Multipotent stem/progenitor cells with similar properties arise from two neurogenic regions of adult human brain

被引:406
作者
Kukekov, VG
Laywell, ED
Suslov, O
Davies, K
Scheffler, B
Thomas, LB
O'Brien, TF
Kusakabe, M
Steindler, DA
机构
[1] Univ Tennessee, Coll Med, Dept Anat & Neurobiol, Memphis, TN 38163 USA
[2] Univ Tennessee, Coll Med, Dept Neurosurg, Memphis, TN 38163 USA
[3] Methodist Hosp Memphis, Dept Pathol, Memphis, TN 38104 USA
[4] Univ Bonn, Dept Neuropathol, D-5300 Bonn, Germany
[5] RIKEN, Expt Anim Res Lab, Tsukuba, Ibaraki, Japan
基金
美国国家卫生研究院;
关键词
adult human brain; multipotent stem and progenitor cells; neurospheres; neurons and glia; extracellular matrix; developmental genes;
D O I
10.1006/exnr.1999.7028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent in vitro studies have shown that the periventricular subependymal zone (SEZ) of the rodent brain is capable of de novo generation of neurons and glia. There is less information available on neurogenesis in the adult human brain, and no study has shown the clonal generation of neurons and glia from in vitro-generated "neurospheres." Here we describe the isolation of proliferative stem/progenitor cells within neurospheres from two different regions, the SEZ and the hippocampus, from surgical biopsy specimens of adult (24-57 years) human brain. Using light and electron microscopy; immunocytochemistry for a variety of neuronal, glial, and developmental (including extracellular matrix; ECM) markers; and the reverse transcriptase polymerase chain reaction to demonstrate different gene transcripts found in neurospheres, it is shown that the adult human brain harbors a complex population of stem/progenitor cells that can generate neuronal and glial progeny under particular in vitro growth conditions. These methods also show that these neurospheres contain both neurons and glia and demonstrate regional similarities at the mRNA level, indicating common stem/progenitor cell types within two different neurogenic regions of the adult human brain. In addition to the synthesis of developmentally regulated molecules such as the ECM protein tenascin-C, a variety of other genes (e.g., Pax 6) and proteins (e.g., Bcl-2) involved in cell survival and differentiation are expressed by adult human brain neurospheres. (C) 1999 Academic Press.
引用
收藏
页码:333 / 344
页数:12
相关论文
共 79 条
[1]  
Anstrom KK, 1996, DEV DYNAM, V206, P437, DOI 10.1002/(SICI)1097-0177(199608)206:4<437::AID-AJA9>3.0.CO
[2]  
2-J
[3]  
Arsenijevic Y, 1998, J NEUROSCI, V18, P2118
[4]  
Aul C, 1998, HAEMATOLOGICA, V83, P71
[5]  
Bernier PJ, 1998, J NEUROSCI, V18, P2486
[6]   FOCAL BRAIN INJURY AND UP-REGULATION OF A DEVELOPMENTALLY-REGULATED EXTRACELLULAR-MATRIX PROTEIN [J].
BRODKEY, JA ;
LAYWELL, ED ;
OBRIEN, TF ;
FAISSNER, A ;
STEFANSSON, K ;
DORRIES, HU ;
SCHACHNER, M ;
STEINDLER, DA .
JOURNAL OF NEUROSURGERY, 1995, 82 (01) :106-112
[7]   THE COMPLEX NATURE OF INTERACTIVE NEUROREGENERATION-RELATED MOLECULES [J].
BRODKEY, JA ;
GATES, MA ;
LAYWELL, ED ;
STEINDLER, DA .
EXPERIMENTAL NEUROLOGY, 1993, 123 (02) :251-270
[8]   Neuronal progenitors as tools for cell replacement in the nervous system [J].
Brustle, O ;
McKay, RDG .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (05) :688-695
[9]   THE NEUROEPITHELIAL STEM-CELL CONCEPT - IMPLICATIONS FOR NEUROONCOLOGY [J].
BRUSTLE, O ;
MCKAY, RDG .
JOURNAL OF NEURO-ONCOLOGY, 1995, 24 (01) :57-59
[10]   mCD24 expression in the developing mouse brain and in zones of secondary neurogenesis in the adult [J].
Calaora, V ;
Chazal, G ;
Nielsen, PJ ;
Rougon, G ;
Moreau, H .
NEUROSCIENCE, 1996, 73 (02) :581-594