Challita P M, Kohn D B
Department of Microbiology, University of Southern California School of Medicine, Los Angeles.
Proc Natl Acad Sci U S A. 1994 Mar 29;91(7):2567-71. doi: 10.1073/pnas.91.7.2567.
We describe studies of gene transfer and expression of the human glucocerebrosidase cDNA by a Moloney murine leukemia virus (MoMuLV)-based retroviral vector in a murine gene transfer/bone marrow transplant (BMT) model. Pluripotent hematopoietic stem cells (HSCs) were assayed as the colony-forming units, spleen (CFU-S) generated after serial transplantation. Transcriptional expression from the MoMuLV long-terminal repeat (LTR) was detected at a high level in the primary (1 degree) CFU-S and tissues of reconstituted BMT recipients. However, we observed transcriptional inactivity of the proviral MoMuLV-LTR in > 90% of the secondary (2 degrees) CFU-S and in 100% of the tertiary (3 degrees) CFU-S examined. We have compared the methylation status of the provirus in the 1 degree CFU-S, which show strong vector expression, to that of the transcriptionally inactive provirus in the 2 degrees and 3 degrees CFU-S by Southern blot analysis using the methylation-sensitive restriction enzyme Sma I. The studies demonstrated a 3- to 4-fold increase in methylation of the Sma I site in the proviral LTR of 2 degrees and 3 degrees CFU-S compared to the transcriptionally active 1 degree CFU-S. These observations may have important implications for future clinical applications of retroviral-mediated gene transfer into HSCs, where persistent gene expression would be needed for an enduring therapeutic effect.
我们描述了在小鼠基因转移/骨髓移植(BMT)模型中,通过基于莫洛尼鼠白血病病毒(MoMuLV)的逆转录病毒载体进行人葡糖脑苷脂酶cDNA基因转移和表达的研究。多能造血干细胞(HSCs)作为连续移植后产生的脾集落形成单位(CFU-S)进行检测。在初次(1°)CFU-S和重建的BMT受体组织中高水平检测到来自MoMuLV长末端重复序列(LTR)的转录表达。然而,我们观察到在超过90%的二次(2°)CFU-S和100%检测的三次(3°)CFU-S中,前病毒MoMuLV-LTR转录无活性。我们通过使用甲基化敏感限制酶Sma I的Southern印迹分析,比较了显示强载体表达的1°CFU-S中前病毒的甲基化状态与2°和3°CFU-S中转录无活性前病毒的甲基化状态。研究表明,与转录活性的1°CFU-S相比,2°和3°CFU-S的前病毒LTR中Sma I位点的甲基化增加了3至4倍。这些观察结果可能对逆转录病毒介导的基因转移到HSCs的未来临床应用具有重要意义,在这种应用中,持久的治疗效果需要持续的基因表达。