Matsubara A
Department of Urology, Hiroshima University School of Medicine.
Nihon Hinyokika Gakkai Zasshi. 1995 May;86(5):1034-43. doi: 10.5980/jpnjurol1989.86.1034.
Stromal-epithelial cell interaction is very important for the development of human benign prostatic hyperplasia (BPH). Growth factors and their receptors in the prostate are thought to mediate the cell communication and play some roles in the development of BPH. Among many growth factors, fibroblast growth factor (FGF) family members have received the most intensive study, and mRNAs for acidic FGF (aFGF), basic FGF (bFGF) and keratinocyte growth factor (KGF) have been identified in rat or human prostate. However, synthesis sites and roles of them in stromal-epithelial cell interaction remain to be undefined. In the present study, to define the mechanisms for the regulation of prostatic cell growth by stromal cells in human BPH, we established the method for isolation and culture of epithelial cells as well as stromal cells from human BPH tissue. Using these primary cultured prostatic cells, we evaluated the effects of stromal cell conditioned medium (SCM) and stromal cell extract (SCE) on the growth of stromal cells and epithelial cells by [3H]-thymidine incorporation assay. We also examined the expression of mRNAs for aFGF, bFGF, KGF, FGF receptor 1 (FGFR1) and FGFR2 in epithelial and stromal cells using Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) analysis. As the results, both SCM and SCE stimulated the growth of stromal cells, and the growth promoting effects of them to stromal cells were completely suppressed by anti-bFGF neutralizing antibody, but not by anti-aFGF neutralizing antibody at all. SCM also stimulated the growth of epithelial cells. The growth promoting effect of it to epithelial cells was not completely suppressed by anti-bFGF neutralizing antibody, and not by anti-aFGF neutralizing antibody at all. Furthermore, RT-PCR analysis demonstrated the expression of mRNAs for bFGF, KGF and FGFR1 in stromal cells and that of FGFR2 in epithelial cells. These findings suggest that bFGF produced by stromal cells acts on stromal cells through FGFR1 by an autocrine mechanism, KGF produced by stromal cells acts on epithelial cells through FGFR2 by a paracrine manner in human BPH. These mechanisms for the regulation of cell growth by stromal cells were thought to contribute to the development of human BPH.
基质-上皮细胞相互作用对人类良性前列腺增生(BPH)的发展非常重要。前列腺中的生长因子及其受体被认为介导细胞间通讯,并在BPH的发展中发挥一定作用。在众多生长因子中,成纤维细胞生长因子(FGF)家族成员受到的研究最为深入,并且在大鼠或人类前列腺中已鉴定出酸性FGF(aFGF)、碱性FGF(bFGF)和角质形成细胞生长因子(KGF)的mRNA。然而,它们在基质-上皮细胞相互作用中的合成位点和作用仍不明确。在本研究中,为了确定人BPH中基质细胞调节前列腺细胞生长的机制,我们建立了从人BPH组织中分离和培养上皮细胞以及基质细胞的方法。使用这些原代培养的前列腺细胞,我们通过[3H]-胸腺嘧啶核苷掺入试验评估了基质细胞条件培养基(SCM)和基质细胞提取物(SCE)对基质细胞和上皮细胞生长的影响。我们还使用逆转录聚合酶链反应(RT-PCR)分析检测了上皮细胞和基质细胞中aFGF、bFGF、KGF、FGF受体1(FGFR1)和FGFR2的mRNA表达。结果显示,SCM和SCE均刺激了基质细胞的生长,并且它们对基质细胞的生长促进作用被抗bFGF中和抗体完全抑制,但完全不受抗aFGF中和抗体的影响。SCM也刺激了上皮细胞的生长。其对上皮细胞的生长促进作用未被抗bFGF中和抗体完全抑制,也完全不受抗aFGF中和抗体的影响。此外,RT-PCR分析表明基质细胞中存在bFGF、KGF和FGFR1的mRNA表达,上皮细胞中存在FGFR2的mRNA表达。这些发现表明,在人BPH中,基质细胞产生的bFGF通过自分泌机制作用于基质细胞自身的FGFR1,基质细胞产生的KGF通过旁分泌方式作用于上皮细胞的FGFR2。这些基质细胞调节细胞生长的机制被认为有助于人类BPH的发展。