Belmont J W, MacGregor G R, Wager-Smith K, Fletcher F A, Moore K A, Hawkins D, Villalon D, Chang S M, Caskey C T
Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030.
Mol Cell Biol. 1988 Dec;8(12):5116-25. doi: 10.1128/mcb.8.12.5116-5125.1988.
Multiple replication-defective retrovirus vectors were tested for their ability to transfer and express human adenosine deaminase in vitro and in vivo in a mouse bone marrow transplantation model. High-titer virus production was obtained from vectors by using both a retrovirus long terminal repeat promoter and internal transcriptional units with human c-fos and herpes virus thymidine kinase promoters. After infection of primary murine bone marrow with one of these vectors, human adenosine deaminase was detected in 60 to 85% of spleen colony-forming units and in the blood of 14 of 14 syngeneic marrow transplant recipients. This system offers the opportunity to assess methods for increasing efficiency of gene transfer, for regulation of expression of foreign genes in hematopoietic progenitors, and for long-term measurement of the stability of expression in these cells.
在小鼠骨髓移植模型中,对多种复制缺陷型逆转录病毒载体在体外和体内转移并表达人腺苷脱氨酶的能力进行了测试。通过使用逆转录病毒长末端重复启动子以及带有人类c-fos和疱疹病毒胸苷激酶启动子的内部转录单元,从载体中获得了高滴度病毒。用这些载体之一感染原代小鼠骨髓后,在60%至85%的脾集落形成单位以及14只同基因骨髓移植受体中的14只的血液中检测到了人腺苷脱氨酶。该系统为评估提高基因转移效率的方法、调节造血祖细胞中外源基因表达的方法以及长期测量这些细胞中表达稳定性的方法提供了机会。