Viard I, Jaillard C, Saez J M
INSERM-INRA U 307, Hôpital Debrousse, Lyon, France.
FEBS Lett. 1993 Aug 9;328(1-2):94-8. doi: 10.1016/0014-5793(93)80972-w.
Nuclear proto-oncoproteins have been implicated in the regulation of gene expression by peptidic hormones and growth factors during cell proliferation and differentiation. In the present study we have investigated in bovine adrenal cells (BAC) the effects of basic fibroblast growth factor (b-FGF), insulin-like growth factor 1 (IGF-I) and transforming growth factor beta (TGF-beta) on c-jun, jun-B and c-fos mRNA levels and on cell growth and differentiation. Factors able to enhance the three proto-oncogenes (IGF-I, b-FGF and angiotensin II (A-II)) stimulate cell growth, whereas those inhibiting cell growth (TGF-beta and ACTH) decrease c-jun mRNA level. These results suggest that expression of c-jun may be required to induce cell proliferation. The relation between proto-oncogenes and the expression of differentiated functions appears to be more complex. Whereas IGF-I, b-FGF and A-II increase the three nuclear proto-oncogenes, the effects of IGF-I and b-FGF on cytochrome P450 17 alpha-hydroxylase mRNA levels are opposite to those of A-II. On the other hand, while TGF-beta and A-II have inhibitory effects on P450 17 alpha mRNA level, they have opposite effects on c-jun mRNA.
核原癌蛋白被认为在细胞增殖和分化过程中参与肽类激素和生长因子对基因表达的调控。在本研究中,我们在牛肾上腺细胞(BAC)中研究了碱性成纤维细胞生长因子(b-FGF)、胰岛素样生长因子1(IGF-I)和转化生长因子β(TGF-β)对c-jun、jun-B和c-fos mRNA水平以及细胞生长和分化的影响。能够增强这三种原癌基因的因子(IGF-I、b-FGF和血管紧张素II(A-II))刺激细胞生长,而那些抑制细胞生长的因子(TGF-β和促肾上腺皮质激素(ACTH))则降低c-jun mRNA水平。这些结果表明,c-jun的表达可能是诱导细胞增殖所必需的。原癌基因与分化功能表达之间的关系似乎更为复杂。虽然IGF-I、b-FGF和A-II增加了这三种核原癌基因,但IGF-I和b-FGF对细胞色素P450 17α-羟化酶mRNA水平的影响与A-II相反。另一方面,虽然TGF-β和A-II对P450 17α mRNA水平有抑制作用,但它们对c-jun mRNA有相反的作用。