Ultrasound-targeted microbubble destruction improves the low density lipoprotein receptor gene expression in HepG2 cells

被引:47
作者
Guo, DP
Li, XY
Sun, P
Tang, YB
Chen, XY
Chen, Q
Fan, LM [1 ]
Zang, B
Shao, LZ
Li, XR
机构
[1] Nanjing Med Univ, Inst Reprod Med, Nanjing 210029, Peoples R China
[2] Nanjing Med Univ, Atherosclerosis Res Ctr, Nanjing 210029, Peoples R China
[3] Nanjing Med Univ, Prov Lab Human Funct Genom, Nanjing 210029, Peoples R China
[4] Wuxi No 1 Hosp, Div Cardiovasc, Wuxi 214002, Peoples R China
基金
中国国家自然科学基金;
关键词
microbubble; ultrasound; transfection; LDLR; gene therapy;
D O I
10.1016/j.bbrc.2006.02.179
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ultrasound-targeted microbubble destruction had been employed in gene delivery and promised great potential. Liver has unique features that make it attractive for gene therapy. However, it poses formidable obstacles to hepatocyte-specific gene delivery. This study was designed to test the efficiency of therapeutic gene transfer and expression mediated by ultrasound/rnicrobubble strategy in HepG(2) cell line. Air-filled albumin microbubbles were prepared and mixed with plasmid DNA encoding low density lipoprotein receptor (LDLR) and green fluorescent protein. The mixture of the DNA and microbubbles was administer to cultured HepG(2) cells under variable ultrasound conditions. Transfection rate of the transferred gene and cell viability were assessed by FACS analysis, confocal laser scanning microscopy, Western blot analysis and Trypan blue staining. The result demonstrated that microbubbles with ultrasound irradiation can significantly elevate exogenous LDLR gene expression and the expressed LDLRs were functional and active to uptake their ligands. We conclude that ultrasound-targeted microbubble destruction has the potential to promote safe and efficient LDLR gene transfer into hepatocytes. With further refinement, it may represent an effective nonviral avenue of gene therapy for liver-involved genetic diseases. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:470 / 474
页数:5
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