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雌激素介导的大鼠阴道上皮分化过程中角蛋白表达的变化。

Changes in keratin expression during the estrogen-mediated differentiation of rat vaginal epithelium.

作者信息

Kronenberg M S, Clark J H

出版信息

Endocrinology. 1985 Oct;117(4):1480-9. doi: 10.1210/endo-117-4-1480.

DOI:10.1210/endo-117-4-1480
PMID:2411529
Abstract

While vaginal cornification occurs naturally during the estrous cycle of the adult rat, it can also be artificially induced by administering exogenous hormone to ovariectomized animals. When the maturation of rat vaginal epithelium was controlled with a timed course of estradiol (E2) injections, total cell extracts from that tissue revealed that six major keratins exhibited stage-specific increases during a 48-h period of stratification and cornification. One-dimensional polyacrylamide gel electrophoresis and electrophoretic immunoblotting showed that the expression pattern involved an earlier rise of the smaller (50,000, 51,000, and 53,000 mol wt) keratins and a later rise of the larger (57,000, 58,000, and 60,000 mol wt) keratins. Polypeptide levels were quantitated by gel densitometry, and an immunodot assay was developed to specifically measure keratin expression as a function of estrogen agonist activity. By way of comparison, four other estrogenic compounds were also evaluated after their administration under a 48-h double injection protocol. Under these circumstances, diethylstilbestrol provided a more potent stimulus than E2, while estriol, enclomiphene and zuclomiphene each produced a pattern of keratin expression and intensity levels that resembled that 24-h stage of E2 treatment. Although the same keratins were expressed by these different compounds, their synthesis was selective, since they often increased 10- to 20-fold while total protein levels only doubled. Keratin levels were correlated with the various degrees of epithelial growth and differentiation observed in parallel histological studies. These results indicate that the expression of vaginal keratins provide a useful model system for the study of estrogen action.

摘要

虽然成年大鼠在发情周期中阴道角质化会自然发生,但也可以通过给去卵巢动物注射外源激素来人工诱导。当用雌二醇(E2)注射的定时过程来控制大鼠阴道上皮的成熟时,该组织的总细胞提取物显示,在48小时的分层和角质化过程中,六种主要角蛋白呈现出阶段特异性增加。一维聚丙烯酰胺凝胶电泳和免疫印迹电泳表明,表达模式涉及较小分子量(50,000、51,000和53,000道尔顿)角蛋白的早期升高和较大分子量(57,000、58,000和60,000道尔顿)角蛋白的后期升高。通过凝胶密度测定法定量多肽水平,并开发了一种免疫斑点测定法来特异性测量作为雌激素激动剂活性函数的角蛋白表达。作为比较,在48小时双注射方案下给予另外四种雌激素化合物后也进行了评估。在这些情况下,己烯雌酚比E2提供了更强的刺激,而雌三醇、恩氯米芬和氯米芬各自产生的角蛋白表达模式和强度水平类似于E2处理24小时阶段的模式。尽管这些不同的化合物表达相同的角蛋白,但它们的合成是选择性的,因为它们通常增加10至20倍,而总蛋白水平仅增加一倍。角蛋白水平与平行组织学研究中观察到的不同程度的上皮生长和分化相关。这些结果表明,阴道角蛋白的表达为研究雌激素作用提供了一个有用的模型系统。

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Changes in keratin expression during the estrogen-mediated differentiation of rat vaginal epithelium.雌激素介导的大鼠阴道上皮分化过程中角蛋白表达的变化。
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Proliferation and differentiation of prepubertal mouse vaginal epithelial cells in vitro and the specificity of estrogen-induced growth retardation.青春期前小鼠阴道上皮细胞的体外增殖与分化及雌激素诱导生长迟缓的特异性
In Vitro Cell Dev Biol. 1991 Jun;27A(6):461-8. doi: 10.1007/BF02631145.