首页> 外文期刊>Cytometry: The Journal of the Society for Analytical Cytology >TOPICAL APPLICATION OF 12-O-TETRADECANOYLPHORBOL-13-ACETATE INDUCES DYSSYNCHRONOUS EXPRESSION OF KERATINS K1 AND K10 IN MOUSE EPIDERMIS
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TOPICAL APPLICATION OF 12-O-TETRADECANOYLPHORBOL-13-ACETATE INDUCES DYSSYNCHRONOUS EXPRESSION OF KERATINS K1 AND K10 IN MOUSE EPIDERMIS

机译:12-邻-四癸基萘酚-13-乙酸酯在小鼠表皮中诱导角蛋白K1和K10表达失调的典型应用

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12-O-tetradecanoylphorbol-13-acetate (TPA) is a potent tumor promoter that causes severe alterations in the biosynthesis of epidermal keratins, This study shows that TPA induces a dyssynchronous effect on keratin expression in stratified squamous epithelium. The effect of TPA on the separate expression of the maturation-associated keratins K1 and K10 was studied by immunohistochemistry in an unperturbed replicative keratinocyte population of hairless mice epidermis in relation to changes in the cell cycle time during regeneration, Keratinocytes in DNA synthesis were pulse-labeled by intraperitoneal injection of the thymidine analogue 5-bromodeoxyuridine (BrdUrd) 1 h before a single topical application of TPA. The BrdUrd-labeled cell cohort, representing an originally unperturbed replicative keratinocyte population exposed to TPA mainly in the postreplicative period, was followed for up to 97 h, The results suggested unaltered timing of the onset of K1 and K10 expression compared with normal epidermis (18 and 24 h, respectively, following DNA synthesis), This indicates that the synthesis of both keratins was programmed before the keratinocytes entered their last DNA. synthesis. A reduction in K10 expression from about 30 h compared with that of K1 expression was observed. Mathematical modeling suggested a delay in K10 expression related to the second and third rounds of cell divisions after pulse-labeling, How TPA induces such dyssynchrony in K1 and K10 regulation remains unknown. (C) 1995 Wiley-Liss, Inc. [References: 22]
机译:12-O-十四烷酰佛波醇13-乙酸盐(TPA)是一种强力的肿瘤促进剂,可引起表皮角蛋白生物合成的严重改变。这项研究表明,TPA诱导分层鳞状上皮细胞中的角蛋白表达有失调作用。通过免疫组织化学在无毛小鼠表皮的无干扰复制角质形成细胞群中研究了TPA对成熟相关的角蛋白K1和K10的独立表达的影响,涉及再生过程中细胞周期的变化,DNA合成中的角质形成细胞是脉冲-在单次局部应用TPA前1小时腹膜内注射胸苷类似物5-溴脱氧尿苷(BrdUrd)进行标记。 BrdUrd标记的细胞队列代表最初在复制后时期暴露于TPA的原本不受干扰的复制性角质形成细胞群体,随访时间长达97 h。结果表明,与正常表皮相比,K1和K10表达的发生时间没有改变(18分别在DNA合成后的24小时和24小时内),这表明在角质形成细胞进入其最后一个DNA之前,已编程了两种角蛋白的合成。合成。与K1表达相比,观察到K10表达从约30小时开始减少。数学模型表明,与脉冲标记后第二和第三轮细胞分裂有关的K10表达延迟。TPA如何在K1和K10调节中诱导这种不同步性仍是未知的。 (C)1995 Wiley-Liss,Inc. [参考:22]

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