Tajima S, Wachi H, Hayashi A
Department of Dermatology, School of Medicine, Keio University, Tokyo, Japan.
Keio J Med. 1995 Dec;44(4):140-5. doi: 10.2302/kjm.44.140.
Treatment of cultured smooth muscle cells with ascorbic acid resulted in an accumulation of tropoelastin in the culture medium in dose-dependent and exposure time-dependent manner under the condition in which collagen synthesis was stimulated 2-fold. The steady-state level of elastin mRNA was essentially unchanged, whereas collagen mRNA content increased 2-fold by ascorbic acid treatment. Newly synthesized tropoelastin was hydroxylated in the presence of ascorbic acid but was underhydroxylated in a scorbutic condition. Short pulse experiments showed that the secretion rate of tropoelastin was unaltered by ascorbic acid treatment. Pulse-chase experiment demonstrated that the level of fully hydroxylated tropoelastin in the medium of ascorbate-treated cells was greater than that of under-hydroxylated tropoelastin. These results indicate that accumulation of tropoelastin in the medium by ascorbic acid is related to an increased stability of hydroxylated tropoelastin and/or its impaired incorporation into insoluble elastin.
在胶原蛋白合成被刺激两倍的条件下,用抗坏血酸处理培养的平滑肌细胞,会导致原弹性蛋白以剂量和暴露时间依赖的方式在培养基中积累。弹性蛋白mRNA的稳态水平基本不变,而抗坏血酸处理使胶原蛋白mRNA含量增加了两倍。新合成的原弹性蛋白在抗坏血酸存在的情况下发生羟基化,但在坏血病条件下羟基化不足。短脉冲实验表明,抗坏血酸处理不会改变原弹性蛋白的分泌速率。脉冲追踪实验证明,抗坏血酸处理细胞的培养基中完全羟基化的原弹性蛋白水平高于羟基化不足的原弹性蛋白水平。这些结果表明,抗坏血酸使原弹性蛋白在培养基中积累与羟基化原弹性蛋白稳定性增加和/或其掺入不溶性弹性蛋白受损有关。