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造血过程的模拟:对溶酶体酶紊乱基因治疗的启示。

Simulation of hematopoiesis: implications for the gene therapy of lysosomal enzyme disorders.

作者信息

Abkowitz J L, Persik M T, Catlin S N, Guttorp P

机构信息

Department of Medicine, University of Washington, Seattle, 98195 (USA).

出版信息

Acta Haematol. 1996;95(3-4):213-7. doi: 10.1159/000203880.

Abstract

Although the hematopoietic stem cell is an attractive target for gene transfer, little is known about its biology in vivo in large animals (including humans). We have studied the in vivo behavior of hematopoietic stem cells in glucose-6-phosphate dehydrogenase heterozygous (female Safari) cats, and demonstrated that clonal instability persists for up to 4.5 years after autologous marrow transplantation. This contrasts with the 2-6 months of clonal disequilibrium reported in comparable murine studies. Our data also suggest that hematopoietic stem cells do not self-renew more than once every 3 weeks. These data may have relevance for strategies to optimize gene therapy in large animals and, by extension, in humans.

摘要

尽管造血干细胞是基因转移的一个有吸引力的靶点,但对于其在大型动物(包括人类)体内的生物学特性却知之甚少。我们研究了葡萄糖-6-磷酸脱氢酶杂合(雌性萨法里)猫体内造血干细胞的行为,并证明自体骨髓移植后克隆不稳定性持续长达4.5年。这与在类似小鼠研究中报道的2-6个月的克隆不平衡形成对比。我们的数据还表明,造血干细胞每3周不会自我更新超过一次。这些数据可能与优化大型动物基因治疗策略相关,进而与人类基因治疗策略相关。

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