期刊文献+

移植间充质干细胞在颅脑创伤小鼠小脑的定植与创伤修复 被引量:1

Colonization and Treuma Repair of Transplantated Mesenchymal Stem Cell in Cerebellum of Mouse with Brain Injury
下载PDF
导出
摘要 目的探讨移植间充质干细胞(mesenchymal stem cells,MSCs)在颅脑创伤小鼠小脑的定植及参与创伤修复情况。方法绿色荧光蛋白(green fluorescent protein,GFP)转基因小鼠MSCs的分离培养。制作小鼠颅脑创伤模型后随机分2组,移植组于小鼠颅脑损伤后尾静脉注射分离培养成功的GFP转基因小鼠MSCs;生理盐水组于小鼠脑损伤后尾静脉注射生理盐水。对照组为正常C57BL/6小鼠。免疫组织化学法检测GFP标记MSCs在小鼠小脑的定植情况,并对三组小鼠进行神经行为学和运动功能评分。结果分离培养的GFP标记的MSCs在荧光显微镜下GFP阳性表达。移植组免疫组织化学染色显示在小脑颗粒细胞层边缘和靠近颗粒细胞层部位有阳性的GFP标记MSCs定植。在各时相点,创伤模型小鼠神经行为学和运动功能评分都与对照组有统计学差异(P<0.01)。第14天移植组神经行为学和运动功能评分与对照组比较无统计学差异,在第8天、14天与生理盐水组有统计学差异(P<0.05)。结论移植的MSCs能通过血液系统到达小脑创伤部位定植,并参与小脑功能的恢复。 Objective To explore the colonization and injury repair participation of the transplanted mesenchymal stem cells (MSCs) in the cerebellum of mice with brain injury. Methods MSCs of green fluorescent protein (GFP) trans genie mice were isolated and cultured. Model mice with brain injury were established and randomly divided into transplan tation group and saline group. GFPlabeled MSCs and saline were injected in the caudal vein in transplantation group and saline group respectively. The control group were normal C57BL/6 mice. The expressions of GFPlabeled MSCs were de tected by immunohistochemistry. The neurological behavior and motor function score of the three groups of mice were e valuated. Results The isolated and cultured GFPlabeled MSCs were positively GFP expressed under the fluorescence mi croscope. Transplant 10 days later, immunohistochemical staining showed sitepositive GFPlabeled MSCs colonization in cerebellar granule cell layer edge and near the granule cell layer. At all the timepoints, the model mice with trauma had significantly different neurological behavior and motor function score compared with that of the normal control group (P〈0. 01). , The tranplantation had no difference with the control group at the 14th day, and had significant difference with the control group at the 8th and 14thday (P〉0.05). Conclusion The transplanted MSCs can clolne in the trauma site inthe cerebellum through the blood system and participate in the recovery of cerebellar function.
出处 《华南国防医学杂志》 CAS 2013年第10期707-709,764,共4页 Military Medical Journal of South China
关键词 间充质干细胞 颅脑损伤 移植 Mesenchymal stem cell Traumatic brain injury Transplantation
  • 相关文献

参考文献11

  • 1Hoffman J M, Bell KR, Powell J M,et al. A randomized controlled trial of exercise to improve mood after traumatic brain injury[J]. PMR,2010,2(10):911 -919.
  • 2Gross AK, Norman J, Cook AM. Contemporary pharmacologic is sues in the management, of traumatic brain injury[J ]. J Pharm Pract,2010),23(5) :425 -440.
  • 3Catale C, Germain S, Meulemans T, et al. Exploration of perceptu al and motor inhibition in children with traumatic brain injury[J]. Percept Mot Skills,2011,112(3) :667 -679.
  • 4邓均,艾国平,周桃莉,王军平,徐辉,邹仲敏,董世武,郝磊,冉新泽,粟永萍.G-CSF动员循环间充质干细胞及其对小鼠颅脑损伤修复的可行性分析[J].第三军医大学学报,2007,29(12):1131-1134. 被引量:10
  • 5Bedterson JB, Pitts LH, Tsuji M, et al. Rat middle cerebral artery occluskm: evaluation ot- the model and development of a neurologic examination[J]. Stroke, 1986,17(3) :472-476.
  • 6Shapira Y,Lam AM,Eng CC,et al. Therapeutic time window and dose response of the beneficial effects of ketamine in experimental head injury[J]. Stroke,1994,25(8) : 1637-1643.
  • 7赵红,江城梅,赵文红,申玲,陈丽丽.大豆异黄酮对丙烯酰胺致大鼠小脑损伤的保护作用[J].中国工业医学杂志,2009,22(1):40-41. 被引量:4
  • 8Yoshinaga H, Kobayashi K, Endoh F, et a l. Peculiar involuntary movements in premature babies with specific cerebellar injuries [J]. No To Hattatsu,2012,44(3) :239- 243.
  • 9Rowe RK, Harrison JL, Thomas TC,et al. Using anesthetics andanalgesics in experimental traumatic brain injury[J]. Lab Anita (NY) ,2013,42(8) :286-291.
  • 10Miyamoto K, Ohtaki H, Dohi K, et al. Edaravone increases region- al cerebral blood flow after traumatic brain injury in mice[J]. Acta Neurochir Suppl, 2013,118 : 103-109.

二级参考文献19

共引文献12

同被引文献14

  • 1武强,李露斯,范文辉,宋敏,杨忠.小鼠胚胎神经干细胞海马移植对APP/PS1双转基因AD小鼠的治疗作用[J].第三军医大学学报,2007,29(10):915-918. 被引量:4
  • 2Brian Balin,J. Todd Abrams,John Schrogie.Toward a Unifying Hypothesis in the Development of Alzheimer’s Disease[J]. CNS Neuroscience & Therapeutics . 2011 (6)
  • 3Bloom G S.Amyloid-beta and tau:the trigger and bullet in Alzheimer disease pathogenesis. JAMA Neurol . 2014
  • 4Jisun Lee,Samantha Giordano,Jianhua Zhang.Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling. Biochemical Journal . 2012
  • 5Lu B,Morgans CW,Girman S,Luo J,Zhao J,Du H,Lim S,Ding S,Svendsen C,Zhang K,Wang S.Neural Stem Cells Derived by Small Molecules Preserve Vision. Transl Vis Sci Technol . 2013
  • 6Yonehiro Kanemura.Development of Cell-processing Systems for Human Stem Cells (Neural Stem Cells, Mesenchymal Stem Cells, and iPS Cells) for Regenerative Medicine. The Keio Journal of Medicine . 2010
  • 7Wisniewski T,Goni F.Immunotherapeutic approaches for Alzheimer’’s disease. Neuron . 2015
  • 8Hassan WM,Dostal V,Huemann BN,et al.Identifying Aβ-specific pathogenic mechanisms using a nematode model of Alzheimer’’s disease. Neurobiology of Aging . 2015
  • 9Giaccone G,Orsi L,Cupidi C,et al.Lipofuscin hypothesis of Alzheimer’’s disease. Dement Geriatr Cogn Dis Extra . 2011
  • 10Yang DS,Stavrides P,Saito M,et al.Defective macroautophagic turnover of brain lipids in the Tg CRND8 Alzheimer mouse model:prevention by correcting lysosomal proteolytic deficits. Brain . 2014

引证文献1

二级引证文献3

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