Yeowell H N, Walker L C, Marshall M K, Murad S, Pinnell S R
Division of Dermatology, Duke University Medical Center, Durham, North Carolina 27710, USA.
Arch Biochem Biophys. 1995 Aug 20;321(2):510-6. doi: 10.1006/abbi.1995.1424.
Lysyl hydroxylase (LH) catalyzes the formation of hydroxylysine required for the intermolecular cross-linking of collagen, which is an essential step in collagen biosynthesis. Dermal fibroblasts from patients with Ehlers-Danlos Syndrome type VI (EDS VI), an inherited connective tissue disorder, express decreased levels of LH activity. In the present study we have shown that both the mRNA and the enzyme activity of LH in skin fibroblasts from one EDS VI patient (AT750), a compound heterozygote for the LH gene, are increased by administration of ascorbate and hydralazine, either individually or in combination. Although the AT750 cells express only 24% of the LH activity found in normal cells, a similar fold increase in activities in both EDS VI and normal cells was observed following treatment with ascorbate (1.5- to 2-fold) and hydralazine (2- to 4-fold), which paralleled the increase in their steady state LH mRNAs. Ascorbate increased total collagen production by 2-fold from a similar basal level of collagen synthesis in each cell type. This was confirmed by protein gel analysis which showed increases in pro alpha 1(I), pro alpha 2(I), and pro alpha 1(III) collagen chains in both normal and EDS VI cells. This ascorbate-mediated increase of alpha 1(I) collagen resulted from increased mRNAs for alpha 1(I) collagen in both cell types. Hydralazine treatment, with or without ascorbate, severely decreased the alpha 1(I) collagen mRNAs in fibroblasts from both AT750 and the normal donor; total collagen synthesis was similarly reduced. This study shows that LH activity, which is severely deficient in fibroblasts from an EDS VI patient, can be upregulated by administration of ascorbate and hydralazine as a result of the increased mRNA for LH, suggesting that the mechanism for the regulation of the LH gene is functioning normally in this patient.
赖氨酰羟化酶(LH)催化胶原蛋白分子间交联所需的羟赖氨酸的形成,这是胶原蛋白生物合成中的关键步骤。患有遗传性结缔组织疾病——Ⅵ型埃勒斯-当洛综合征(EDS VI)的患者的真皮成纤维细胞中,LH活性水平降低。在本研究中,我们发现,对于一名LH基因复合杂合子的EDS VI患者(AT750),单独或联合给予抗坏血酸和肼苯哒嗪后,其皮肤成纤维细胞中LH的mRNA和酶活性均有所增加。尽管AT750细胞的LH活性仅为正常细胞的24%,但在用抗坏血酸(1.5至2倍)和肼苯哒嗪(2至4倍)处理后,EDS VI细胞和正常细胞的活性均出现了相似倍数的增加,这与它们的LH稳态mRNA的增加情况平行。抗坏血酸使每种细胞类型中相似的基础胶原蛋白合成水平的总胶原蛋白产量增加了2倍。蛋白质凝胶分析证实了这一点,该分析显示正常细胞和EDS VI细胞中的α1(I)前胶原、α2(I)前胶原和α1(III)前胶原链均有所增加。这种抗坏血酸介导的α1(I)胶原蛋白增加是由于两种细胞类型中α1(I)胶原蛋白的mRNA增加所致。无论是否使用抗坏血酸,肼苯哒嗪处理均会严重降低AT750和正常供体的成纤维细胞中α1(I)胶原蛋白的mRNA;总胶原蛋白合成也同样减少。本研究表明,一名EDS VI患者的成纤维细胞中严重缺乏的LH活性,可通过给予抗坏血酸和肼苯哒嗪上调,这是由于LH的mRNA增加,提示该患者中LH基因的调控机制正常运作。