Narayanan A S, Page R C
Biochem Biophys Res Commun. 1987 Jun 15;145(2):639-45. doi: 10.1016/0006-291x(87)91012-6.
The mechanism by which serum stimulates collagen production by fibroblasts was examined. Fibroblasts were exposed to various concentrations of serum and collagen production and mRNA levels were measured. Collagen production was determined as collagenase digestible radioactivity and collagen mRNA levels were measured using a [35S]UTP-labelled pro alpha 1[I] probe. The results showed that increased collagen production correlated with enhanced mRNA levels. Extra- and intracellular collagen degradation was similar in control and serum treated cultures, and "G1" and "S" phase fibroblasts contained similar levels of collagen mRNA. We conclude that serum regulation of collagen synthesis occurs primarily at the transcriptional level and that activation of collagen synthesis is not coupled to mitogenic stimulation.
研究了血清刺激成纤维细胞产生胶原蛋白的机制。将成纤维细胞暴露于不同浓度的血清中,并测量胶原蛋白的产生量和mRNA水平。胶原蛋白的产生量通过胶原酶可消化放射性来测定,胶原蛋白mRNA水平则使用[35S]UTP标记的前α1[I]探针进行测量。结果表明,胶原蛋白产生量的增加与mRNA水平的提高相关。在对照培养物和血清处理的培养物中,细胞外和细胞内的胶原蛋白降解情况相似,并且“G1”期和“S”期的成纤维细胞所含的胶原蛋白mRNA水平相似。我们得出结论,血清对胶原蛋白合成的调节主要发生在转录水平,并且胶原蛋白合成的激活与有丝分裂刺激无关。