Promoter-targeted selection and isolation of neural progenitor cells from the adult human ventricular zone

被引:19
作者
Roy, NS
Benraiss, A
Wang, S
Fraser, RAR
Goodman, R
Couldwell, WT
Nedergaard, M
Kawaguchi, A
Okano, H
Goldman, SA
机构
[1] Cornell Univ, Med Ctr, Dept Neurol & Neurosci, New York, NY 10021 USA
[2] Cornell Univ, Dept Neurosurg, Coll Med, New York, NY 10021 USA
[3] Columbia Univ Coll Phys & Surg, Dept Neurosurg, New York, NY 10032 USA
[4] New York Med Coll, Dept Neurosurg, Valhalla, NY 10595 USA
[5] New York Med Coll, Dept Cell Biol, Valhalla, NY 10595 USA
[6] Osaka Univ, Div Neonatol, Grad Sch Med, Osaka, Japan
[7] Japan Sci & Technol Corp, Suita, Osaka, Japan
关键词
neurogenesis; precursor cells; stem cells; promoters; subependyma;
D O I
10.1002/(SICI)1097-4547(20000201)59:3<321::AID-JNR5>3.0.CO;2-9
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Adult humans, like their nonhuman mammalian counterparts, harbor persistent neural progenitor cells in the forebrain ventricular lining. In the absence of adequate surface markers, however, these cells have proven difficult to isolate for study. We have previously identified and selected neural progenitor cells from both the fetal and adult rodent ventricular zone (VZ), by sorting forebrain cells transfected with plasmid DNA encoding the gene for green fluorescent protein driven by the early neuronal promoter for T alpha 1 tubulin (P/T alpha 1:hGFP). We have now extended this approach by purifying both P/T alpha 1:hGFP tubulin-defined neuronal progenitors, as well as potentially less committed E/nestin:hGFP-defined neural progenitor cells, from the adult human VZ. The ventricular wall of the temporal horn of the lateral ventricle was dissected from temporal lobes obtained from four adult patients undergoing therapeutic lobectomy. These samples were dissociated, and the cultured cells transduced with either PT alpha 1:hGFP or E/nestin:EGFP plasmid DNA. A week later, the cells were redissociated, selected via fluorescence-activated cell sorting (FACS) on the basis of neural promoter-driven GFP expression, and replated. The majority of these cells expressed the early neuronal protein beta III-tubulin upon FAGS; within the week thereafter, most matured as morphologically evident neurons that coexpressed beta III-tubulin and microtubule-associated protein (MAP)-2. Many of these neurons had incorporated bromodeoxyuridine in vitro in the days before FAGS, indicating their mitogenesis in vitro. Thus, the use of fluorescent transgenes under the control of early neural promoters permits the enrichment of neuronal progenitor cells from the adult human ventricular zone. The specific acquisition, in both purity and number, of residual neural progenitor cells from the adult human brain may now permit hitherto unfeasible studies of both their biology and practical application. (C) 2000 Wiley-Liss, Inc.
引用
收藏
页码:321 / 331
页数:11
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