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作 者:潘德顺[1] 于江洲[1] 郝天玲[1] 王迪浔[1]
出 处:《中国病理生理杂志》1998年第6期608-611,共4页Chinese Journal of Pathophysiology
基 金:国家自然科学基金
摘 要:目的和方法:体外合成红细胞生成素(Epo)3′-增强子野生型及突变型片段,借助脂质体,转入内皮细胞,用半定量RT-PCR方法测定分离细胞在常氧或缺氧条件下培养4h的环加氧酶2(COX-2)mRNA。结果:(1)大鼠主动脉内皮细胞、肺微血管内皮细胞在常氧下培养,有COX-2基因表达;(2)缺氧能诱导这两种细胞COX-2基因表达增加;(3)野生型Epo3′-增强子片段能阻断缺氧对内皮细胞COX-2基因表达的诱导作用,而突变片段则无此作用。结论:在COX-2基因序列中,可能存在Epo3′-端增强子片段。AIM and METHODS:Wild and mutant Epo 3'-enchancer DNA fragments were synthesized in vitro . Cultured endothelial cells were transfected by wild or mutant fragments. Total RNA was extracted from endothelial cells exposed to normoxia or hypoxia for 4h. The amount of COX-2 mRNA was measured by semiquantitative RT-PCR. RESULTS:1. There was expression of COX-2 gene in both aortic endothelial cells and pulmonary vascular endothelial cells in normoxia. 2. Hypoxia increased COX-2 gene expression in these two kinds of endothelial cells. 3. The wild Epo 3'-enchaner fragments inhibited the hypoxia-induced expression of COX-2 gene, whereas the mutant sequence did not. CONCLUSION:The increase of COX-2 expression in hypoxia might result from the combination of activated hypoxia inducible factor -1 with Epo 3'-enhancer-like sequence in COX-2 gene.
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