期刊文献+

神经生长因子对穹窿海马伞切割后海马自体神经干细胞增殖和向神经元分化的影响 被引量:4

THE EFFECTS OF NGF ON THE PROLIFERATION AND DIFFERENTI-ATION OF ENDOGENOUS NSCs IN THE HIPPOCAMPUS INTO NEURONS AFTER FIMBRIA FORNIX TRANSECTION
下载PDF
导出
摘要 目的探讨切割穹窿海马伞及脑室给予神经生长因子(NGF)后,对大鼠海马自体神经干细胞增殖和分化为神经元的影响。方法12只SD大鼠,随机分成给药组和对照组,每组6只,切割右侧穹窿海马伞,两组切割后即时及第2d、4d向侧脑室分别注射NGF和人工脑脊液,并在术后第3~7d每日腹腔注射2次BrdU。于术后28d灌注取脑、冷冻切片,行BrdU/NF-200免疫荧光双标检测。结果海马齿状回内BrdU阳性细胞数,给药组和对照组切割侧明显多于正常侧,给药组切割侧和正常侧分别多于对照组切割侧和正常侧;海马齿状回内的BrdU/NF-200双标神经元数,给药组切割侧最多,给药组正常侧和对照组切割侧较少,而对照组正常侧则无。结论切割穹窿海马伞后,可致大鼠海马齿状回自体神经干细胞增殖加快并向神经元分化,脑室施加NGF可促进其增殖和分化。 Objective To study the effects of fimbria fornix transection and intraventricular injection of nerve growth factor(NGF) on the proliferation and differentiation of endogenous neural stem cells (NSCs)in the hippocampus into neurons. Methods Twelve SD rats were divided into the treatment group and control group randomly, six rats in each group. The right fimbria fornix of rats were transected. NGF and artificial cerebrospinal fluid was injected into the lateral ventricle of rats in the treatment group and control group respectively immediately and on the 2 nd and 4 th day after transection. Bromodeoxyuridin (BrdU) was injected intraperitoneally twice per day from 3 to 7 days after operation. On the 28 th day after operation, the brains were perfused for fixation and frozen section. BrdU/NF-200 double-label immunofluorescence was used to detect the proliferation and differentiation of NSCs into neurons. Results In dentate gyms, the number of BrdU positive cells in the transection side was much more than those of normal side both in the treatment group and the control group, and the BrdU positive cells in treatment group were more than those of control group both in the transection side and normal side; The number of BrdU/NF-200 double labeled neurons was the most in the transection side of the treatment group, less in normal side Gf treatment group and transection side of the control group, but absent in the normal side of the control group. Conclusion Fimbria fornix transection could cause endogenous neural stem cells in the hippocampus proliferate and differentiate into neurons, and intraventricular injection of NGF could facilitate its proliferation and differentiation.
出处 《解剖学报》 CAS CSCD 北大核心 2007年第6期642-646,共5页 Acta Anatomica Sinica
基金 国家自然科学基金资助项目(30670648) 江苏省自然科学基金资助项目(BK2006057)
关键词 神经生长因子 穹窿海马伞切割 海马 神经干细胞 增殖 分化 免疫荧光 大鼠 Nerve growth factor (NGF) Fimbria fornix transection Hippocampus Neural stem cells (NSCs) Proliferation Differentiation Immunofluorescence Rat
  • 相关文献

参考文献16

二级参考文献40

  • 1张新化,金国华,秦建兵,田美玲,黄镇,徐慧君.穹窿海马伞切割侧海马对植入神经干细胞分化为神经元的影响[J].神经解剖学杂志,2004,20(4):360-364. 被引量:28
  • 2陈蓉,金国华,田美玲,朱蕙霞,秦建兵,谭雪锋,徐慧君.海马中56kD蛋白诱导人神经干细胞迁移的作用[J].神经解剖学杂志,2005,21(4):372-376. 被引量:13
  • 3李卫平,姚志彬.老年期痴呆患者脑海马区胆碱能纤维的分布与临床病理研究[J].中华神经精神科杂志,1995,28(2):76-79. 被引量:20
  • 4[5]Renfranz PJ, Cunningham MG, McKay RD. Region-specific differentiation of the hippocampal stem cell line HiB5 upon implantation into the developing mammalian brain. Cell, 1991;66:713-729 被引量:1
  • 5[6]Fishell G. Striatal precursors adopt cortical identities in response to local cues. Development, 1995 ; 121 : 803- 812 被引量:1
  • 6[7]Nishino H, Hida H, Takei N et al. Mesencephalic neural stem (progenitor) cells develop to dopaminergic neurons more strongly in dopamine-depleted striatum than in intact striatum. Exp Neurol, 2000;164:209-214 被引量:1
  • 7[8]Fricker RA, Carpenter MK, Winkler C et al. Site-specific migration and neural differentiation of human neural progenitor cells after transplantation in the adult rat brain. J Neurosci,1999;19:5990~6005 被引量:1
  • 8[12]Tago H, Kimura H, Maeda T. Visualization of detailed acetylcholinesterase fiber and neuron staining in rat brain by a sensitive histochemical procedure. J Histochem Cytochem, 1986;34:1431- 1438 被引量:1
  • 9[1]Reynolds BA, Weiss S. Generation of neurons and astrocytes from isolated cells of the adult mammalian central nervous system. Science, 1992;255:1707-1710 被引量:1
  • 10[2]Meltzer H, Hatton JD, Sang UH. Cell type-specific development of rodent central nervous system progenitor cells in culture. J Neursurg, 1998;88:93-98 被引量:1

共引文献49

同被引文献22

引证文献4

二级引证文献5

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