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bFGF在局灶性脑缺血后内源性神经干细胞增殖过程中对Id2的影响 被引量:7

Effects of basic fibroblast growth factor on Id2 expression in rat hippocampus neural stem cells after focal cerebral ischemia reperfusion injury
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摘要 目的检测DNA结合抑制物2(inhibitor of DNA binding 2,Id2)在大鼠脑缺血再灌注海马组织神经干细胞中的表达及bFGF的干预作用。探讨影响神经干细胞增殖分化的分子调控机制。方法采用大脑中动脉栓塞(MCAO)制作大鼠脑缺血再灌注模型。用免疫组织化学法检测海马神经干细胞BrdU、Id2的表达及bFGF的干预作用。结果随着脑缺血再灌注第3天缺血海马神经元BrdU阳性细胞明显增多,第7天达高峰,Id2反应产物脑缺血再灌注第3天较正常组增多,随缺血再灌注时间的延长逐渐增多,第7天表达最强,以后表达逐渐减少。注射bFGF后BrdU、Id2的表达明显增加。结论 bFGF促进神经干细胞的增殖及缺血脑组织Id2的表达,提示bFGF促进神经干细胞增殖作用可能由Id2信号介导。 Objective To investigate the effects of basic fibroblast growth factor(bFGF) on Id2 expression and hippocampal neurogenesis in a rat model of cerebral ischemia / reperfusion,explore the related molecular mechanism.Methods The model of transient focal ischemia was made by occlusion of the middle cerebral artery,the expression of BrdU and Id2 and in hippocampus was detected with immunohistochemical method analyzed by microimage system.Results Neural stem cells were activated after cerebral ischemia.After three days,BrdU positive cells in hippocampus were obviously increased.To the seventh day,BrdU positive cells were more than those at any time.The expression of Id2 had similar trend with the expression of BrdU.Following bFGF injection,the expression of hippocampal Id2 had apparently increased in each group.Conclusions bFGF promotes the expression of Id2 in the hippocampus tissue.These findings indicate that bFGF promotion of neural stem cell proliferation may be mediated by Id2 signaling pathway.
出处 《解剖学研究》 CAS 2011年第1期9-12,共4页 Anatomy Research
基金 辽宁省教育厅科学研究计划资助项目(L2010546)
关键词 碱性成纤维细胞生长因子 DNA结合抑制物2 神经干细胞 海马 脑缺血 bFGF Inhibitor of DNA bindingz(Id2) Neural stem cells Hippocampus Cerebral ischemia
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  • 1Luskinm B, Zigova T, Soteres B J, et al. Neuronal progenitor cells derived from the anterior subventricular zone of the neonatal rat forebrain continue to proliferatein vitroand express a neuronal phenotype. Mol Cell Neurosci, 1997,8(5) : 351-366.
  • 2Brock SC, Bonsall J, Luskin MB. The neuronal progenitor cells of the forebrain subventricular zone: intrinsic propertiesin vitro and following transplantation.Methods, 1998,16(3):268-281.
  • 3Luskinm B. Neuroblasts of the postnatalmammalian forebrain: their phenotype and fate. J Neurobiol, 1998, 36(2) : 221-233.
  • 4Norton JD, Deed RW, Cragg SG, et al. Id helix-loophelix proteins in cellgrowth and differentiation. Trends Cell Biol, 1998,8(2) :58-65.
  • 5Norton JD. ID helix-loop-helix proteins in cell growth, differentiation and tumorigenesis. J Cell Sci, 2000,113 (2) : 3897-3905.
  • 6Benezra R, Davis RL, Lockshon D, et al. The protein Id: a negative regulator ofhelix-loop-helix DNA binding proteins. Cell, 1990,61 ( 1 ) :49-59.
  • 7Rockman SP, Currie SA, Ciavarellam O, et al. Id2 is a target of the beta-catenin/T cell factor pathway in colon carcinoma. J Biol Chem, 2001,276 (48) : 45113-45119.
  • 8Ross SE, Greenberg ME, Stiles CD. Basic helix-loophelix factors in cortical development. Neuron, 2003,39 (1):13-25.
  • 9Jen Y, Manova K, Benezrar A. Each member of the Id gene family exhibits a unique expression pattern in mouse gastrulation and neurogenesis. Dev Dyn, 1997, 208 ( 1 ) :92-106.
  • 10Tzeng SF, De-velis J. Idl, Id2, and Id3 gene expression in neural cells during development. Glia, 1998,24(4): 372-381.

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