Kitchen J R, Cysyk R L
Laboratory of Medicinal Chemistry, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Biochem J. 1995 Jul 15;309 ( Pt 2)(Pt 2):649-56. doi: 10.1042/bj3090649.
Hyaluronic acid (HA) and its synthesis were studied in intact Swiss 3T3 mouse fibroblasts and isolated membranes. HA chains in culture medium, attached to cells and in isolated membranes, were determined to possess average M(r) values of 5.2 x 10(6), 1.8 x 10(6) and 0.14 x 10(6) respectively. Log cells were determined to possess 680,000 HA molecules/cell, and to release 120,000 HA chains/h. The time required for intact cells to synthesize and release a complete HA chain was approximately 4 h, with elongation proceeding at a rate of 57 dimers/min. The amount of cell-associated HA of various cell populations correlated strongly with their rate of HA release into culture media and with the HA synthetase activity determined for their membranes. Prevention of protein synthesis with cycloheximide decreased the rate of HA synthesis of log cells and HA synthetase activity of isolated membranes by 50% within 2-3 h. Because of the similarity between the biological lifetime of HA synthetase and the time required to synthesize a HA chain, we propose a model where each synthetase makes only one HA chain; after synthesis of a complete HA chain, HA synthetase activity is terminated as its HA chain is released from the cell.
在完整的瑞士3T3小鼠成纤维细胞和分离的细胞膜中研究了透明质酸(HA)及其合成过程。测定了培养基中、附着于细胞上以及分离细胞膜中的HA链,其平均分子量(M(r))值分别为5.2×10⁶、1.8×10⁶和0.14×10⁶。对数期细胞被测定为每个细胞拥有680,000个HA分子,并以每小时释放120,000条HA链的速度释放。完整细胞合成并释放一条完整HA链所需的时间约为4小时,延伸速度为每分钟57个二聚体。不同细胞群体中与细胞相关的HA量与其向培养基中释放HA的速度以及测定的其细胞膜的HA合成酶活性密切相关。用环己酰亚胺抑制蛋白质合成在2 - 3小时内使对数期细胞的HA合成速度和分离细胞膜的HA合成酶活性降低了50%。由于HA合成酶的生物学寿命与合成一条HA链所需的时间相似,我们提出了一个模型,即每个合成酶仅合成一条HA链;在合成一条完整的HA链后,随着其HA链从细胞中释放,HA合成酶活性终止。