3-induced terminal differentiation of cultured normal human keratinocytes.

摘要

1,25 - 二羟基维生素D3(1,25(OH)2D3)是角质形成细胞增殖的强效抑制剂,也是表皮终末分化的刺激剂。在本研究中,我们调查了表皮生长因子(EGF)和胰岛素对1,25(OH)2D3的抗增殖和分化活性的影响。我们的结果表明:(1)EGF以剂量依赖性方式显著增强了1,25(OH)2D3诱导的对角质形成细胞中3H - 胸腺嘧啶核苷掺入的抑制作用;(2)胰岛素对EGF依赖性增强的1,25(OH)2D3诱导的抗增殖活性起拮抗作用;(3)转化生长因子 - α增强1,25(OH)2D3诱导的抗增殖活性,类似于EGF;(4)EGF的作用不依赖于1,25(OH)2D3受体mRNA的上调;(5)从补充有生长因子的培养基中去除胰岛素显著增强了1,25(OH)2D3对基底细胞数量的诱导抑制作用以及1,25(OH)2D3依赖性角质包膜的形成。总之,EGF或转化生长因子 - α可大大增强1,25(OH)2D3在培养的正常人角质形成细胞中的抗增殖活性,而胰岛素则使其降低。胰岛素还抑制1,25(OH)2D3诱导的培养正常人角质形成细胞的终末分化。

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