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在腺相关病毒介导下,髓鞘碱性蛋白转录控制区调控下的少突胶质细胞中的基因转移与表达。

Gene transfer and expression in oligodendrocytes under the control of myelin basic protein transcriptional control region mediated by adeno-associated virus.

作者信息

Chen H, McCarty D M, Bruce A T, Suzuki K, Suzuki K

机构信息

Neuroscience Center, University of North Carolina, Chapel Hill, 27599-7525, USA.

出版信息

Gene Ther. 1998 Jan;5(1):50-8. doi: 10.1038/sj.gt.3300547.

Abstract

In this study, a rAAV vector carrying a reporter gene, 'humanized' green fluorescent protein (GFP), linked to the transcriptional control region from the myelin basic protein (MBP) gene (a myelin-forming cell-specific gene) was constructed. Transduction of oligodendrocytes was carried out both in vitro and in vivo. The GFP expression was detected for at least 3 weeks in both transduced oligodendrocyte cell line (MOCH-1 cells) and primary cultures of rat oligodendrocytes. Preferential GFP expression in oligodendrocytes was observed in the primary cultures. In contrast, transduction with rAAV carrying the CMV promoter produced stronger GFP fluorescence in various cell types, with the majority of GFP-expressing cells being the astrocytes. Infusion of approximately 6 x 10(9) particles (2 x 10(5) infectious units) of rAAV-MBP-GFP into mouse brains resulted in the GFP expression specifically in white matter. The GFP protein was detected 15 days later by immunostaining, specifically in the oligodendrocytes. No astrocytes were transduced. Our studies suggested that cell types other than neurons in the central nervous system can also be transduced by rAAV using a cell-type-specific transcriptional control region or promoter. The MBP transcriptional control region might be suitable for gene therapy and other neurobiology studies requiring direct targeting to the myelinating cells.

摘要

在本研究中,构建了一种携带报告基因——与髓鞘碱性蛋白(MBP)基因(一种形成髓鞘细胞特异性基因)转录控制区相连的“人源化”绿色荧光蛋白(GFP)的重组腺相关病毒(rAAV)载体。在体外和体内均对少突胶质细胞进行了转导。在转导的少突胶质细胞系(MOCH - 1细胞)和大鼠少突胶质细胞原代培养物中,GFP表达至少持续检测到3周。在原代培养物中观察到少突胶质细胞中优先表达GFP。相比之下,携带巨细胞病毒(CMV)启动子的rAAV转导在各种细胞类型中产生更强的GFP荧光,大多数表达GFP的细胞是星形胶质细胞。将约6×10⁹个颗粒(2×10⁵个感染单位)的rAAV - MBP - GFP注入小鼠脑内,导致GFP特异性在白质中表达。15天后通过免疫染色检测到GFP蛋白,特异性地在少突胶质细胞中。未转导星形胶质细胞。我们的研究表明,中枢神经系统中除神经元外的其他细胞类型也可通过使用细胞类型特异性转录控制区或启动子的rAAV进行转导。MBP转录控制区可能适用于基因治疗和其他需要直接靶向髓鞘形成细胞的神经生物学研究。

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