中国医师杂志
中國醫師雜誌
중국의사잡지
JOURNAL OF CHINESE PHYSICIAN
2012年
11期
1451-1454
,共4页
刘俊东%杨进福%汤建华%伍明%史进
劉俊東%楊進福%湯建華%伍明%史進
류준동%양진복%탕건화%오명%사진
骨髓细胞/细胞学%基因表达%间质干细胞/细胞学%反式激活因子类/遗传学%细胞,培养的%转染
骨髓細胞/細胞學%基因錶達%間質榦細胞/細胞學%反式激活因子類/遺傳學%細胞,培養的%轉染
골수세포/세포학%기인표체%간질간세포/세포학%반식격활인자류/유전학%세포,배양적%전염
Bone marrow cells/cytology%Gene expression%Mesenchymal stem cells/cytology%Trans-activators/genetics%Cells,cultured%Transfection
目的 探讨SHH基因转染大鼠骨髓间充质干细胞(MSC)的可行性.方法 利用电转法将SHH基因转染人大鼠骨髓间充质干细胞,在荧光显微镜下观察转染效率;分别绘制未转染及转染SHH基因后细胞生长曲线,观察转染对细胞的影响;采用PCR、RT-PCR、Western-blot检测转染后骨髓间充质干细胞中外源性SHH基因的表达情况.结果 生长曲线显示转染后骨髓间充质干细胞生长曲线指数生长期及平台期延后,在转染后第12天与未转染达到一致.转染后48 h(即将用于移植前),经荧光倒置显微镜观察转染效率为30%,PCR检测转染后骨髓间充质干细胞中SHH表达较未转染细胞明显升高,实时定量PCR检测其升高约7倍左右,通过Western-blot检测转染后SHH蛋白产物表达明显升高.结论 电转法能够有效将外源性SHH基因转染人大鼠MSC并能获得有效表达,为进一步大鼠缺血性心脏病模型的在体基因治疗提供了前提基础.
目的 探討SHH基因轉染大鼠骨髓間充質榦細胞(MSC)的可行性.方法 利用電轉法將SHH基因轉染人大鼠骨髓間充質榦細胞,在熒光顯微鏡下觀察轉染效率;分彆繪製未轉染及轉染SHH基因後細胞生長麯線,觀察轉染對細胞的影響;採用PCR、RT-PCR、Western-blot檢測轉染後骨髓間充質榦細胞中外源性SHH基因的錶達情況.結果 生長麯線顯示轉染後骨髓間充質榦細胞生長麯線指數生長期及平檯期延後,在轉染後第12天與未轉染達到一緻.轉染後48 h(即將用于移植前),經熒光倒置顯微鏡觀察轉染效率為30%,PCR檢測轉染後骨髓間充質榦細胞中SHH錶達較未轉染細胞明顯升高,實時定量PCR檢測其升高約7倍左右,通過Western-blot檢測轉染後SHH蛋白產物錶達明顯升高.結論 電轉法能夠有效將外源性SHH基因轉染人大鼠MSC併能穫得有效錶達,為進一步大鼠缺血性心髒病模型的在體基因治療提供瞭前提基礎.
목적 탐토SHH기인전염대서골수간충질간세포(MSC)적가행성.방법 이용전전법장SHH기인전염인대서골수간충질간세포,재형광현미경하관찰전염효솔;분별회제미전염급전염SHH기인후세포생장곡선,관찰전염대세포적영향;채용PCR、RT-PCR、Western-blot검측전염후골수간충질간세포중외원성SHH기인적표체정황.결과 생장곡선현시전염후골수간충질간세포생장곡선지수생장기급평태기연후,재전염후제12천여미전염체도일치.전염후48 h(즉장용우이식전),경형광도치현미경관찰전염효솔위30%,PCR검측전염후골수간충질간세포중SHH표체교미전염세포명현승고,실시정량PCR검측기승고약7배좌우,통과Western-blot검측전염후SHH단백산물표체명현승고.결론 전전법능구유효장외원성SHH기인전염인대서MSC병능획득유효표체,위진일보대서결혈성심장병모형적재체기인치료제공료전제기출.
Objective To evaluate the feasibility of transfection of Sonic hedgehog gene (SHH)into bone marrow mesenchymal stem cells(BMMSC).Methods After the SHH gene was transfected into BMMSC by electroporation apparatus,the transfection rate was evaluated by fluorescence inverted microscope.The growth curves of untransfected and transfected BMMSC were drawn,respectively,to observe the influence of transfection on cells.The expression of SHH gene in the BMMSC was detected by PCR,RT-PCR,Western-blot analyses.Results Through fluorescence inverted microscope,the observed transfection rate was appropriately 30%,PCR showed a obvious increase of SHH expression in transfected cells than that in untransfected cells,and it is quantified by qPCR for appropriately 7 times.Western-blot further demonstrated that the SHH protein expression in transfected cells had a distinct increase.However,it was observed that the exponential phase of BMMSCSHH growth curve delayed.The growth curves of both overlap 12 days after transfection.Conclusions This electroporation method can transfect exogenous SHH gene into BMMSC sufficiently with the effective protein expression in BMMSCSHH.It is the foundation of further research of genetic therapy for ischemic heart disease.