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
41期
6573-6577
,共5页
刘德胜%肖诗亮%王博%周诚
劉德勝%肖詩亮%王博%週誠
류덕성%초시량%왕박%주성
干细胞%骨髓干细胞%胸腺素β4%骨髓间充质干细胞%基因%凋亡%Bax%Bcl-2
榦細胞%骨髓榦細胞%胸腺素β4%骨髓間充質榦細胞%基因%凋亡%Bax%Bcl-2
간세포%골수간세포%흉선소β4%골수간충질간세포%기인%조망%Bax%Bcl-2
stem cells%mesenchymal stem cells%thymosin%apoptosis
背景:研究表明体外培养细胞加入胸腺素β4能增加细胞的抗凋亡能力,若在缺氧环境中上调胸腺素β4基因在骨髓间充干细胞中的表达,其抗凋亡能力如何改变,目前鲜见报道。<br> 目的:观察胸腺素β4基因修饰的骨髓间充质干细胞在缺氧环境中的凋亡率改变,并探讨其是否通过调控Bax、Bcl-2表达影响凋亡能力。<br> 方法:将携带有胸腺素β4基因的慢病毒转染骨髓间充质干细胞,转染完毕后利用Western blot法检测胸腺素β4在骨髓间充质干细胞中的表达。将细胞分为胸腺素β4转染组、对照病毒组、未转染组,分别置于缺氧环境中。流式细胞仪检测3组细胞凋亡率;Western blot法检测3组细胞中Bax和Bcl-2蛋白表达情况。<br> 结果与结论:Western blot检测结果示,胸腺素β4基因在骨髓间充质干细胞中成功表达。流式细胞仪结果示,胸腺素β4转染组细胞凋亡率较对照病毒组、未转染组低,而对照病毒组、未转染组凋亡率差异无显著性意义。Western blot结果显示,Bcl-2蛋白在胸腺素β4转染组中表达量较对照病毒组、未转染组高,Bax蛋白在胸腺素β4转染组表达量较对照病毒组、未转染组低,而对照病毒组、未转染组中Bax、Bcl-2表达差异无显著性意义。提示过表达胸腺素β4基因可增加骨髓间充质干细胞在缺氧环境中的抗凋亡能力,其可能的作用机制是调控Bax和Bcl-2蛋白表达水平。
揹景:研究錶明體外培養細胞加入胸腺素β4能增加細胞的抗凋亡能力,若在缺氧環境中上調胸腺素β4基因在骨髓間充榦細胞中的錶達,其抗凋亡能力如何改變,目前鮮見報道。<br> 目的:觀察胸腺素β4基因脩飾的骨髓間充質榦細胞在缺氧環境中的凋亡率改變,併探討其是否通過調控Bax、Bcl-2錶達影響凋亡能力。<br> 方法:將攜帶有胸腺素β4基因的慢病毒轉染骨髓間充質榦細胞,轉染完畢後利用Western blot法檢測胸腺素β4在骨髓間充質榦細胞中的錶達。將細胞分為胸腺素β4轉染組、對照病毒組、未轉染組,分彆置于缺氧環境中。流式細胞儀檢測3組細胞凋亡率;Western blot法檢測3組細胞中Bax和Bcl-2蛋白錶達情況。<br> 結果與結論:Western blot檢測結果示,胸腺素β4基因在骨髓間充質榦細胞中成功錶達。流式細胞儀結果示,胸腺素β4轉染組細胞凋亡率較對照病毒組、未轉染組低,而對照病毒組、未轉染組凋亡率差異無顯著性意義。Western blot結果顯示,Bcl-2蛋白在胸腺素β4轉染組中錶達量較對照病毒組、未轉染組高,Bax蛋白在胸腺素β4轉染組錶達量較對照病毒組、未轉染組低,而對照病毒組、未轉染組中Bax、Bcl-2錶達差異無顯著性意義。提示過錶達胸腺素β4基因可增加骨髓間充質榦細胞在缺氧環境中的抗凋亡能力,其可能的作用機製是調控Bax和Bcl-2蛋白錶達水平。
배경:연구표명체외배양세포가입흉선소β4능증가세포적항조망능력,약재결양배경중상조흉선소β4기인재골수간충간세포중적표체,기항조망능력여하개변,목전선견보도。<br> 목적:관찰흉선소β4기인수식적골수간충질간세포재결양배경중적조망솔개변,병탐토기시부통과조공Bax、Bcl-2표체영향조망능력。<br> 방법:장휴대유흉선소β4기인적만병독전염골수간충질간세포,전염완필후이용Western blot법검측흉선소β4재골수간충질간세포중적표체。장세포분위흉선소β4전염조、대조병독조、미전염조,분별치우결양배경중。류식세포의검측3조세포조망솔;Western blot법검측3조세포중Bax화Bcl-2단백표체정황。<br> 결과여결론:Western blot검측결과시,흉선소β4기인재골수간충질간세포중성공표체。류식세포의결과시,흉선소β4전염조세포조망솔교대조병독조、미전염조저,이대조병독조、미전염조조망솔차이무현저성의의。Western blot결과현시,Bcl-2단백재흉선소β4전염조중표체량교대조병독조、미전염조고,Bax단백재흉선소β4전염조표체량교대조병독조、미전염조저,이대조병독조、미전염조중Bax、Bcl-2표체차이무현저성의의。제시과표체흉선소β4기인가증가골수간충질간세포재결양배경중적항조망능력,기가능적작용궤제시조공Bax화Bcl-2단백표체수평。
BACKGROUND:Studies have shown that thymosinβ4 can improve the anti-apoptotic ability of a variety of cells, but the reports describing the changes in the anti-apoptotic ability of bone mesenchymal stem cells modified with thymosinβ4 gene in the hypoxic environment are rare. <br> OBJECTIVE:To observe the change in the apoptotic rate of bone mesenchymal stem cells modified with thymosinβ4 gene in the hypoxic environment, and to explore whether thymosinβ4 affects the apoptosis of bone marrow mesenchymal stem cells via regulating the expression of Bax and Bcl-2. <br> METHODS:Bone marrow mesenchymal stem cells were transfected with the recombinant lentiviral vector over-expressing the thymosinβ4 gene, and then we observed the expression of thymosinβ4 using western blot assay. cells were divided into three groups:thymosinβ4 transfection group, control virus group, and untreated group. Al three groups were placed in a hypoxic environment. The apoptotic rate of bone marrow mesenchymal stem cells was evaluated by the flow cytometry assay. The expression of Bax and Bcl-2 protein was detected by western blot. <br> RESULTS AND CONCLUSION:Thymosinβ4 gene was expressed successful y in the bone marrow mesenchymal stem cells showed by the western blot. The apoptotic rate of bone marrow mesenchymal stem cells in the hypoxic environment was lower in the thymosinβ4 transfection group than the control virus group and untreated group;while there was no difference between the latter two groups. Western blot results showed that the expression of Bcl-2 protein was higher in the thymosinβ4 transfection group than the control virus group and untreated group, and the expression of Bax protein was lower in the thymosinβ4 transfection group than the control virus group and untreated group. No difference in the expression of Bax and Bcl-2 was found between the control virus group and untreated group. These findings indicate that thymosinβ4 overexpression can improve the anti-apoptotic ability of bone mesenchymal stem cells modified in the hypoxic environment, and its possible mechanism is through regulating the expression of Bax and Bcl-2 protein.