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去甲肾上腺素可激活人前列腺基质细胞和平滑肌细胞中的P44和P42丝裂原活化蛋白激酶,但对上皮细胞无此作用。

Norepinephrine activates P44 and P42 MAPK in human prostate stromal and smooth muscle cells but not in epithelial cells.

作者信息

Kanagawa Kenji, Sugimura Kazunobu, Kuratsukuri Katsuyuki, Ikemoto Shin-Ichi, Kishimoto Taketoshi, Nakatani Tatsuya

机构信息

Department of Urology, Osaka City University Medical School, Osaka, Japan.

出版信息

Prostate. 2003 Sep 1;56(4):313-8. doi: 10.1002/pros.10267.

Abstract

BACKGROUND

In vascular smooth muscle cells, alpha1-adrenergic stimulation increases DNA synthesis and cell proliferation via activation of p44/42 (ERK1/2) MAPK. We examined whether norepinephrine (NE) activates MAPK and stimulates the proliferation of prostatic epithelial and non-epithelial cells.

METHODS

Human prostatic epithelial cells, stromal cells, and smooth muscle cells were purchased from BioWhittaker (Walkersville, MD). After reaching a semi-confluent condition, the cells were cultured in RPMI-1640 without serum for 1 day. At 10 min after adding NE (10(-6) or 10(-7) M) to the medium, the cells were collected. Cell lysate was analyzed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed by Western blot using anti-phospho-p44/42 and anti-p44/42 antibodies. The activation of p44/42 was estimated by the ratio of phospho-p44/42 to total p44/42. Cell proliferation was evaluated by (3)H-thymidine uptake assay. After reaching a semi-confluent condition, the cells were cultured in RPMI-1640 containing 0.5% FCS with or without NE (10(-6) or 10(-7) M) for 16 hr followed by a (3)H-thymidine uptake period (24 hr).

RESULTS

P44/42 MAPK was significantly activated by NE in non-epithelial cells (stromal cells and smooth muscle cells) while not in epithelial cells. The uptake of (3)H-thymidine was significantly increased by NE in both non-epithelial cells, which was inhibited by alpha1-adrenoceptor antagonists.

CONCLUSIONS

These results suggest that NE may stimulate the proliferation of non-epithelial prostatic cells, which may be involved in the pathogenesis of BPH.

摘要

背景

在血管平滑肌细胞中,α1 - 肾上腺素能刺激通过激活p44/42(ERK1/2)丝裂原活化蛋白激酶(MAPK)增加DNA合成和细胞增殖。我们研究了去甲肾上腺素(NE)是否激活MAPK并刺激前列腺上皮细胞和非上皮细胞的增殖。

方法

人前列腺上皮细胞、基质细胞和平滑肌细胞购自BioWhittaker(马里兰州沃克维尔)。达到半汇合状态后,将细胞在无血清的RPMI - 1640中培养1天。在向培养基中加入NE(10^(-6)或10^(-7) M)10分钟后,收集细胞。细胞裂解物通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS - PAGE)分析,然后使用抗磷酸化p44/42和抗p44/42抗体进行蛋白质印迹分析。通过磷酸化p44/42与总p44/42的比率估计p44/42的活化。通过^3H - 胸腺嘧啶核苷摄取试验评估细胞增殖。达到半汇合状态后,将细胞在含有0.5%胎牛血清且有或无NE(10^(-6)或10^(-7) M)的RPMI - 1640中培养16小时,随后进行^3H - 胸腺嘧啶核苷摄取期(24小时)。

结果

NE在非上皮细胞(基质细胞和平滑肌细胞)中显著激活P44/42 MAPK,而在上皮细胞中未激活。NE在两种非上皮细胞中均显著增加^3H - 胸腺嘧啶核苷的摄取,这被α1 - 肾上腺素能受体拮抗剂抑制。

结论

这些结果表明,NE可能刺激前列腺非上皮细胞的增殖,这可能参与良性前列腺增生的发病机制。

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