DNA ploidy changes in rhino mouse skin induced by all-trans retinoic acid and retinol.

S González, M V Alcaraz, F Díaz, T J Flotte, I Pérez de Vargas, R R Anderson, N Kollias
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引用次数: 5

Abstract

Objective: In order to assess the proliferative changes induced by all-trans retinoic acid (RA) and retinol (ROL), we have carried out a study of the DNA content of basal and suprabasal keratinocytes after epicutaneous application on the rhino mouse.

Study design: Skin sections were analyzed stereologically and cytophotometrically using the Feulgen technique. The diploid DNA value (2C) was obtained from hepatocyte nuclei of control animals. Whereas cells in phase G0-G1 will show a 2C content, cells during phase S and in phase G2-M will show DNA values ranging from 2C to 4C and 4C, respectively.

Results: Although epidermal thickness (ET) increased significantly in all treated animals, surface density only increased in animals treated with all-trans RA. Quantification of DNA content of basal keratinocytes showed reduction of 2C and 2C-4C populations with a commensurate increase in proportions of cells with 4C and > 4C in the animals treated with 0.025% all-trans RA and ROL. Suprabasal keratinocytes of mice treated with 0.025% all-trans showed a decrease of the 2C population and an increased proportion of cells with 4C. Whereas 0.025% all-trans RA induced an increase of both basal and suprabasal DNA indices, ROL enhanced only the basal DNA index significantly.

Conclusion: Animals treated with 0.025% ROL showed a significant increase in the basal proliferative index (PI) while the suprabasal PI remained constant; treatment with 0.025% all-trans RA produced a significant increase of both basal and suprabasal PIs and parakeratotic hyperkeratosis probably due to incomplete differentiation.

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全反式维甲酸和视黄醇诱导的犀牛小鼠皮肤DNA倍体变化。
目的:为了评价全反式维甲酸(RA)和视黄醇(ROL)对犀牛小鼠表皮作用后基底和基底上角质形成细胞的DNA含量的影响。研究设计:采用Feulgen技术对皮肤切片进行立体学和细胞光度分析。对照动物肝细胞核二倍体DNA值(2C)。G0-G1期细胞的DNA含量为2C,而S期和G2-M期细胞的DNA含量分别为2C - 4C和4C。结果:虽然所有治疗动物的表皮厚度(ET)均显著增加,但表面密度仅在全反式RA治疗动物中增加。对基底角质形成细胞DNA含量的定量分析显示,在0.025%全反式RA和ROL处理的动物中,2C和2C-4C群体减少,4C和> 4C的细胞比例相应增加。0.025%全反式处理小鼠的基底上角质形成细胞显示2C群体减少,4C细胞比例增加。0.025%的全反式RA诱导了基础和上基础DNA指数的升高,而ROL仅显著提高了基础DNA指数。结论:0.025% ROL可显著提高基底细胞增殖指数(PI),而基底细胞上增殖指数保持不变;0.025%全反式RA治疗可显著增加基底和基底上pi以及角化不全性角化过度,可能是由于分化不完全。
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