Hofbauer Karl-Heinz, Gess Bernhard, Lohaus Christiane, Meyer Helmut E, Katschinski Dörte, Kurtz Armin
Institut für Physiologie der Universität Regensburg, Germany.
Eur J Biochem. 2003 Nov;270(22):4515-22. doi: 10.1046/j.1432-1033.2003.03846.x.
In this study, we have characterized the influence of hypoxia on the expression of hydroxylases crucially involved in collagen fiber formation, such as prolyl-4-hydroxylases (Ph4) and procollagen lysyl-hydroxylases (PLOD). Using the rat vascular smooth muscle cell line A7r5, we found that an hypoxic atmosphere caused a characteristic time-dependent five- to 12-fold up-regulation of the mRNAs of the two P4h alpha-subunits [alphaI (P4ha1) and alphaII (P4ha2)] and of two lysylhydroxylases (PLOD1 and PLOD2). These effects of hypoxia were mimicked by the iron-chelator deferoxamine (100 micro m) and by cobaltous chloride (100 micro m). The hypoxic induction of these genes was also seen in the mouse juxtaglomerular As4.1 cell line and mouse hepatoma cell line Hepa1 but was almost absent in the mutant cell line Hepa1C4, which is defective for the hypoxia-inducible transcription factor 1 (HIF-1). In addition, the enzyme expression was induced by hypoxia in mouse embryonic fibroblasts but not in embryonic fibroblasts lacking the HIF-1alpha subunit. These findings indicate that hypoxia stimulates the gene expression of a cluster of hydroxylases that are indispensible for collagen fiber formation. Strong indirect evidence, moreover, suggests that the expression of these enzymes during hypoxia is coordinated by HIF-1.
在本研究中,我们已明确了缺氧对胶原纤维形成中关键的羟化酶表达的影响,这些羟化酶包括脯氨酰 - 4 - 羟化酶(Ph4)和前胶原赖氨酰羟化酶(PLOD)。利用大鼠血管平滑肌细胞系A7r5,我们发现缺氧环境会导致两种P4hα亚基[αI(P4ha1)和αII(P4ha2)]以及两种赖氨酰羟化酶(PLOD1和PLOD2)的mRNA出现特征性的、随时间变化的5至12倍上调。缺氧的这些效应可被铁螯合剂去铁胺(100 μM)和氯化钴(100 μM)模拟。在小鼠肾小球旁As4.1细胞系和小鼠肝癌细胞系Hepa1中也观察到了这些基因的缺氧诱导现象,但在缺氧诱导转录因子1(HIF - 1)存在缺陷的突变细胞系Hepa1C4中几乎未出现这种现象。此外,缺氧可诱导小鼠胚胎成纤维细胞中的酶表达,但在缺乏HIF - 1α亚基的胚胎成纤维细胞中则不会。这些发现表明,缺氧会刺激对胶原纤维形成不可或缺的一组羟化酶的基因表达。此外,有力的间接证据表明,缺氧期间这些酶的表达是由HIF - 1协调的。