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雄激素对LNCaP人前列腺癌细胞中前列腺酸性磷酸酶表达和分泌的调控

Regulation of prostatic acid phosphatase expression and secretion by androgen in LNCaP human prostate carcinoma cells.

作者信息

Lin M F, Garcia-Arenas R, Chao Y C, Lai M M, Patel P C, Xia X Z

机构信息

Department of Urology, University of Southern California School of Medicine, Los Angeles 90033.

出版信息

Arch Biochem Biophys. 1993 Jan;300(1):384-90. doi: 10.1006/abbi.1993.1052.

Abstract

The expression and the secretion of human prostatic acid phosphatase (PAcP), a differentiation antigen which is the major acid phosphatase in prostate epithelial cells, are thought to be regulated by an androgen. We investigated this regulatory mechanism at the post-transcriptional level in LNCaP human prostate carcinoma cells using a cDNA clone for the secretory form of PAcP. 5 alpha-Dihydrotestosterone (DHT, an active form of endogenous androgen) stimulated the secretion of PAcP from cells grown in a steroid-reduced medium and in a defined serum-free medium, respectively. The secreted PAcP activity was increased following a DHT dose in a dose-dependent fashion at concentrations of up to 1 microM. Further, the stimulation of PAcP secretion occurred following the period of exposure to DHT. During a 5-day treatment period, with 10 nM of DHT in the steroid-reduced medium, the secretion of PAcP was stimulated approximately 150% over that from control cells. Nevertheless, PAcP was secreted from cells grown in the absence of added DHT. First, the androgen dependency of PAcP expression was examined. The expression and the secretion of PAcP were observed in cells that were grown in a defined serum-free medium and grown in a steroid-reduced medium, in the absence of DHT. The increased secretion by DHT was further demonstrated to be in part due to an increase in PAcP mRNA level, as evidenced by Northern blot analysis. PAcP mRNA levels were elevated approximately 2-fold and corresponded to an increase of approximately 2.5-fold in the secreted level of newly synthesized 35S-PAcP. Then, the effect of DHT on the secretory process was investigated. Results of pulse-chase labeling experiments indicated that the secretory rate of PAcP was stimulated by about 50% on average by DHT. In conclusion, our data demonstrated that, in LNCaP cells, the expression and the secretion of PAcP regulated by androgen are apparently hormone-responsive processes. Further, DHT stimulation of PAcP secretion operates within at least two levels: increased PAcP mRNA and stimulation of the secretory pathway.

摘要

人前列腺酸性磷酸酶(PAcP)是前列腺上皮细胞中的主要酸性磷酸酶,属于一种分化抗原,其表达和分泌被认为受雄激素调控。我们使用PAcP分泌形式的cDNA克隆,在转录后水平研究了LNCaP人前列腺癌细胞中的这种调控机制。5α-二氢睾酮(DHT,内源性雄激素的活性形式)分别刺激了在类固醇减少培养基和限定无血清培养基中生长的细胞分泌PAcP。在高达1μM的浓度下,分泌的PAcP活性随DHT剂量呈剂量依赖性增加。此外,PAcP分泌的刺激发生在暴露于DHT之后。在类固醇减少的培养基中用10 nM DHT进行为期5天的处理期间,PAcP的分泌比对照细胞刺激了约150%。然而,在未添加DHT的情况下生长的细胞也会分泌PAcP。首先,检测了PAcP表达的雄激素依赖性。在限定无血清培养基和类固醇减少培养基中生长且无DHT的细胞中观察到了PAcP的表达和分泌。Northern印迹分析表明,DHT导致的分泌增加部分归因于PAcP mRNA水平的升高。PAcP mRNA水平升高了约2倍,相应地新合成的35S-PAcP分泌水平增加了约2.5倍。然后,研究了DHT对分泌过程的影响。脉冲追踪标记实验结果表明,DHT平均刺激PAcP的分泌率约50%。总之,我们的数据表明,在LNCaP细胞中,雄激素调控的PAcP表达和分泌显然是激素反应性过程。此外,DHT对PAcP分泌的刺激至少在两个水平起作用:增加PAcP mRNA和刺激分泌途径。

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