Effects of oxygen concentration on the proliferation and differentiation of mouse neural stem cells in vitro

被引:89
作者
Nobutaka Horie [1 ]
Kenji So [2 ]
Takahiro Moriya [1 ]
Naoki Kitagawa [1 ]
Keisuke Tsutsumi [2 ]
Izumi Nagata [2 ]
Kazuyuki Shinohara [2 ]
机构
[1] Department of Neurobiology and Behavior, Unit of Basic Medical Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki 852-8523
[2] Department of Neurosurgery, Nagasaki University Graduate School of Medicine, Nagasaki
关键词
Cerebral ischemia; Differentiation; Hypoxia; Neural stem cell; Proliferation;
D O I
10.1007/s10571-007-9237-y
中图分类号
学科分类号
摘要
Background and purpose: Cerebral ischemia is known to elicit the activation of neural stem cells (NSCs); however its mechanism is not fully determined. Although oxygen concentration is known to mediate many ischemic actions, there has been little attention given to the role of pathological oxygen changes under cerebral ischemia on the activation of NSCs. We investigated the effects of various oxygen concentrations on mouse neural stem cells in vitro. Methods: NSCs were cultured from the ganglionic eminence of fetal ICR mice on embryonic day 15.5 using a neurosphere method. The effects of oxygen concentrations on proliferation, differentiation, and cell death of NSCs were evaluated by bromodeoxyuridine (BrdU) incorporation, immunocytochemistry, and TUNEL assay, respectively. Results: The highest proliferation and the neuronal differentiation of the NSCs were observed in 2% oxygen, which yielded significantly higher proportions of both BrdU-labeled cells and Tuj1-positive cells when compared with 20% and 4% oxygen. On the other hand, the differentiation to the astrocytes was not affected by oxygen concentrations, except in the case of anoxia (0% oxygen). The cell death of the NSCs increased in lower oxygen conditions and peaked at anoxia. Furthermore, the switching of the neuronal subtype differentiation from GABA-positive to glutamate-positive neurons was observed in lower oxygen conditions. Conclusions: These findings raise the possibility that reduced oxygen levels occurring with cerebral ischemia enhance NSC proliferation and neural differentiation, and that mild hypoxia (2% oxygen), which is known to occur in the ischemic penumbra, is suitable for abundant neuronal differentiation. © 2008 Springer Science+Business Media, LLC.
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页码:833 / 845
页数:12
相关论文
共 31 条
[21]  
Pulsinelli W.A., Brierley J.B., Plum F., Temporal profile of neuronal damage in a model of transient forebrain ischemia, Ann Neurol, 11, pp. 491-498, (1982)
[22]  
Reynolds B.A., Tetzlaff W., Weiss S., A multipotent EGF-responsive striatal embryonic progenitor cell produces neurons and astrocytes, J Neurosci, 12, pp. 4565-4574, (1992)
[23]  
Reynolds B.A., Weiss S., Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system, Science, 255, pp. 1707-1710, (1992)
[24]  
Sato K., Hayashi T., Sasaki C., Iwai M., Li F., Manabe Y., Seki T., Abe K., Temporal and spatial differences of PSA-NCAM expression between young-adult and aged rats in normal and ischemic brains, Brain Res, 922, pp. 135-139, (2001)
[25]  
Shingo T., Sorokan S.T., Shimazaki T., Weiss S., Erythropoietin regulates the in vitro and in vivo production of neuronal progenitors by mammalian forebrain neural stem cells, J Neurosci, 21, pp. 9733-9743, (2001)
[26]  
Siesjo B.K., Pathophysiology and treatment of focal cerebral ischemia. Part I: Pathophysiology, J Neurosurg, 77, pp. 169-184, (1992)
[27]  
Smith M.L., Auer R.N., Siesjo B.K., The density and distribution of ischemic brain injury in the rat following 2-10 min of forebrain ischemia, Acta Neuropathol (Berl), 64, pp. 319-332, (1984)
[28]  
Storch A., Paul G., Csete M., Boehm B.O., Carvey P.M., Kupsch A., Schwarz J., Long-term proliferation and dopaminergic differentiation of human mesencephalic neural precursor cells, Exp Neurol, 170, pp. 317-325, (2001)
[29]  
Studer L., Csete M., Lee S.H., Kabbani N., Walikonis J., Wold B., McKay R., Enhanced proliferation, survival, and dopaminergic differentiation of CNS precursors in lowered oxygen, J Neurosci, 20, pp. 7377-7383, (2000)
[30]  
Takagi Y., Nozaki K., Takahashi J., Yodoi J., Ishikawa M., Hashimoto N., Proliferation of neuronal precursor cells in the dentate gyrus is accelerated after transient forebrain ischemia in mice, Brain Res, 831, pp. 283-287, (1999)