Neural stem cells improve neuronal survival in cultured postmortem brain tissue from aged and Alzheimer patients

被引:28
作者
Wu, L. [1 ,2 ]
Sluiter, A. A. [1 ,2 ]
Guo, Ho-Fu [1 ,2 ]
Balesar, R. A. [3 ]
Swaab, D. F. [3 ]
Zhou, Jiang-Ning [1 ,2 ]
Verwer, R. W. H. [3 ]
机构
[1] Univ Sci & Technol China, Sch Life Sci, Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, Sch Life Sci, Dept Neurobiol, Hefei 230026, Peoples R China
[3] Netherlands Inst Neurosci, Amsterdam, Netherlands
关键词
rat embryonic neural stem cells; neuronal reactivation; tissue culture; Alzheimer's disease;
D O I
10.1111/j.1582-4934.2007.00203.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neurodegenerative diseases are progressive and incurable and are becoming ever more prevalent. To study whether neural stem cell can reactivate or rescue functions of impaired neurons in the human aging and neurodegenerating brain, we co-cultured postmortem slices from Alzheimer patients and control participants with rat embryonic day 14 (E14) neural stem cells. Viability staining based on the exclusion of ethidium bromide by intact plasma membranes showed that there were strikingly more viable cells and fewer dead cells in slices co-cultured with neural stem cells than in untreated slices. The presence of Alzheimer pathology in the brain slices did not influence this effect, although the slices from Alzheimer patients, in general, contained fewer viable cells. Co-culturing with rat E14 fibroblasts did not improve the viability of neurons in the human brain slices. Since the human slices and neural stem cells were separated by a membrane during co-culturing our data show for the first time that neural stem cells release diffusible factors that may improve the survival of aged and degenerating neurons in human brains.
引用
收藏
页码:1611 / 1621
页数:11
相关论文
共 37 条
[1]   Colocalization and fluorescence resonance energy transfer between cdk5 and AT8 suggests a close association in pre-neurofibrillary tangles and neurofibrillary tangles [J].
Augustinack, JC ;
Sanders, JL ;
Tsai, LH ;
Hyman, BT .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2002, 61 (06) :557-564
[2]   Increased proliferation reflects glial and vascular-associated changes, but not neurogenesis in the presenile Alzheimer hippocampus [J].
Boekhoorn, Karin ;
Joels, Marian ;
Lucassen, Paul J. .
NEUROBIOLOGY OF DISEASE, 2006, 24 (01) :1-14
[3]  
Braak H, 1996, ACTA NEUROL SCAND, V93, P3
[4]   Embryonic cortical stem cells secrete diffusible factors to enhance their survival [J].
Chang, MY ;
Park, CH ;
Lee, SH .
NEUROREPORT, 2003, 14 (09) :1191-1195
[5]   Optimization of techniques for the maximal detection and quantification of Alzheimer's-related neuropathology with digital imaging [J].
Cummings, BJ ;
Mason, AJL ;
Kim, RC ;
Sheu, PCY ;
Anderson, AJ .
NEUROBIOLOGY OF AGING, 2002, 23 (02) :161-170
[6]   Neurogenesis in the adult human hippocampus [J].
Eriksson, PS ;
Perfilieva, E ;
Björk-Eriksson, T ;
Alborn, AM ;
Nordborg, C ;
Peterson, DA ;
Gage, FH .
NATURE MEDICINE, 1998, 4 (11) :1313-1317
[7]   A whole brain MR spectroscopy study from patients with Alzheimer's disease and mild cognitive impairment [J].
Falini, A ;
Bozzali, M ;
Magnani, G ;
Pero, G ;
Gambini, A ;
Benedetti, B ;
Mossini, R ;
Franceschi, M ;
Comi, G ;
Scotti, G ;
Filippi, M .
NEUROIMAGE, 2005, 26 (04) :1159-1163
[8]   Tangle and neuron numbers, but not amyloid load, predict cognitive status in Alzheimer's disease [J].
Giannakopoulos, P ;
Herrmann, FR ;
Bussière, T ;
Bouras, C ;
Kövari, E ;
Perl, DP ;
Morrison, JH ;
Gold, G ;
Hof, PR .
NEUROLOGY, 2003, 60 (09) :1495-1500
[9]  
GomezIsla T, 1996, J NEUROSCI, V16, P4491
[10]   Medicine - The amyloid hypothesis of Alzheimer's disease: Progress and problems on the road to therapeutics [J].
Hardy, J ;
Selkoe, DJ .
SCIENCE, 2002, 297 (5580) :353-356