中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2013年
7期
1387-1389
,共3页
闫旭%阚世廉%金晔%石忠琪
閆旭%闞世廉%金曄%石忠琪
염욱%감세렴%금엽%석충기
神经细胞%细胞分化%第10号染色体缺失的磷酸酶及张力蛋白同源物基因%雷帕霉素靶蛋白%细胞骨架
神經細胞%細胞分化%第10號染色體缺失的燐痠酶及張力蛋白同源物基因%雷帕黴素靶蛋白%細胞骨架
신경세포%세포분화%제10호염색체결실적린산매급장력단백동원물기인%뢰파매소파단백%세포골가
Nerve cell%Cell differentiation%Phosphatase and tensin homolog deleted in chromosome 10%Mammalian target of rapamycin%Cytoskeleton
目的 观察在体外诱导成人骨髓基质干细胞向神经细胞分化过程中,第10号染色体缺失的磷酸酶及张力蛋白同源物基因(PTEN)/雷帕霉素靶蛋白(mTOR)调节细胞骨架构建的变化特征,并探讨其意义.方法 从成人骨髓中分离基质干细胞,在体外经细胞因子诱导分化2周后成为神经样细胞;应用PTEN抑制剂BPV作用于该细胞,半定量逆转录-聚合酶链反应(RT-PCR)方法研究PTEN下游信号分子mTOR的表达变化;应用结合有荧光剂的鬼笔环肽染色细胞骨架,在荧光显微镜下观察细胞突起内细胞骨架的变化特征及测量细胞突起长度.结果 成人骨髓来源的基质干细胞经诱导分化后,神经细胞特征性标志分子神经元特异性烯醇化酶(NSE)和β-Ⅲ微管蛋白(tubulin)表达水平增加,而神经干细胞的标志物巢蛋白表达先增加后减少(P<0.05);经BPV作用后mTOR的表达水平高于作用前(P<0.05);细胞突起生长的长度从(4.58±1.21) μm增加到(9.09 ±2.68) μm(P <0.05).结论 BMSCs来源的神经细胞分化成熟时,PTEN/mTOR具有调节神经细胞突起内细胞骨架构建的能力.
目的 觀察在體外誘導成人骨髓基質榦細胞嚮神經細胞分化過程中,第10號染色體缺失的燐痠酶及張力蛋白同源物基因(PTEN)/雷帕黴素靶蛋白(mTOR)調節細胞骨架構建的變化特徵,併探討其意義.方法 從成人骨髓中分離基質榦細胞,在體外經細胞因子誘導分化2週後成為神經樣細胞;應用PTEN抑製劑BPV作用于該細胞,半定量逆轉錄-聚閤酶鏈反應(RT-PCR)方法研究PTEN下遊信號分子mTOR的錶達變化;應用結閤有熒光劑的鬼筆環肽染色細胞骨架,在熒光顯微鏡下觀察細胞突起內細胞骨架的變化特徵及測量細胞突起長度.結果 成人骨髓來源的基質榦細胞經誘導分化後,神經細胞特徵性標誌分子神經元特異性烯醇化酶(NSE)和β-Ⅲ微管蛋白(tubulin)錶達水平增加,而神經榦細胞的標誌物巢蛋白錶達先增加後減少(P<0.05);經BPV作用後mTOR的錶達水平高于作用前(P<0.05);細胞突起生長的長度從(4.58±1.21) μm增加到(9.09 ±2.68) μm(P <0.05).結論 BMSCs來源的神經細胞分化成熟時,PTEN/mTOR具有調節神經細胞突起內細胞骨架構建的能力.
목적 관찰재체외유도성인골수기질간세포향신경세포분화과정중,제10호염색체결실적린산매급장력단백동원물기인(PTEN)/뢰파매소파단백(mTOR)조절세포골가구건적변화특정,병탐토기의의.방법 종성인골수중분리기질간세포,재체외경세포인자유도분화2주후성위신경양세포;응용PTEN억제제BPV작용우해세포,반정량역전록-취합매련반응(RT-PCR)방법연구PTEN하유신호분자mTOR적표체변화;응용결합유형광제적귀필배태염색세포골가,재형광현미경하관찰세포돌기내세포골가적변화특정급측량세포돌기장도.결과 성인골수래원적기질간세포경유도분화후,신경세포특정성표지분자신경원특이성희순화매(NSE)화β-Ⅲ미관단백(tubulin)표체수평증가,이신경간세포적표지물소단백표체선증가후감소(P<0.05);경BPV작용후mTOR적표체수평고우작용전(P<0.05);세포돌기생장적장도종(4.58±1.21) μm증가도(9.09 ±2.68) μm(P <0.05).결론 BMSCs래원적신경세포분화성숙시,PTEN/mTOR구유조절신경세포돌기내세포골가구건적능력.
Objective To observe the construction of cytoskeleton modulated by phosphatase and tensin homolog deleted on chromosome ten (PTEN)/mammalian target of rapamycin (mTOR) during the nerve cell differentiation by human bone marrow stem cells in vitro,and to analyze the implication.Methods Adult bone marrow cells were isolated and induced into nerve-like cells by some cytokines in vitro after 2 weeks.The mRNA expression of mTOR which is the downstream molecule of PTEN was compared between un-treated and treated by the BPV (a type of PTEN inhibitor) using semi-quantitative reverse transcriptase-polymerase chain reaction (RT-PCR).The construction patterns of cytoskeleton were indicated by Phalloidin-fluoresceine isothiocyanate (FITC),and observed by the fluorescence microscopy.Results Neuron specific enolase (NSE) and β-Ⅲ tubulin were expressed in these cells after the induction by adult human bone marrow stem cells.nestin,the marker of neural progenitors was expressed increasingly at the beginning,and decreasingly subsequently.The mRNA expression level of mTOR was increased and the lenth of the neurites was from (4.58 ± 1.21) μm to (9.09 ±2.68) μm after the cells were treated by BPV (P < 0.05).Conclusion When the nerve cells derived from bone marrow stem cells obtain the mature differentiation,PTEN/mTOR may possess the the ability of cytoskeleton construction modulation in the neuritis of nerve cells in vitro.