Pienimaki J P, Rilla K, Fulop C, Sironen R K, Karvinen S, Pasonen S, Lammi M J, Tammi R, Hascall V C, Tammi M I
Department of Anatomy, University of Kuopio, FIN-70211 Kuopio, Finland.
J Biol Chem. 2001 Jun 8;276(23):20428-35. doi: 10.1074/jbc.M007601200. Epub 2001 Mar 21.
Hyaluronan is an abundant and rapidly turned over matrix molecule between the vital cell layers of the epidermis. In this study, epidermal growth factor (EGF) induced a coat of hyaluronan and a 3-5-fold increase in its rate of synthesis in a rat epidermal keratinocyte cell line that has retained its ability for differentiation. EGF also increased hyaluronan in perinuclear vesicles, suggesting concurrent enhancement in its endocytosis. Cell-associated hyaluronan was most abundant in elongated cells that were stimulated to migrate by EGF, as determined in vitro in a wound healing assay. Large fluctuations in the pool size of UDP-N-acetylglucosamine, the metabolic precursor of hyaluronan, correlated with medium glucose concentrations but not with EGF. Reverse transcriptase-polymerase chain reaction (RT-PCR) showed no increase in hyaluronan synthases 1 and 3 (Has1 and Has3), whereas Has2 mRNA increased 2-3-fold in less than 2 h following the introduction of EGF, as estimated by quantitative RT-PCR with a truncated Has2 mRNA internal standard. The average level of Has2 mRNA increased from approximately 6 copies/cell in cultures before change of fresh medium, up to approximately 54 copies/cell after 6 h in EGF-containing medium. A control medium with 10% serum caused a maximum level of approximately 21 copies/cell at 6 h. The change in the Has2 mRNA levels and the stimulation of hyaluronan synthesis followed a similar temporal pattern, reaching a maximum level at 6 h and declining toward 24 h, a finding in line with a predominantly Has2-dependent hyaluronan synthesis and its transcriptional regulation.
透明质酸是表皮重要细胞层之间一种丰富且快速周转的基质分子。在本研究中,表皮生长因子(EGF)在一种保留了分化能力的大鼠表皮角质形成细胞系中诱导形成一层透明质酸,并使其合成速率提高了3至5倍。EGF还增加了核周囊泡中的透明质酸,表明其胞吞作用同时增强。在伤口愈合试验的体外实验中确定,细胞相关透明质酸在被EGF刺激迁移的细长细胞中最为丰富。透明质酸的代谢前体UDP-N-乙酰葡糖胺的库大小有很大波动,这与培养基中的葡萄糖浓度相关,但与EGF无关。逆转录聚合酶链反应(RT-PCR)显示透明质酸合酶1和3(Has1和Has3)没有增加,而通过使用截短的Has2 mRNA内标进行定量RT-PCR估计,在引入EGF后不到2小时内,Has2 mRNA增加了2至3倍。在更换新鲜培养基之前,培养物中Has2 mRNA的平均水平约为6拷贝/细胞,在含EGF的培养基中培养6小时后,增加到约54拷贝/细胞。含10%血清的对照培养基在6小时时导致的最高水平约为21拷贝/细胞。Has2 mRNA水平的变化和透明质酸合成的刺激遵循相似的时间模式,在6小时达到最高水平,并在24小时时下降,这一发现符合主要依赖Has2的透明质酸合成及其转录调控。