Acsadi G, Jani A, Huard J, Blaschuk K, Massie B, Holland P, Lochmüller H, Karpati G
Montreal Neurological Institute, McGill University, Quebec, Canada.
Gene Ther. 1994 Sep;1(5):338-40.
Human adenovirus (AV) is a favored vector for delivery of therapeutic genes into certain target cells, such as skeletal muscle cells for gene therapy. Here we show that replication-defective (E1 + E3 deleted) human type 5 adenovirus (AV) recombinants containing a reporter gene insert (RSV-luciferase or RSV-Lux) can very efficiently transduce cultured human myoblasts. However, transduction efficiency is about one order of magnitude less in cultured myotubes 16 days postfusion. The high transduction of myoblasts by AV-RSV-Lux could be effectively blocked by an arginine-glycine-asparagine (RGD) oligopeptide that serves as a ligand for the natural internalization receptor of AV. The normalized level of beta 3/beta 5-integrin, the main component of the internalization receptor for AV is about three times as abundant in myoblasts than in myotubes. This could contribute, among other things, to the relatively high susceptibility of myoblasts to AV infection and AV-mediated gene transduction.
人腺病毒(AV)是将治疗性基因导入某些靶细胞(如用于基因治疗的骨骼肌细胞)的理想载体。在此我们表明,含有报告基因插入片段(RSV-荧光素酶或RSV-Lux)的复制缺陷型(E1 + E3缺失)人5型腺病毒(AV)重组体能够非常有效地转导培养的人成肌细胞。然而,在融合后16天的培养肌管中,转导效率约低一个数量级。作为AV天然内化受体配体的精氨酸-甘氨酸-天冬酰胺(RGD)寡肽可有效阻断AV-RSV-Lux对成肌细胞的高效转导。AV内化受体的主要成分β3/β5整合素的标准化水平在成肌细胞中的丰度约为肌管中的三倍。这可能是成肌细胞对AV感染和AV介导的基因转导相对高度敏感的原因之一。