中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2014年
19期
3030-3035
,共6页
张恩丰%曹锐%徐韬%王晓燕%买尔旦·买买提%王国旗%盛伟斌
張恩豐%曹銳%徐韜%王曉燕%買爾旦·買買提%王國旂%盛偉斌
장은봉%조예%서도%왕효연%매이단·매매제%왕국기%성위빈
干细胞%脂肪干细胞%脂肪间充质干细胞%不同代次%细胞培养%细胞分化%神经球%国家自然科学基金
榦細胞%脂肪榦細胞%脂肪間充質榦細胞%不同代次%細胞培養%細胞分化%神經毬%國傢自然科學基金
간세포%지방간세포%지방간충질간세포%불동대차%세포배양%세포분화%신경구%국가자연과학기금
stem cels%mesenchymal stem cels%neural stem cels%neurons
背景:脂肪间充质干细胞是一组具有多向分化潜能的干细胞,体外在一定条件下可分化为神经干细胞。目的:观察不同代次大鼠脂肪间充质干细胞体外培养增殖能力及诱导成神经球的潜力。<br> 方法:取SD大鼠脂肪体外分离培养出脂肪间充质干细胞并传代扩增,分别在P3、P6、P10、P20时观察其形态学变化、测定增殖速度。流式细胞仪检测定不同代次细胞表型及细胞周期。将脂肪间充质干细胞诱导为神经球,计数成神经球率。<br> 结果与结论:脂肪间充质干细胞主要呈长梭形,不同代次的脂肪间充质干细胞均具有很强的体外增殖能力;除P3细胞其他代次细胞均高表达CD29、CD44、CD73,低表达CD45、CD34。细胞周期中G0/G1期细胞所占比例P3为93.4%、P6为92.7%、P10为92.4%、P20为86.0%。P6、P10诱导成神经球率均显著高于P20(P<0.05),P3细胞较难诱导成神经球。提示以脂肪间充质干细胞作为种子细胞时,应注意选择适宜的扩增代数,以便在获得足够纯度细胞的同时保留细胞最佳的分化潜力。
揹景:脂肪間充質榦細胞是一組具有多嚮分化潛能的榦細胞,體外在一定條件下可分化為神經榦細胞。目的:觀察不同代次大鼠脂肪間充質榦細胞體外培養增殖能力及誘導成神經毬的潛力。<br> 方法:取SD大鼠脂肪體外分離培養齣脂肪間充質榦細胞併傳代擴增,分彆在P3、P6、P10、P20時觀察其形態學變化、測定增殖速度。流式細胞儀檢測定不同代次細胞錶型及細胞週期。將脂肪間充質榦細胞誘導為神經毬,計數成神經毬率。<br> 結果與結論:脂肪間充質榦細胞主要呈長梭形,不同代次的脂肪間充質榦細胞均具有很彊的體外增殖能力;除P3細胞其他代次細胞均高錶達CD29、CD44、CD73,低錶達CD45、CD34。細胞週期中G0/G1期細胞所佔比例P3為93.4%、P6為92.7%、P10為92.4%、P20為86.0%。P6、P10誘導成神經毬率均顯著高于P20(P<0.05),P3細胞較難誘導成神經毬。提示以脂肪間充質榦細胞作為種子細胞時,應註意選擇適宜的擴增代數,以便在穫得足夠純度細胞的同時保留細胞最佳的分化潛力。
배경:지방간충질간세포시일조구유다향분화잠능적간세포,체외재일정조건하가분화위신경간세포。목적:관찰불동대차대서지방간충질간세포체외배양증식능력급유도성신경구적잠력。<br> 방법:취SD대서지방체외분리배양출지방간충질간세포병전대확증,분별재P3、P6、P10、P20시관찰기형태학변화、측정증식속도。류식세포의검측정불동대차세포표형급세포주기。장지방간충질간세포유도위신경구,계수성신경구솔。<br> 결과여결론:지방간충질간세포주요정장사형,불동대차적지방간충질간세포균구유흔강적체외증식능력;제P3세포기타대차세포균고표체CD29、CD44、CD73,저표체CD45、CD34。세포주기중G0/G1기세포소점비례P3위93.4%、P6위92.7%、P10위92.4%、P20위86.0%。P6、P10유도성신경구솔균현저고우P20(P<0.05),P3세포교난유도성신경구。제시이지방간충질간세포작위충자세포시,응주의선택괄의적확증대수,이편재획득족구순도세포적동시보류세포최가적분화잠력。
BACKGROUND:Adipose-derived mesenchymal stem cels are a group of pluripotent stem cels, and under certain conditions can differentiate into neural stem celsin vitro. <br> OBJECTIVE:To investigate the proliferative and differentiation ability of different passage mesenchymal stem cellfrom adipose tissue into neurospheres. <br> METHODS:The adipose-derived mesenchymal stem cels from Sprague-Dawley rats were separated and culturedin vitro, and morphology and proliferation rate of cels were observed and compared respectively at passages 3, 6, 10 and 20. The cellsurface antigens and cels cycle were identified by flow cytometry. Furthermore, adipose-derived mesenchymal stem cels were induced into neurospheres, and the neurosphere rate was counted. <br> RESULTS AND CONCLUSION: Adipose-derived mesenchymal stem cels were mainly in long spindle shape, and cels at different passages had highly proliferative capacity in vitro. Except passage 3, adipose-derived mesenchymal stem cels strongly expressed CD29, CD44, CD73 and lowly expressed CD45 and CD34. The proportion of G0/G1 phase in cellcycle was 93.4% at passage 3, 92.7% at passage 6, 92.4% at passage 10, 86.0% at passage 20. Adipose-derived mesenchymal stem cels at passages 6 and 10 were easier to differentiate into neurospheres than those at passage 20 (P < 0.05), but cels at passage 3 were difficult to differentiate into neurospheres. Therefore, when using adipose-derived mesenchymal stem cels as seed cels, we should pay attention to choose the appropriate amplification passage in order to obtain the cels with best differentiation potential and cellpurity.