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[大鼠个体发育过程中肝细胞中特定雌激素结合蛋白表达的性别依赖性]

[The sex dependence of the expression of the particular estrogen-binding protein in the hepatocytes in rat ontogeny].

作者信息

Kovtun I V, Smirnova O V

出版信息

Ontogenez. 1993 Sep-Oct;24(5):34-42.

PMID:8233305
Abstract

Formation of dependence on sex of the unusual estrogen-binding protein (UEBP) expression in rat liver during postnatal development was studied using radioligand and immunohistochemical techniques. UEBP was shown to appear in the male and female liver by day 45 to 50 of postnatal life. In females, UEBP remained at a low level until day 75 to 80, corresponding to faint UEBP-specific staining of a single layer of hepatocytes surrounding the central vein. Thereafter UEBP level decreased below the resolving capacity of the method. In males, UEBP content progressively increased during subsequent stages of ontogenesis. This is accompanied by formation of a stable descending centrolobular-periportal gradient of UEBP-positive hepatocytes. High UEBP expression in the male liver was found to result from the programming effect of androgens exerted between days 1-3 and 12 of postnatal development. The formation of hepatic lobuli is not a condition sufficient for switching on the androgen program of UEBP expression. The absence of testicular androgens in males after day 12 of life does not affect the androgen-programmed ontogenetic time course of UEBP expression at high levels. Experimental programming of UEBP expression in hepatocytes of immature females with the use of androgens results in lower UEBP levels than in males. These levels are comparable to those found in male liver at early stages of regeneration (96 h) after partial hepatectomy. It is suggested that androgens determine not only UEBP-producing capacity of hepatocytes but also the system of its control.

摘要

利用放射性配体和免疫组织化学技术,研究了产后发育过程中大鼠肝脏中异常雌激素结合蛋白(UEBP)表达对性别的依赖性形成。结果显示,UEBP在出生后45至50天时出现在雄性和雌性肝脏中。在雌性中,UEBP在75至80天之前一直处于低水平,对应于中央静脉周围单层肝细胞微弱的UEBP特异性染色。此后,UEBP水平降至该方法的检测限以下。在雄性中,UEBP含量在个体发育的后续阶段逐渐增加。这伴随着UEBP阳性肝细胞形成稳定的中央小叶至门静脉递减梯度。发现雄性肝脏中高UEBP表达是由于出生后发育第1至3天和第12天之间雄激素的编程作用。肝小叶的形成并非开启UEBP表达雄激素程序的充分条件。出生后第12天之后雄性睾丸雄激素的缺失并不影响高水平UEBP表达的雄激素编程个体发育时间进程。使用雄激素对未成熟雌性肝细胞中的UEBP表达进行实验性编程,其UEBP水平低于雄性。这些水平与部分肝切除术后再生早期(96小时)雄性肝脏中的水平相当。研究表明,雄激素不仅决定肝细胞产生UEBP的能力,还决定其控制系统。

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