期刊文献+

小鼠海马发育中Bcl-2和Bax表达的体视学观察

Stereoscopic study on the expression of Bcl-2 and Bax in development of mice hippocampus
下载PDF
导出
摘要 目的探讨B淋巴细胞瘤-2基因(Bcl-2)和促凋亡基因Bax(Bax)在C57/BL6小鼠海马发育过程中的表达变化。方法取胚龄(E)18、20 d和生后(P)1、3、7、14、21、28 d以及2、3、6、15、18个月的C57/BL6小鼠海马,每组8只,应用免疫组织化学技术及体视学方法检测Bcl-2和Bax蛋白的表达。结果 E18 d^P21 d,在齿状回(DG)的颗粒层、海马阿蒙角(CA)以及CA各区(CA1~CA4)的锥体层,Bcl-2和Bax阳性细胞及其体密度均呈现出先逐渐增加再逐渐降低的趋势,除DG区Bax阳性细胞及其体密度在P14 d达到最高外,其他均在P7 d达到最高(P<0.01)。P28 d后均趋于稳定(P>0.05)。CA锥体层及DG颗粒层Bcl-2/Bax的体密度比值在P1d显著降低(P<0.01),之后趋于稳定(P>0.05)。结论小鼠海马Bcl-2和Bax的表达在胚胎发育晚期和生后发育早期较多,而在成年及老年期的表达稳定在较低水平,它们可能参与了海马的塑形过程。 Objective To observe the expression of Bcl-2 and Bax in the development of C57/BL6 mice hippocampus. Methods Mice hippocampus of Embryos (E) 18 day (d), E20 d, postnatal (P) 1 d, P3 d, P7 d, P 14 d, P28 d, P2 month (M), P 3 M, P 6 M, P 15 M, P 18 M were used in this study. Immunohistochemistry and stereoscopy were used to detect the expression of Bcl-2 and Bax protein in the mice hippocampus at different ages. Results From El8 d to P21 d, Bcl-2 and Bax immunoreactive cells in both Ammon' cornu (CA) and dentate gyrus (DG) firstly and gradually increased and then decreased(P 〈 0.01 ). The volume density of both Bcl-2 and Bax immunoreactive cells came to the top on P7 d except the Bax expression in DG which was the highest on P14 d( P 〈 0.01 ). Conclusion The expression of Bcl-2 and Bax is high at the early stage of hippocampus development and then low at its adult stage and senectitude, which may be involved with the forming of hippocampus.
出处 《解剖学报》 CAS CSCD 北大核心 2014年第2期185-189,共5页 Acta Anatomica Sinica
关键词 海马 B淋巴细胞瘤-2基因 促凋亡基因BAX 发育 免疫组织化学 小鼠 Hippocampus B-cell lymphoma-2 Bax Development immunohistochemistry Mouse
  • 相关文献

参考文献14

  • 1Castilla-Ortega E, Pedraza C, Estivill-Torras G, et al. When is adult hippocampal neurogenesis necessary for learning? evidence for animal research [J]. Rev Neurosci, 2011, 22(3) :267-283.
  • 2Vann SD, Albasser MM. Hippoeampus and neocortex: recongnition and spatial memory [ J ]. Curr Opln N eurobiol, 2011, 21 (3) :440- 445.
  • 3Nadler JV. Aspartate release and signaling in the hippocampus [J]. NeurochemRes, 2011, 36(4): 668-676.
  • 4Rodrfguez JJ, Verkhratsky A. Neurogenesis in Alzheimer' s disease [J]. JAnat, 2011, 219(1) :78-89.
  • 5Tellez-Zenteno JF, Wiebe S. Hippocampal stimulation in the treatment of epilepsy [J]. Neurosurg Clin N Am, 2011, 22(4): 465 -475.
  • 6Garcia-Saez AJ. The secrets of the Bcl-2 family[ J]. Cell Death Differ, 2012, 19(11) :1733-1740.
  • 7Waters MJ, Blackmore DG. Growth hormone (GH), brain development and neural stem cells [ J]. Pediatr Endocrinol Rev, 2011, 9(2) :549-553.
  • 8陈燕,秦丽华,陈希平,栾丽菊,王利华.神经调节素对实验性痴呆大鼠的干预作用和可能机制[J].解剖学报,2010,41(5):666-669. 被引量:3
  • 9Colitti M. BCL-2 family of proteins and mammary cellular fate[ J]. Anat Histol Embryol,2012, 41 (4) :237-247.
  • 10Estaquier J, Vallette F, Vayssiere JL, et al. The mitochondrial pathways of apoptosis [ J]. Adv Exp Med Biol, 2012, 942 ( 3 ) : 157-183.

二级参考文献37

  • 1楚晋,李林.脑室灌注β-淀粉样肽致痴呆动物模型[J].中国药理学通报,2004,20(7):827-829. 被引量:24
  • 2王跃春.Y型电迷宫在大鼠学习记忆功能测试中的合理运用[J].中国行为医学科学,2005,14(1):69-70. 被引量:61
  • 3孟艳,王蓉,刘梦霞,盛树力.阿尔茨海默病患者脑神经元凋亡机制中相关因素的研究[J].中华老年医学杂志,2006,25(4):245-247. 被引量:19
  • 4Cotman CW,Anderson AJ.A potential role for apoptosis neurodegeneration and Alzheimer's disease[J].Mol Neurobiol,1995,10 (1):19-21.
  • 5Shimohama S.Apoptosis in Alzheimer's disease-an update[J].Apoptosis,2000,5(1):9-16.
  • 6Li Q,Li Z,Mei YW,et al.Neuregulin attenuated cerebral ischemia-reperfusion injury via inhibiting apoptosis and upregulating aquaporin-4[J].Neurosci Lett,2008,443(3):155-159.
  • 7Nabeshima T.Trial to produce animal model of Alzheimer' s disease by continuous infusion of beta-amyloid protein into the rat cerebral ventricle[J].Nihon Shinkei Seishin Yakurigaku Zasshi,1995,15(5):411-418.
  • 8Viel TA,Caetano AL,Nasello AG,et al.Increases of kinin B1 and B2 receptors binding sites after brain infusion of amyloid-beta 1-40 peptide in rats[J].Neurobio Aging,2008,29(1):1805-1814.
  • 9Tsukamoto E,Hashimoto Y,Kanekura K,et al.Characterization of the toxic mechanism triggered by Alzheimer's amyloid-beta peptides via p75 neurotrophin receptor in neuronal hybrid cells[J].J Neurosci Res,2003,73(5):627-636.
  • 10Abdul HM,Calabrese V,Calvani M,et al.Acetyl-L-carnitine induced up regulation of heat shock proteins protects cortical neurons against amyloid-beta petide 1-42 mediated oxidative stress and neurotoxicity implications for Alzheimer's disease[J].J Neurosci Res,2006,84(2):398-408.

共引文献164

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部