生物
造血
干细胞
转基因
人口
转导(生物物理学)
遗传增强
表型
绿色荧光蛋白
流式细胞术
维多利亚多管发光水母
基因传递
免疫学
计算生物学
细胞生物学
基因
造血干细胞
诱导多能干细胞
骨髓
融合基因
遗传学
细胞
川地34
血细胞
慢病毒
病毒学
胚胎干细胞
基因表达
作者
Teresa S. Hawley,William G. Telford,Robert G. Hawley
出处
期刊:Stem Cells
[Oxford University Press]
日期:2001-03-01
卷期号:19 (2): 118-124
被引量:33
标识
DOI:10.1634/stemcells.19-2-118
摘要
Hematologic diseases potentially benefiting from gene-based therapies involving hematopoietic stem cells (HSCs) include hereditary hemoglobinopathies, immunodeficiency syndromes, and congenital bleeding disorders such as hemophilia A, as well as acquired diseases like AIDS. Successful treatment of these blood diseases with gene-modified HSCs requires high efficiency gene delivery to the target cell population and persistence of transgene expression following differentiation. We review flow cytometric procedures that permit simultaneous, noninvasive measurements of transgene expression and phenotypic discrimination of hematopoietic cell subsets. Central to this approach has been the recent development of a spectrum of blue, cyan, and yellowish-green fluorescent reporters based on the jellyfish Aequorea victoria green fluorescent protein and the discovery of a red fluorescent protein in DISCOSOMA: coral. This methodology should facilitate the optimization of oncoretroviral and lentiviral vectorology and HSC transduction protocols for the ultimate purpose of HSC-directed gene therapy.
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