安徽农业科学
安徽農業科學
안휘농업과학
JOURNAL OF ANHUI AGRICULTURAL SCIENCES
2010年
7期
3492-3495,3530
,共5页
孙伟%胡亮%赵兴%李官成%付炳方%潘颂华
孫偉%鬍亮%趙興%李官成%付炳方%潘頌華
손위%호량%조흥%리관성%부병방%반송화
小鼠骨髓间充质干细胞%诱导分化%神经细胞
小鼠骨髓間充質榦細胞%誘導分化%神經細胞
소서골수간충질간세포%유도분화%신경세포
rMSCs%Differented%Neuron-like cell
[目的]分离和克隆小鼠骨髓间充质干细胞,并诱导分化为神经元样细胞.[方法]利用Percoll密度梯度离心的方法进行小鼠骨髓间充质干细胞分离及培养,分别采用β-巯基乙醇和BHA诱导分化为神经元样细胞.用神经元特异性烯醇化酶和神经纤维丝蛋白免疫细胞化学方法对已分化的神经元样细胞进行鉴定和分化率分析.[结果]经2种诱导剂诱导的小鼠骨髓间充质干细胞均出现神经元样细胞的分化,胞体呈神经元状,伸出较长轴突样和树突样突起且有分支.而且免疫细胞化学鉴定显示,诱导分化后的神经元样细胞神经元特异性烯醇化酶染色和神经纤维丝蛋白免疫细胞化学染色均呈阳性,β-巯基乙醇诱导分化细胞表达NSE的阳性率为(86.8±2.7)%;诱导分化细胞表达Neurofilament 200 kD的阳性率为(75.2±2.3)%;BHA诱导分化细胞表达NSE的阳性率为(80.5±2.2)%;诱导分化细胞表达Neurofilament 200 kD的阳性率为(73.2±1.6)%.[结论]小鼠骨髓间充质干细胞能够在诱导剂β-巯基乙醇和BNA的诱导下体外诱导分化为神经元样细胞.
[目的]分離和剋隆小鼠骨髓間充質榦細胞,併誘導分化為神經元樣細胞.[方法]利用Percoll密度梯度離心的方法進行小鼠骨髓間充質榦細胞分離及培養,分彆採用β-巰基乙醇和BHA誘導分化為神經元樣細胞.用神經元特異性烯醇化酶和神經纖維絲蛋白免疫細胞化學方法對已分化的神經元樣細胞進行鑒定和分化率分析.[結果]經2種誘導劑誘導的小鼠骨髓間充質榦細胞均齣現神經元樣細胞的分化,胞體呈神經元狀,伸齣較長軸突樣和樹突樣突起且有分支.而且免疫細胞化學鑒定顯示,誘導分化後的神經元樣細胞神經元特異性烯醇化酶染色和神經纖維絲蛋白免疫細胞化學染色均呈暘性,β-巰基乙醇誘導分化細胞錶達NSE的暘性率為(86.8±2.7)%;誘導分化細胞錶達Neurofilament 200 kD的暘性率為(75.2±2.3)%;BHA誘導分化細胞錶達NSE的暘性率為(80.5±2.2)%;誘導分化細胞錶達Neurofilament 200 kD的暘性率為(73.2±1.6)%.[結論]小鼠骨髓間充質榦細胞能夠在誘導劑β-巰基乙醇和BNA的誘導下體外誘導分化為神經元樣細胞.
[목적]분리화극륭소서골수간충질간세포,병유도분화위신경원양세포.[방법]이용Percoll밀도제도리심적방법진행소서골수간충질간세포분리급배양,분별채용β-구기을순화BHA유도분화위신경원양세포.용신경원특이성희순화매화신경섬유사단백면역세포화학방법대이분화적신경원양세포진행감정화분화솔분석.[결과]경2충유도제유도적소서골수간충질간세포균출현신경원양세포적분화,포체정신경원상,신출교장축돌양화수돌양돌기차유분지.이차면역세포화학감정현시,유도분화후적신경원양세포신경원특이성희순화매염색화신경섬유사단백면역세포화학염색균정양성,β-구기을순유도분화세포표체NSE적양성솔위(86.8±2.7)%;유도분화세포표체Neurofilament 200 kD적양성솔위(75.2±2.3)%;BHA유도분화세포표체NSE적양성솔위(80.5±2.2)%;유도분화세포표체Neurofilament 200 kD적양성솔위(73.2±1.6)%.[결론]소서골수간충질간세포능구재유도제β-구기을순화BNA적유도하체외유도분화위신경원양세포.
[Objective]The research compared whole-marrow isolation with density gradient isolation for the purification of rMSCs,and investigated the influence of different culture mediums and serums in culture rMSCs,together with the ability of differenciation into neuron-like cells of rMSCs.[Method]Density gradient isolation combined with adhenerce isolation can purify rMSCs, which was able to differentiate into neuron-like cells and Adipogenic cells, accordingly it provide powerful technical support for the futher study of rMSCs differentiate into neuron like cells.In the research rMSCs (mice barrow mesenchymal stem cells) had been isolated and purified, together with the ability of differenciation into neuron-like cells of rMSCs during cultured with β-Me and BHA. The rate of neuron-like cells induced by β-ME and BHA expressed NSE and NF had also been researched by using the assays of cellular immunity.[Result]The result proved that mouse bone mesenchymal stem cells appeared the morphologic of neuron-like cells after it was induced by β-ME and BHA. The morphology of the cells like the body of neuron cells which were star-like and came to form long branche. It was proved by immunochemist that the neuron-like cells expressed NSE and NF after induced,the rate of neuron-like cells induced by β-ME expressed NSE was (86.8±2.7)%;and the rate of neuron-like cells induced by β-ME expressed Neurofilament 200 kD was (75.2±2.3)%; the rate of neuron-like cells induced by BHA expressed NSE was (80.5±2.2)%;and the rate of neuron-like cells induced by BHA expressed Neurofilament 200 kD was (73.2±1.6)%.[Conclusion]It was proved that mouse mesenchymal stem cells could be differentiated into neuron-like cells in vitro by β-ME or BHA.