Szaniawska B, Maternicka K, Kowalczyk D, Miłoszewska J, Janik P
Department of Cell Biology, Cancer Center, Warsaw, Poland.
Cancer Lett. 1996 Oct 22;107(2):205-9. doi: 10.1016/0304-3835(96)04369-8.
The invasion/migration of two cell lines, melanoma (MEW) and glioma (BT5C), and their counterparts treated for prolonged time with TPA were studied. On Western blots both cell lines expressed alpha, beta I protein kinase C isoforms, whereas beta II and gamma were not detected. The down-regulation of alpha and beta I PKC was observed in glioma cells after long treatment with TPA, whereas the same treatment of melanoma cells did not lead to PKC downregulation. The down-regulation of PKC was accompanied by stimulation of cell migration/invasion through Transwell chambers coated with collagen IV or fibronectin. In the case of melanoma cells treated with TPA, whose PKC was not down-regulated, the inhibition of migration/invasion was observed. The invasive properties of studied cells did not correlate with any conventional PKC isoform expression.
研究了两种细胞系,即黑色素瘤(MEW)和胶质瘤(BT5C),以及用佛波酯(TPA)长时间处理后的相应细胞系的侵袭/迁移情况。在蛋白质免疫印迹法中,两种细胞系均表达α、βI蛋白激酶C亚型,而未检测到βII和γ亚型。在用TPA长期处理后,胶质瘤细胞中观察到α和βI蛋白激酶C(PKC)的下调,而对黑色素瘤细胞进行相同处理并未导致PKC下调。PKC的下调伴随着通过包被有IV型胶原或纤连蛋白的Transwell小室对细胞迁移/侵袭的刺激。在用TPA处理的黑色素瘤细胞中,其PKC未下调,观察到迁移/侵袭受到抑制。所研究细胞的侵袭特性与任何传统PKC亚型的表达均无相关性。