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一种新型的启动子和增强子组合在腺病毒介导的基因转移后,可在体外增加血管平滑肌细胞中的转基因表达,并在体内增加冠状动脉中的转基因表达。

A novel combination of promoter and enhancers increases transgene expression in vascular smooth muscle cells in vitro and coronary arteries in vivo after adenovirus-mediated gene transfer.

作者信息

Appleby C E, Kingston P A, David A, Gerdes C A, Umaña P, Castro M G, Lowenstein P R, Heagerty A M

机构信息

Vascular Gene Therapy Unit, Manchester, UK.

出版信息

Gene Ther. 2003 Sep;10(18):1616-22. doi: 10.1038/sj.gt.3302044.

Abstract

Recombinant adenoviruses are employed widely for vascular gene transfer. Vascular smooth muscle cells (SMCs) are a relatively poor target for transgene expression after adenovirus-mediated gene delivery, however, even when expression is regulated by powerful, constitutive viral promoters. The major immediate-early murine cytomegalovirus enhancer/promoter (MIEmCMV) elicits substantially greater transgene expression than the human cytomegalovirus promoter (MIEhCMV) in all cell types in which they have been compared. The Woodchuck hepatitis virus post-transcriptional regulatory element (WPRE) increases transgene expression in numerous cell lines, and fragments of the smooth muscle myosin heavy chain (SMMHC) promoter increase expression within SMC from heterologous promoters. We therefore, compared the expression of beta-galactosidase after adenovirus-mediated gene transfer of lacZ under the transcriptional regulation of a variety of combinations of the promoters and enhancers described, in vitro and in porcine coronary arteries. We demonstrate that inclusion of WPRE and a fragment of the rabbit SMMHC promoter along with MIEmCMV increases beta-galactosidase expression 90-fold in SMC in vitro and approximately 40-fold in coronary arteries, compared with vectors in which expression is regulated by MIEhCMV alone. Expression cassette modification represents a simple method of improving adenovirus-mediated vascular gene transfer efficiency and has important implications for the development of efficient cardiovascular gene therapy strategies.

摘要

重组腺病毒被广泛用于血管基因转移。然而,即使转基因表达受强大的组成型病毒启动子调控,在腺病毒介导的基因传递后,血管平滑肌细胞(SMC)仍是转基因表达相对较差的靶细胞。在所有已比较的细胞类型中,主要立即早期小鼠巨细胞病毒增强子/启动子(MIEmCMV)引发的转基因表达比人巨细胞病毒启动子(MIEhCMV)显著更高。土拨鼠肝炎病毒转录后调控元件(WPRE)可增加许多细胞系中的转基因表达,平滑肌肌球蛋白重链(SMMHC)启动子片段可增加异源启动子在SMC内的表达。因此,我们在体外和猪冠状动脉中比较了在上述各种启动子和增强子组合的转录调控下,腺病毒介导的lacZ基因转移后β-半乳糖苷酶的表达。我们证明,与仅由MIEhCMV调控表达的载体相比,包含WPRE和兔SMMHC启动子片段以及MIEmCMV可使体外SMC中的β-半乳糖苷酶表达增加90倍,并使冠状动脉中的表达增加约40倍。表达盒修饰是提高腺病毒介导的血管基因转移效率的一种简单方法,对高效心血管基因治疗策略的发展具有重要意义。

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