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首页> 外文期刊>The Prostate >Norepinephrine activates P44 and P42 MAPK in human prostate stromal and smooth muscle cells but not in epithelial cells.
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Norepinephrine activates P44 and P42 MAPK in human prostate stromal and smooth muscle cells but not in epithelial cells.

机译:去甲肾上腺素激活人前列腺基质和平滑肌细胞中的P44和P42 MAPK,但不激活上皮细胞。

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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. Prostate 56: 313-318, 2003.
机译: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)MAPK促进DNA合成和细胞增殖。我们检查了去甲肾上腺素(NE)是否激活MAPK并刺激前列腺上皮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(Walkersville,MD)。达到半融合状态后,将细胞在无血清的RPMI-1640中培养1天。将NE(10(-6)或10(-7)M)加入培养基后10分钟,收集细胞。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE),然后使用抗磷酸化p44 / 42和抗p44 / 42抗体进行蛋白质印迹,分析细胞裂解液。通过磷酸-p44 / 42与总p44 / 42的比率来估计p44 / 42的活化。通过(3)H-胸苷摄取测定法评价细胞增殖。达到半融合状态后,将细胞在含0.5%FCS的RPMI-1640中培养,含或不含NE(10(-6)或10(-7)M)16小时,然后加(3)H-胸苷吸收期(24小时)。结果:P44 / 42 MAPK在非上皮细胞(基质细胞和平滑肌细胞)中被NE显着激活,而在上皮细胞中则未被激活。在两个非上皮细胞中,NE均显着增加了(3)H-胸苷的摄取,这被α1-肾上腺素受体拮抗剂抑制。结论:这些结果提示NE可能刺激非上皮性前列腺细胞的增殖,这可能与BPH的发病机制有关。前列腺56:313-318,2003年。

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