McAnulty R J, Campa J S, Cambrey A D, Laurent G J
Biochemistry Unit, National Heart and Lung Institute, University of London, U.K.
Biochim Biophys Acta. 1991 Jan 31;1091(2):231-5. doi: 10.1016/0167-4889(91)90066-7.
Transforming growth factor beta (TGF beta) is known to stimulate procollagen production and steady-state levels of procollagen mRNAs, but its ability to affect post-translational processing of procollagen has been little studied. This paper demonstrates the application of recently developed ultrasensitive methods for measuring hydroxyproline to assess rates of procollagen synthesis and degradation in vitro with and without TGF beta. Foetal rat fibroblasts synthesized 8.63 +/- 0.21 pmol hydroxyproline/micrograms DNA per h, which corresponds to approx. 40 molecules of procollagen/cell per s. Addition of TGF beta to cultures increased total amounts of procollagen synthesized and degraded by 112% and 82%, respectively, but there was a significant decrease in the proportion of procollagen degraded (control, 38.0 +/- 1.1%; TGF beta, 32.3 +/- 0.9%; P less than 0.005). This study demonstrates a novel mechanism which may contribute to the TGF beta-induced increase in procollagen production by fibroblasts.
已知转化生长因子β(TGF-β)可刺激前胶原的产生以及前胶原信使核糖核酸的稳态水平,但其对前胶原翻译后加工的影响却鲜有研究。本文展示了最近开发的用于测量羟脯氨酸的超灵敏方法在评估有无TGF-β时体外前胶原合成和降解速率方面的应用。胎鼠成纤维细胞每小时合成8.63±0.21皮摩尔羟脯氨酸/微克DNA,这大约相当于每秒每细胞40个前胶原分子。向培养物中添加TGF-β后,合成和降解的前胶原总量分别增加了112%和82%,但前胶原降解的比例显著下降(对照组为38.0±1.1%;TGF-β组为32.3±0.9%;P<0.005)。本研究证明了一种新机制,该机制可能有助于TGF-β诱导成纤维细胞前胶原产生增加。