Sakurai F, Akitomo K, Kawabata K, Hayakawa T, Mizuguchi H
Laboratory of Gene Transfer and Regulation, National Institute of Biomedical Innovation, Osaka, Japan.
Gene Ther. 2007 Jun;14(11):912-9. doi: 10.1038/sj.gt.3302946. Epub 2007 Mar 22.
Human CD46 (membrane cofactor protein), which serves as a receptor for a variety of pathogens, including strains of measles virus, human herpesvirus type 6 and Neisseria, is rapidly downregulated from the cell surface following infection by these pathogens. Here, we report that replication-incompetent adenovirus (Ad) serotype 35 (Ad35) vectors, which belong to subgroup B and recognize human CD46 as a receptor, downregulate CD46 following infection. A decline in the surface expression of CD46 in human peripheral blood mononuclear cells was detectable 6 h after infection, and reached maximum (72%) 12 h after infection. Ad35 vector-induced downregulation of surface CD46 levels gradually recovered after the removal of Ad35 vectors, however, complete recovery of CD46 expression was not observed even at 96 h after removal. The surface expression of CD46 was also reduced after incubation with fiber-substituted Ad serotype 5 (Ad5) vectors bearing Ad35 fiber proteins, ultraviolet-irradiated Ad35, vectors and recombinant Ad35 fiber knob proteins; in contrast, conventional Ad5 vectors did not induce surface CD46 downregulation, suggesting that the fiber knob protein of Ad35 plays a crucial role in the downregulation of surface CD46 density. These results have important implications for gene therapy using CD46-utilizing Ad vectors and for the pathogenesis of Ads that interact with CD46.
人CD46(膜辅因子蛋白)可作为多种病原体的受体,包括麻疹病毒株、人疱疹病毒6型和奈瑟菌,在被这些病原体感染后,CD46会迅速从细胞表面下调。在此,我们报告,属于B亚组且将人CD46识别为受体的无复制能力腺病毒(Ad)血清型35(Ad35)载体,在感染后会下调CD46。在感染后6小时即可检测到人外周血单核细胞中CD46的表面表达下降,并在感染后12小时达到最大值(72%)。去除Ad35载体后,Ad35载体诱导的表面CD46水平下调逐渐恢复,然而,即使在去除后96小时也未观察到CD46表达完全恢复。用携带Ad35纤维蛋白的纤维替代型Ad血清型5(Ad5)载体、紫外线照射的Ad35载体和重组Ad35纤维结蛋白孵育后,CD46的表面表达也会降低;相比之下,传统的Ad5载体不会诱导表面CD46下调,这表明Ad35的纤维结蛋白在表面CD46密度下调中起关键作用。这些结果对于使用利用CD46的Ad载体进行基因治疗以及与CD46相互作用的Ad的发病机制具有重要意义。