肿瘤启动子12- o - tetradecanoylphorol -13-acetate (TPA)促进大鼠腭上皮细胞分化标志物的表达。

D Arenholt, E Dabelsteen
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引用次数: 0

摘要

用不同剂量的强效肿瘤促进剂12- o -十四烷醇-13-乙酸酯(TPA)处理在胶原筏上培养的大鼠腭上皮。加入TPA后1、6、24、48小时的活检切片,检测血型抗原H抗体和抗角蛋白抗体AE1染色的定位。在对照培养中,抗原H只出现在第二和第三细胞层的细胞膜上,与之相反,在tpa处理的标本的基底细胞层中发现了几个抗原H阳性细胞,其中一些呈组状出现。用AE1抗角蛋白抗体对角蛋白进行染色,在对照组中基底细胞没有染色,只有基底上细胞染色,而在tpa处理的培养物中,基底细胞层的几个细胞被该抗体染色呈阳性。这些结果支持了TPA通过迫使一部分基底细胞群体向终末分化而强烈影响基底细胞群体组成的理论。
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The tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA) accelerates expression of differentiation markers in cultures of rat palatal epithelial cells.

Cultures of rat palatal epithelium grown on collagen rafts were treated with different doses of the potent tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA). Sections from biopsies taken 1, 6, 24, and 48 hr after the addition of TPA were examined for the localization of staining by blood group antigen H antibody and antikeratin antibody AE1. In contrast to control cultures, where antigen H was seen exclusively at the cell membranes of the second and third cell layer, several antigen H-positive cells, some appearing in groups, were found in the basal cell layer of TPA-treated specimens. Staining for keratins with the AE1 antikeratin antibody showed no staining of basal cells but only suprabasal cells in controls, whereas several cells of the basal cell layer of TPA-treated cultures stained positively with this antibody. The results support the theory that TPA, by forcing a part of the basal cell population to terminal differentiation, strongly affects the composition of the basal cell population.

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