泸州医学院学报
瀘州醫學院學報
로주의학원학보
JOURNAL OF LUZHOU MEDICAL COLLEGE
2015年
1期
32-36
,共5页
邓莉%常能彬%范光碧%高小青%杨朝鲜
鄧莉%常能彬%範光碧%高小青%楊朝鮮
산리%상능빈%범광벽%고소청%양조선
脑出血%骨髓基质干细胞%细胞移植%突触
腦齣血%骨髓基質榦細胞%細胞移植%突觸
뇌출혈%골수기질간세포%세포이식%돌촉
Intracerebral hemorrhage%Bone marrow stromal cells%Cell transplantion%Synaptic
目的::探讨转胶质细胞源性神经营养因子基因的骨髓基质干细胞移植到脑出血大鼠后对其突触可塑性的影响。方法:采用胶原酶诱导大鼠尾壳核出血模型,于建模后第3 d在脑出血部位分别注射生理盐水、BMSCs和GDNF/BMSCs悬液20μl。将48只模型大鼠随机分为生理盐水组、BMSCs组和GDNF/BMSCs组,各组又根据取材时间不同分为1周组和2周组,每亚组8只。通过免疫组织化学与RT-PCR观察出血灶周边突触素Syn和生长相关蛋白GAP-43的蛋白与基因的表达。结果:在1周和2周两个时间点,GDNF/BMSCs组与BMSCs和生理盐水组相比Syn和GAP-43的mRNA以及免疫阳性产物显著增加。结论:GDNF/BMSCs移植较单纯BMSCs更能促进脑出血周边区域神经再生修复。
目的::探討轉膠質細胞源性神經營養因子基因的骨髓基質榦細胞移植到腦齣血大鼠後對其突觸可塑性的影響。方法:採用膠原酶誘導大鼠尾殼覈齣血模型,于建模後第3 d在腦齣血部位分彆註射生理鹽水、BMSCs和GDNF/BMSCs懸液20μl。將48隻模型大鼠隨機分為生理鹽水組、BMSCs組和GDNF/BMSCs組,各組又根據取材時間不同分為1週組和2週組,每亞組8隻。通過免疫組織化學與RT-PCR觀察齣血竈週邊突觸素Syn和生長相關蛋白GAP-43的蛋白與基因的錶達。結果:在1週和2週兩箇時間點,GDNF/BMSCs組與BMSCs和生理鹽水組相比Syn和GAP-43的mRNA以及免疫暘性產物顯著增加。結論:GDNF/BMSCs移植較單純BMSCs更能促進腦齣血週邊區域神經再生脩複。
목적::탐토전효질세포원성신경영양인자기인적골수기질간세포이식도뇌출혈대서후대기돌촉가소성적영향。방법:채용효원매유도대서미각핵출혈모형,우건모후제3 d재뇌출혈부위분별주사생리염수、BMSCs화GDNF/BMSCs현액20μl。장48지모형대서수궤분위생리염수조、BMSCs조화GDNF/BMSCs조,각조우근거취재시간불동분위1주조화2주조,매아조8지。통과면역조직화학여RT-PCR관찰출혈조주변돌촉소Syn화생장상관단백GAP-43적단백여기인적표체。결과:재1주화2주량개시간점,GDNF/BMSCs조여BMSCs화생리염수조상비Syn화GAP-43적mRNA이급면역양성산물현저증가。결론:GDNF/BMSCs이식교단순BMSCs경능촉진뇌출혈주변구역신경재생수복。
Objective:To transplant bone marrow stromal cells (BMSCs) transfected with glial cell line derived neurotrophic factor (GDNF) into rats with intracerebral hemorrhage (ICH) and investigate the effects of GDNF-transfected BMSCs on synaptic plasticity in rats with ICH. Methods: The rat models of ICH were established by injection of collagenase. Forty-eight rats were randomly divided into saline group, BMSCs group and GDNF/BMSCs group. The 20 μl of saline, suspension of BMSCs, GDNF/BMSCs were respectively injected in the three groups at the third day after operation. Each group was subdivided into subgroups of one week and two week according to the sampling time. Immunohistochemistry and RT-PCR were used to detect the expressions of proteins and transcription of genes of Syn and GAP-43 in the margin of ICH. Results: The expression of mRNA and immunoreactive products of Syn and GAP-43 in GDNF/BMSCs group or BMSCs group significantly increased more significanly than that in the saline group sampling at one week and two week respectively. ConclusionTransplantation of BMSCs transfected by GDNF gene promotes neuranagenesis better than pure BMSCs in treatment of ICH.