组织工程与重建外科杂志
組織工程與重建外科雜誌
조직공정여중건외과잡지
JOURNAL OF TISSUE ENGINEERING AND RECONSTRUCTIVE SURGERY
2013年
5期
256-259
,共4页
马迪%严佶祺%彭承宏%施敏敏%陈雪华%王维杰%李宏为
馬迪%嚴佶祺%彭承宏%施敏敏%陳雪華%王維傑%李宏為
마적%엄길기%팽승굉%시민민%진설화%왕유걸%리굉위
人端粒酶逆转录酶%骨髓间充质干细胞%生物学特性%分化潜能
人耑粒酶逆轉錄酶%骨髓間充質榦細胞%生物學特性%分化潛能
인단립매역전록매%골수간충질간세포%생물학특성%분화잠능
Human telomerase reverse transcriptase%Bone marrow mesenchymal stem cells%Biological characteristics%Potential of differentiation
目的将含hTERT基因的重组慢病毒液感染大鼠骨髓间充质干细胞(Bone marrow mesenchymal stem cells, BMSCs),鉴定其生物学特性。方法分别将含hTERT基因重组慢病毒液、空病毒液感染大鼠BMSCs,实验分为MSC-hTERT组、MSC-GFP组和MSC组(未感染组)。体外培养扩增后,通过定量PCR对各组目的基因表达进行检测。观察MSC组及MSC-hTERT组的体外传代次数及细胞形态变化,分析细胞周期。流式细胞仪检测MSC-hTERT组细胞标志物,评估其成骨、成脂分化能力。结果 MSC-hTERT组目的基因mRNA表达均高于另两组,体外培养过程中MSC-hTERT组传代次数和增殖指数高于MSC组,且具备多向分化潜能。结论转染hTERT的BMSCs具备BMSCs同样的生物学特性,且细胞增殖能力加强,可为组织工程研究以及细胞移植治疗提供可靠的种子细胞。
目的將含hTERT基因的重組慢病毒液感染大鼠骨髓間充質榦細胞(Bone marrow mesenchymal stem cells, BMSCs),鑒定其生物學特性。方法分彆將含hTERT基因重組慢病毒液、空病毒液感染大鼠BMSCs,實驗分為MSC-hTERT組、MSC-GFP組和MSC組(未感染組)。體外培養擴增後,通過定量PCR對各組目的基因錶達進行檢測。觀察MSC組及MSC-hTERT組的體外傳代次數及細胞形態變化,分析細胞週期。流式細胞儀檢測MSC-hTERT組細胞標誌物,評估其成骨、成脂分化能力。結果 MSC-hTERT組目的基因mRNA錶達均高于另兩組,體外培養過程中MSC-hTERT組傳代次數和增殖指數高于MSC組,且具備多嚮分化潛能。結論轉染hTERT的BMSCs具備BMSCs同樣的生物學特性,且細胞增殖能力加彊,可為組織工程研究以及細胞移植治療提供可靠的種子細胞。
목적장함hTERT기인적중조만병독액감염대서골수간충질간세포(Bone marrow mesenchymal stem cells, BMSCs),감정기생물학특성。방법분별장함hTERT기인중조만병독액、공병독액감염대서BMSCs,실험분위MSC-hTERT조、MSC-GFP조화MSC조(미감염조)。체외배양확증후,통과정량PCR대각조목적기인표체진행검측。관찰MSC조급MSC-hTERT조적체외전대차수급세포형태변화,분석세포주기。류식세포의검측MSC-hTERT조세포표지물,평고기성골、성지분화능력。결과 MSC-hTERT조목적기인mRNA표체균고우령량조,체외배양과정중MSC-hTERT조전대차수화증식지수고우MSC조,차구비다향분화잠능。결론전염hTERT적BMSCs구비BMSCs동양적생물학특성,차세포증식능력가강,가위조직공정연구이급세포이식치료제공가고적충자세포。
Objective To identify the biological characteristics after infecting the rat BMSCs with recombinant virus supernatant containing hTERT gene. Methods BMSCs were infected with hTERT recombinant virus supernatant (MSC-hTERT group) and empty virus supernatant (MSC-GFP group), the uninfected group (MSC group) was also set up. The expression of target gene was detected by realtime PCR. Number of passages, cell morphology and cell cycle in MSC group and MSC-hTERT group were observed and analyzed. Cell markers of cells in MSC-hTERT group were detected and the potential of differentiation was also evaluated. Results The expression of hTERT was higher in MSC-hTERT group than in the other two groups. Number of passages and proliferation index in MSC-hTERT group were higher than in MSC group. The ability of multi-lineage differentiation potential of cells in MSC-hTERT group was maintained. Conclusion MSCs transfected by hTERT have the same biological characteristics as primary BMSCs and the ability of cell proliferation was strengthened. More cells could be reserved for tissue engineering and cell transplantation therapy.