Dutton James R, Daughters Randy S, Chen Ying, O'Neill Kathy E, Slack J M W
Stem Cell Institute, University of Minnesota, Minneapolis, Minnesota, USA.
Dev Dyn. 2009 Jun;238(6):1412-21. doi: 10.1002/dvdy.21932.
We show that replication defective adenovirus can be used for localized overexpression of a chosen gene in Xenopus tadpoles. Xenopus contains two homologs of the Coxsackie and Adenovirus Receptor (xCAR1 and 2), both of which can confer sensitivity for adenovirus infection. xCAR1 mRNA is present from the late gastrula stage and xCAR2 throughout development, both being widely expressed in the embryo and tadpole. Consistent with the expression of the receptors, adenovirus will infect a wide range of Xenopus tissues cultured in vitro. It will also infect early embryos when injected into the blastocoel or archenteron cavities. Furthermore, adenovirus can be delivered by localized injection to tadpoles and will infect a patch of cells around the injection site. The expression of green fluorescent protein in infected cells persists for several weeks. This new gene delivery method complements the others that are already available. Developmental Dynamics 238:1412-1421, 2009. (c) 2009 Wiley-Liss, Inc.
我们证明,复制缺陷型腺病毒可用于在非洲爪蟾蝌蚪中局部过表达选定的基因。非洲爪蟾含有柯萨奇病毒和腺病毒受体的两个同源物(xCAR1和2),二者均可赋予对腺病毒感染的敏感性。xCAR1 mRNA从晚期原肠胚阶段开始出现,而xCAR2在整个发育过程中均有表达,二者在胚胎和蝌蚪中均广泛表达。与受体的表达一致,腺病毒可感染多种体外培养的非洲爪蟾组织。当注入囊胚腔或原肠腔时,它也会感染早期胚胎。此外,腺病毒可通过局部注射递送至蝌蚪,并会感染注射部位周围的一片细胞。感染细胞中绿色荧光蛋白的表达可持续数周。这种新的基因递送方法补充了现有的其他方法。《发育动力学》238:1412 - 1421,2009年。(c) 2009威利 - 利斯公司。