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生长因子在新生期暴露于己烯雌酚的小鼠阴道上皮持续性增殖诱导中的作用。

Involvement of growth factors in induction of persistent proliferation of vaginal epithelium of mice exposed neonatally to diethylstilbestrol.

作者信息

Sato Tomomi, Fukazawa Yugo, Ohta Yasuhiko, Iguchi Taisen

机构信息

Graduate School of Integrated Science, Yokohama City University, Yokohama 236-0027, Japan.

出版信息

Reprod Toxicol. 2004 Nov;19(1):43-51. doi: 10.1016/j.reprotox.2004.05.004.

Abstract

Neonatal treatment of female mice with natural and synthetic estrogens including diethylstilbestrol (DES) results in persistent proliferation and cornification of vaginal epithelium. In order to study the mechanism of persistent proliferation of vaginal epithelium, histological and biochemical changes were examined in the vagina of C57BL female mice exposed neonatally to 3 microg DES for 5 days. In intact control adult mice, ovariectomy induced apoptotic cell death in vaginal epithelial cells detected by in situ 3'-DNA nick end labeling method accompanied by low DNA synthesis detected by incorporation of bromodeoxyuridine. In neonatally DES-exposed adult mice, however, ovariectomy did not induce reduction of DNA synthesis and showed only a slight increase in apoptotic cells of vaginal epithelium. In neonatally DES-exposed mouse vagina, semi-quantitative reverse transcription polymerase chain reaction revealed a continuous higher expression of mRNAs encoding epidermal growth factor (EGF) and transforming growth factor-alpha (TGF-alpha). These results indicate that neonatal DES exposure causes the increase in expression of EGF and TGF-alpha mRNA, possibly resulting in the induction of persistent proliferation and cornification of vaginal epithelium in mice.

摘要

用包括己烯雌酚(DES)在内的天然和合成雌激素对新生雌性小鼠进行处理,会导致阴道上皮持续增殖和角质化。为了研究阴道上皮持续增殖的机制,对新生期暴露于3微克DES 5天的C57BL雌性小鼠的阴道进行了组织学和生化变化检测。在完整的成年对照小鼠中,卵巢切除术通过原位3'-DNA缺口末端标记法检测到阴道上皮细胞发生凋亡性细胞死亡,同时通过掺入溴脱氧尿苷检测到低水平的DNA合成。然而,在新生期暴露于DES的成年小鼠中,卵巢切除术并未导致DNA合成减少,仅显示阴道上皮凋亡细胞略有增加。在新生期暴露于DES的小鼠阴道中,半定量逆转录聚合酶链反应显示,编码表皮生长因子(EGF)和转化生长因子-α(TGF-α)的mRNA持续高表达。这些结果表明,新生期暴露于DES会导致EGF和TGF-α mRNA表达增加,可能导致小鼠阴道上皮持续增殖和角质化。

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