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霍乱毒素对培养的人角质形成细胞增殖的影响及其与细胞内环磷酸腺苷水平的关系。

Effects of cholera toxin on proliferation of cultured human keratinocytes in relation to intracellular cyclic AMP levels.

作者信息

Okada N, Kitano Y, Ichihara K

出版信息

J Invest Dermatol. 1982 Jul;79(1):42-7. doi: 10.1111/1523-1747.ep12510580.

Abstract

In the culture of epidermal keratinocytes, the cellular growth rate is reported to be accelerated by cholera toxin. The mechanism by which cholera toxin exerts biological effects is thought to result from changes in intracellular cyclic AMP concentrations. But in many reports cyclic AMP elevating agents appeared to inhibit growth of keratinocytes in culture. This study was done to clarify the discrepancy of this problem. Determination of cyclic AMP revealed that cholera toxin over a range of 10-14-10-8 M increased the intracellular concentration of cyclic AMP of cultured keratinocytes about 100-fold over the controls after incubation for 6 hr. When a small number (10(5)) of cells were inoculated in a 60 X 15 mm culture dish, cholera toxin strongly stimulated colony growth. When a relatively larger number (8 X 10(5)) of cells were inoculated in a dish, cholera toxin moderately accelerated cell division, and increased DNA and protein levels of the culture during early days of cultivation. But after about 20 days, of cultivation when the culture reached confluence, cholera toxin decreased both DNA and protein content in a culture dish. The cultures were pulse labeled with 3H-thyrmidine at 12 and 24 hr after the addition of 10-10 M cholera toxin, and its uptake into DNA was determined. In the early days of cultivation the uptake of 3H-thymidine increased after treatment with cholera toxin. But in the late days of cultivation, cholera toxin decreased the rate of 3H-thymidine incorporation into DNA. These results indicated that cholera toxin-cyclic AMP has effects on the proliferation of keratinocytes in culture biphasically according to cellular concentrations in culture.

摘要

在表皮角质形成细胞培养中,据报道霍乱毒素可加速细胞生长速率。霍乱毒素发挥生物学效应的机制被认为是细胞内环磷酸腺苷(cAMP)浓度变化所致。但在许多报道中,cAMP升高剂似乎会抑制培养的角质形成细胞生长。本研究旨在阐明这一问题的差异。cAMP的测定显示,在10⁻¹⁴ - 10⁻⁸ M范围内的霍乱毒素,在孵育6小时后,使培养的角质形成细胞内cAMP浓度比对照组增加约100倍。当将少量(10⁵)细胞接种于60×15 mm培养皿中时,霍乱毒素强烈刺激集落生长。当将相对大量(8×10⁵)细胞接种于培养皿中时,霍乱毒素适度加速细胞分裂,并在培养早期增加培养物中的DNA和蛋白质水平。但在培养约20天后,当培养物达到汇合时,霍乱毒素降低了培养皿中DNA和蛋白质含量。在添加10⁻¹⁰ M霍乱毒素后的12小时和24小时,用³H - 胸腺嘧啶对培养物进行脉冲标记,并测定其掺入DNA的情况。在培养早期,用霍乱毒素处理后³H - 胸腺嘧啶的掺入增加。但在培养后期,霍乱毒素降低了³H - 胸腺嘧啶掺入DNA的速率。这些结果表明,霍乱毒素 - cAMP根据培养物中的细胞浓度对培养的角质形成细胞增殖具有双相作用。

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