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首页> 外文期刊>Journal of Virological Methods >Specific transduction of HIV-1 envelope expressing cells by retroviral vectors pseudotyped with hybrid CD4/CXCR4 receptors
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Specific transduction of HIV-1 envelope expressing cells by retroviral vectors pseudotyped with hybrid CD4/CXCR4 receptors

机译:通过杂化CD4 / CXCR4受体假型的逆转录病毒载体对HIV-1包膜表达细胞的特异性转导

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Infection of a target cell by HIV is initiated by the interaction of the envelope glycoprotein with the CD4 receptor molecule on the surface of the target cell. This is followed by binding of a coreceptor of the chemokine receptor family and subsequently fusion of viral and cellular membranes. Membrane fusion is independent of whether the viral envelope protein is on the viral or on the cellular membrane. Accordingly, targeting of HIV infected cells by retroviral vectors has been previously achieved both by coincorporation of CD4 and coreceptors into murine leukemia virus (MLV) and lentivirus based vector particles. It was, therefore, tested whether hybrid genes of CD4 and CXCR4 are also able to yield 'receptor' vectors. A construct containing the four extracellular loops of CD4 fused to CXCR4 (CD4-D4-X4) allowed gene transfer into HIV-1 envelope expressing cells by vectors based on either MLV or lentiviruses. The CD4-D2-X4 hybrid receptor, containing the first two extracellular CD4 domains, allowed gene transfer only by lentiviral vectors. Attempts to increase vector titres by deletion of the intracellular part of CXCR4 failed. Vector titres obtained by hybrid receptors were slightly lower than published titres obtained by separate expression of CD4 and CXCR4. Thus, CD4-D4-CXCR4 hybrids are useful for the generation of retroviral and lentiviral vectors with specificity for HIV-1 envelope expressing cells. (C) 2002 Elsevier Science B.V. All rights reserved. [References: 25]
机译:HIV对靶细胞的感染是通过包膜糖蛋白与靶细胞表面上的CD4受体分子相互作用而引发的。随后是趋化因子受体家族的共同受体的结合,随后病毒膜和细胞膜的融合。膜融合与病毒包膜蛋白在病毒膜上还是在细胞膜上无关。因此,先前已经通过将CD4和共受体共同掺入鼠类白血病病毒(MLV)和慢病毒载体颗粒中来实现了逆转录病毒载体对HIV感染细胞的靶向。因此,测试了CD4和CXCR4的杂种基因是否也能够产生“受体”载体。包含与CXCR4融合的四个CD4胞外环的构建体(CD4-D4-X4)允许通过基于MLV或慢病毒的载体将基因转移到HIV-1包膜表达细胞中。包含前两个胞外CD4域的CD4-D2-X4杂合受体仅允许通过慢病毒载体进行基因转移。通过删除CXCR4的细胞内部分来增加载体滴度的尝试失败。通过杂合受体获得的载体滴度略低于通过单独表达CD4和CXCR4获得的公开滴度。因此,CD4-D4-CXCR4杂合体可用于产生对HIV-1包膜表达细胞具有特异性的逆转录病毒和慢病毒载体。 (C)2002 Elsevier Science B.V.保留所有权利。 [参考:25]

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