Sisson J C, Castor C W, Klavons J A
J Lab Clin Med. 1980 Aug;96(2):189-97.
Human synovial fibroblasts synthesize hyaluronic acid, a process that can be stimulated by a number of agents. Several steps in the synthetic pathway could be the locus at which these stimulators act; the final step, promoted by hyaluronic acid synthetase, was selectd for study. Hyaluronic acid synthetase is an enzyme system that transfers monosaccharide units to nascent hyaluronic acid chains. Activities of the enzyme were determined in lysates of cultured synovial fibroblasts by measuring incorporation of 14C-UDP-glucuronic acid into hyaluronic acid. Rates of hyaluronic acid synthesis were increased by adding CTAP-I or CTAP-III, DbcAMP, or prostaglandin E2 to the cultures. In each instance, hyaluronic acid synthetase activity was enhanced in a manner comparable to that seen in hyaluronic acid synthesis. The changes in enzyme and product were observed as early as 6 hr after cultures were exposed to CTAP-III, and both indices declined when this stimulator was withdrawn for 24 hr. Although DbcAMP incrased the hyaluronic acid synthetase activity of intact fibroblasts, it had no effect on the enzyme in lysates of cells. In the cultured cells, cycloheximide reduced basal levels of synthetase activity and hyaluronic acid synthesis of hyaluronic acid may do so by inducing hyaluronic acid synthetase.
人滑膜成纤维细胞合成透明质酸,这一过程可被多种因子刺激。合成途径中的几个步骤可能是这些刺激物作用的位点;由透明质酸合成酶促进的最后一步被选作研究对象。透明质酸合成酶是一种将单糖单位转移至新生透明质酸链的酶系统。通过测量14C-UDP-葡萄糖醛酸掺入透明质酸的量,在培养的滑膜成纤维细胞裂解物中测定该酶的活性。向培养物中添加CTAP-I或CTAP-III、二丁酰环磷腺苷(DbcAMP)或前列腺素E2可提高透明质酸的合成速率。在每种情况下,透明质酸合成酶活性均以与透明质酸合成中所见类似的方式增强。早在培养物暴露于CTAP-III后6小时就观察到酶和产物的变化,当撤去该刺激物24小时后,这两个指标均下降。尽管DbcAMP增加了完整成纤维细胞的透明质酸合成酶活性,但对细胞裂解物中的该酶没有影响。在培养细胞中,环己酰亚胺降低了合成酶活性的基础水平,透明质酸的合成可能是通过诱导透明质酸合成酶来实现的。