Herz J, Gerard R D
Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas 75235.
Proc Natl Acad Sci U S A. 1993 Apr 1;90(7):2812-6. doi: 10.1073/pnas.90.7.2812.
We have explored the use of adenovirus-mediated gene transfer to transiently elicit production of low density lipoprotein (LDL) receptors in mice. A recombinant adenovirus carrying the human LDL receptor cDNA restored LDL receptor function in receptor-deficient cultured cells. Intravenous injection of recombinant virus acutely lowered plasma cholesterol levels and increased the rate of 125I-labeled LDL clearance from the circulation in normal mice. At 4 days after virus injection, the t1/2 of plasma LDL was reduced up to 10-fold. An estimated 90% of the parenchymal cells in liver expressed the adenovirus-transferred genes as judged by immunofluorescence of LDL receptors or by beta-galactosidase staining. These results demonstrate that adenovirus-mediated transfer of the LDL receptor gene provides an efficient way of augmenting LDL receptor gene function in the liver over the short term.
我们已经探索了利用腺病毒介导的基因转移来短暂诱导小鼠产生低密度脂蛋白(LDL)受体。携带人LDL受体cDNA的重组腺病毒可恢复受体缺陷培养细胞中的LDL受体功能。静脉注射重组病毒可迅速降低正常小鼠的血浆胆固醇水平,并提高循环中125I标记的LDL清除率。在病毒注射后4天,血浆LDL的半衰期缩短至原来的十分之一。通过LDL受体免疫荧光或β-半乳糖苷酶染色判断,估计肝脏中90%的实质细胞表达了腺病毒转移的基因。这些结果表明,腺病毒介导的LDL受体基因转移提供了一种在短期内增强肝脏中LDL受体基因功能的有效方法。