Erythropoietin promotes hippocampal neurogenesis in in vitro models of neonatal stroke

被引:58
|
作者
Osredkar, Damjan [1 ,4 ]
Sall, Jeffrey W. [2 ]
Bickler, Philip E. [2 ]
Ferriero, Donna M. [1 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Anesthesia & Perioperat Care, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[4] Univ Childrens Hosp, Dept Pediat Neurol, Ljubljana, Slovenia
关键词
Neurogenesis; Hypoxia; Erythropoietin; Hippocampus; Differentiation; Neonate; NEURAL STEM-CELLS; TRANSIENT GLOBAL-ISCHEMIA; FOCAL CEREBRAL-ISCHEMIA; BRAIN-INJURY; SLICE CULTURES; ENHANCED NEUROGENESIS; ADULT NEUROGENESIS; DENTATE GYRUS; RAT; NEURONS;
D O I
10.1016/j.nbd.2010.01.015
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The hippocampus is often injured in neonatal stroke. We have investigated the effect of erythropoietin (EPO) on oxygen-glucose deprived hippocampal slices and hypoxic progenitor cells. EPO improved survival of the organotypic hippocampal slices with significantly less cell death in the dentate gyrus and an increased number of proliferating cells 4-5 days after insult. Significantly fewer markers of neurogenesis were seen after the insult but when EPO was added to the culture medium, neurogenesis was sustained. When hippocampal progenitor cultures were stimulated into differentiation, more cells chose a neuronal cell fate when treated with EPO. These findings support the hypothesis that EPO not only prevents ischemia induced cell death but promotes neuronal cell fate commitment in in vitro models of neonatal stroke. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:259 / 265
页数:7
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