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钙网蛋白:一种细胞内钙离子结合蛋白,在前列腺上皮细胞中大量表达并受雄激素调节。

Calreticulin: an intracellular Ca++-binding protein abundantly expressed and regulated by androgen in prostatic epithelial cells.

作者信息

Zhu N, Pewitt E B, Cai X, Cohn E B, Lang S, Chen R, Wang Z

机构信息

Department of Urology, Northwestern University Medical School, Chicago, Illinois 60611, USA.

出版信息

Endocrinology. 1998 Oct;139(10):4337-44. doi: 10.1210/endo.139.10.6242.

Abstract

Calreticulin was identified in a screen for androgen-response genes in the rat ventral prostate. Northern blot and Western blot analyses in the rat model showed that both calreticulin messenger RNA and protein are down-regulated by castration and up-regulated by androgen replacement in the prostate. Northern blot analysis showed that calreticulin expression level in the prostate is much higher than that in seminal vesicles, heart, brain, muscle, kidney, and liver. The regulation of calreticulin expression by androgen is only observed in the prostate and seminal vesicles, two male secondary sex organs. The induction of calreticulin by androgen in prostate organ culture partially resists protein synthesis inhibition, suggesting that calreticulin is a direct androgen-response gene. In situ hybridization and immunohistochemistry studies showed that calreticulin is an intracellular protein in prostatic epithelial cells. Because calreticulin is a major intracellular Ca++-binding protein with 1 high-affinity and 25 low-affinity Ca binding sites, our observations suggest that calreticulin is a promising candidate that mediates androgen regulation of intracellular Ca++ levels and/or signals in prostatic epithelial cells. The expression of calreticulin is also regulated by androgen in the mouse and human prostate, suggesting that androgen regulation and function of calreticulin in the prostate are conserved evolutionarily.

摘要

在对大鼠腹侧前列腺雄激素反应基因的筛选中鉴定出了钙网蛋白。大鼠模型中的Northern印迹和Western印迹分析表明,前列腺中的钙网蛋白信使核糖核酸和蛋白质在去势后均下调,而在雄激素替代后上调。Northern印迹分析表明,前列腺中钙网蛋白的表达水平远高于精囊、心脏、大脑、肌肉、肾脏和肝脏中的表达水平。雄激素对钙网蛋白表达的调节仅在前列腺和精囊这两个雄性附属性器官中观察到。雄激素在前列腺器官培养中对钙网蛋白的诱导部分抵抗蛋白质合成抑制,这表明钙网蛋白是一个直接的雄激素反应基因。原位杂交和免疫组织化学研究表明,钙网蛋白是前列腺上皮细胞中的一种细胞内蛋白。由于钙网蛋白是一种主要的细胞内Ca++结合蛋白,具有1个高亲和力和25个低亲和力Ca结合位点,我们的观察结果表明,钙网蛋白是介导雄激素对前列腺上皮细胞内Ca++水平和/或信号调节的一个有前景的候选蛋白。钙网蛋白的表达在小鼠和人类前列腺中也受雄激素调节,这表明雄激素对前列腺中钙网蛋白的调节及其功能在进化上是保守的。

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