中华神经医学杂志
中華神經醫學雜誌
중화신경의학잡지
CHINESE JOURNAL OF NEUROMEDICINE
2009年
4期
335-339
,共5页
管玉青%陆兵勋%潘速跃%王晓锋
管玉青%陸兵勛%潘速躍%王曉鋒
관옥청%륙병훈%반속약%왕효봉
大脑中动脉闭塞%骨髓基质细胞%脑缺血%神经功能
大腦中動脈閉塞%骨髓基質細胞%腦缺血%神經功能
대뇌중동맥폐새%골수기질세포%뇌결혈%신경공능
Bone marrow stromal cells%Middle cerebral artery occlusion%Cerebral ischemia%Neurofunction
目的 观察大脑中动脉闭塞(MCAO)模型大鼠脑内移植骨髓基质细胞fBMSCs)的治疗作用,分析植入梗死灶不同区域的BMSCs的存活、迁移情况以及植入细胞的行为与脑内微环境中GFAP阳性细胞的形态关系.方法 75只成年SD大鼠采用随机数字表法分为MCAO组(n=50)和BMSCs移植组(n=25),所有动物均采用线栓法制作MCAO 1 h模型,24 h后BMSCs移植组脑内注射BrdU标记的同种异体BMSCs(2x106个),MCAO组注射等量PBS.MCAO前及MCAO后第1(移植前)、3、5、7、10、14天应用加速转轮试验和贴纸去除试验检测神经功能缺损情况;第14天处死动物,取脑组织切片应用HE染色观察两组的缺血病灶范围,行BrdU和GFAP免疫组化染色观察BMSCs在不同区域和不同胶质细胞环境下的存活和迁移情况.结果 BMSCs移植组MCAO后7 d加速转轮试验结果优于MCAO组,差异有统计学意义(P<0.05);组织学观察发现植入缺血半暗带区的细胞存活数量最多,且向病变方向放射状迁移,植入缺血病灶核心的细胞甚少存活,且无迁移现象.结论 BMSCs脑内移植可改善MCAO后大鼠神经运动功能;活化的星形胶质细胞构成适合植入细胞存活、迁移的环境,而胶质瘢痕阻碍了细胞的迁移.
目的 觀察大腦中動脈閉塞(MCAO)模型大鼠腦內移植骨髓基質細胞fBMSCs)的治療作用,分析植入梗死竈不同區域的BMSCs的存活、遷移情況以及植入細胞的行為與腦內微環境中GFAP暘性細胞的形態關繫.方法 75隻成年SD大鼠採用隨機數字錶法分為MCAO組(n=50)和BMSCs移植組(n=25),所有動物均採用線栓法製作MCAO 1 h模型,24 h後BMSCs移植組腦內註射BrdU標記的同種異體BMSCs(2x106箇),MCAO組註射等量PBS.MCAO前及MCAO後第1(移植前)、3、5、7、10、14天應用加速轉輪試驗和貼紙去除試驗檢測神經功能缺損情況;第14天處死動物,取腦組織切片應用HE染色觀察兩組的缺血病竈範圍,行BrdU和GFAP免疫組化染色觀察BMSCs在不同區域和不同膠質細胞環境下的存活和遷移情況.結果 BMSCs移植組MCAO後7 d加速轉輪試驗結果優于MCAO組,差異有統計學意義(P<0.05);組織學觀察髮現植入缺血半暗帶區的細胞存活數量最多,且嚮病變方嚮放射狀遷移,植入缺血病竈覈心的細胞甚少存活,且無遷移現象.結論 BMSCs腦內移植可改善MCAO後大鼠神經運動功能;活化的星形膠質細胞構成適閤植入細胞存活、遷移的環境,而膠質瘢痕阻礙瞭細胞的遷移.
목적 관찰대뇌중동맥폐새(MCAO)모형대서뇌내이식골수기질세포fBMSCs)적치료작용,분석식입경사조불동구역적BMSCs적존활、천이정황이급식입세포적행위여뇌내미배경중GFAP양성세포적형태관계.방법 75지성년SD대서채용수궤수자표법분위MCAO조(n=50)화BMSCs이식조(n=25),소유동물균채용선전법제작MCAO 1 h모형,24 h후BMSCs이식조뇌내주사BrdU표기적동충이체BMSCs(2x106개),MCAO조주사등량PBS.MCAO전급MCAO후제1(이식전)、3、5、7、10、14천응용가속전륜시험화첩지거제시험검측신경공능결손정황;제14천처사동물,취뇌조직절편응용HE염색관찰량조적결혈병조범위,행BrdU화GFAP면역조화염색관찰BMSCs재불동구역화불동효질세포배경하적존활화천이정황.결과 BMSCs이식조MCAO후7 d가속전륜시험결과우우MCAO조,차이유통계학의의(P<0.05);조직학관찰발현식입결혈반암대구적세포존활수량최다,차향병변방향방사상천이,식입결혈병조핵심적세포심소존활,차무천이현상.결론 BMSCs뇌내이식가개선MCAO후대서신경운동공능;활화적성형효질세포구성괄합식입세포존활、천이적배경,이효질반흔조애료세포적천이.
Objective To observe the therapeutic effect of intraeerebral transplantation of bone marrow stromal ceils(BMSCs)on neurofunctionai recovery after cerebral infarction in rats,and investigate the survival and migration of the transplanted BMSCs in different areas of the ischemic lesion.Methods Seventy-five adult SD rats Were randomly divided into MCAO group(n=50)and BMSCs transplantation group(n=25).All the rats were subjected to middle cerebral artery occlusion(MCAO)by intraluminal filament placement for 1 h,and 24 h after MCAO,the rats in BMSCs transplantation group received iniection of 2x106 rat BMSCs into the ischemia hemisphere.Rotarod and modified adhesive removal tests were performed before and at 1,3,5,7,10and 14 days after MCAO.The rats were sacrificed after the last teSt to measure the sizes of the ischemic lesions and observe the survival and migration of the transplanted BMSCs using BrdU staining and immunohistochemical staining for glial fibrillary acidic protein(GFAP).Results In the rotarod test,significant neurological function recovery Was observed in rats receiving BMSC transplantation 7 days after MCAO in comparison with the rats withoutthe transplantation(P<05).No obvious difference in the lesion sizes was found at 14 days after MCAO between the two groups.In rats receiving BMSCs transplantation,survival and migration of the transplanted BMSCs were identified in different areas of the ischemic lesion.BMSCs injected to the penumbra were found to survive better and preferentially migrate toward the lesion core.Only few BMSCs injected to the lesion core survived and no cell migration Was detected.Large amount of BrdU-positive cells were detected in the areas where activated GFAP-positive cells Were present.The migration of the BMSCs,however,appeared to be limited by the glial sear.Conclusions Intracerebral transplantation of BSMCs Can promote the moor function recovery of the rats after cerebral ischemia.The activated astrocytes provide appropriate environment for the survival of the transplanted BMSCs and allow their migration to the ischemic core,while the glial scar forms an obstacle to the migration of the BMSCs.