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本文引用的文献

1
Use of Escherichiu coli (E. coli) lacZ (β-Galactosidase) as a Reporter Gene.使用大肠杆菌(E. coli)的lacZ(β-半乳糖苷酶)作为报告基因。
Methods Mol Biol. 1991;7:217-35. doi: 10.1385/0-89603-178-0:217.
2
Gene transfer into neural cells in vitro using adenoviral vectors.利用腺病毒载体在体外将基因导入神经细胞。
Curr Protoc Neurosci. 2001 May;Chapter 4:Unit 4.23. doi: 10.1002/0471142301.ns0423s13.
3
Adenovirus-mediated gene transfer of a secreted transforming growth factor-beta type II receptor inhibits luminal loss and constrictive remodeling after coronary angioplasty and enhances adventitial collagen deposition.腺病毒介导的分泌型转化生长因子β II型受体基因转移可抑制冠状动脉血管成形术后管腔丢失和缩窄性重塑,并增强外膜胶原沉积。
Circulation. 2001 Nov 20;104(21):2595-601. doi: 10.1161/hc4601.099405.
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A genetically modified adenoviral vector exhibits enhanced gene transfer of human smooth muscle cells.
J Vasc Res. 2001 Sep-Oct;38(5):471-8. doi: 10.1159/000051080.
5
Chimeric smooth muscle-specific enhancer/promoters: valuable tools for adenovirus-mediated cardiovascular gene therapy.嵌合型平滑肌特异性增强子/启动子:腺病毒介导的心血管基因治疗的宝贵工具。
Circ Res. 2001 Mar 16;88(5):468-75. doi: 10.1161/01.res.88.5.468.
6
Improved adenovirus vectors for infection of cardiovascular tissues.用于心血管组织感染的改良腺病毒载体。
J Virol. 2001 Apr;75(7):3335-42. doi: 10.1128/JVI.75.7.3335-3342.2001.
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SM22alpha promoter targets gene expression to vascular smooth muscle cells in vitro and in vivo.SM22α启动子在体外和体内将基因表达靶向血管平滑肌细胞。
Mol Med. 2000 Nov;6(11):983-91.
8
Strong promoters are the key to highly efficient, noninflammatory and noncytotoxic adenoviral-mediated transgene delivery into the brain in vivo.强效启动子是在体内将腺病毒介导的转基因高效、无炎症且无细胞毒性地递送至大脑的关键。
Mol Ther. 2000 Oct;2(4):330-8. doi: 10.1006/mthe.2000.0140.
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Transcriptional targeting to anterior pituitary lactotrophic cells using recombinant adenovirus vectors in vitro and in vivo in normal and estrogen/sulpiride-induced hyperplastic anterior pituitaries.
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10
Direct in vivo evidence demonstrating neointimal migration of adventitial fibroblasts after balloon injury of rat carotid arteries.大鼠颈动脉球囊损伤后外膜成纤维细胞向新生内膜迁移的直接体内证据。
Circulation. 2000 Mar 28;101(12):1362-5. doi: 10.1161/01.cir.101.12.1362.

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.

DOI:10.1038/sj.gt.3302044
PMID:12907954
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2902242/
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。