解剖学杂志
解剖學雜誌
해부학잡지
CHINESE JOURNAL OF ANATOMY
2015年
3期
284-287
,共4页
孙尧%何玉兰%于晓龙%程燕%宋博毅
孫堯%何玉蘭%于曉龍%程燕%宋博毅
손요%하옥란%우효룡%정연%송박의
血管化%组织工程%间充质干细胞
血管化%組織工程%間充質榦細胞
혈관화%조직공정%간충질간세포
vascularization%tissue engineering%marrow mesenchymal stem cells
目的::探讨体外构建血管化组织工程心肌的可行性。方法:大鼠骨髓间充质干细胞以浓度为10μmol/L 的5-氮胞苷诱导为心肌细胞并用 DAPI 标记、骨髓源内皮祖细胞以内皮细胞培养基 EGM2-MV 定向诱导为内皮细胞并用 CM-dil 标记。标记后的心肌细胞与内皮祖细胞按2∶1比例,以4×106个/ml 的密度种植于 Matrigel 基质胶支架上。同种密度心肌细胞种植为对照组。对复合体形态、细胞分布等进行观察。结果:H-E 染色及荧光显微镜观察可见两组复合体的细胞分布均匀,生长状态良好;单纯心肌细胞种植组可见细胞黏附聚集生长,并未出现网状结构,而2∶1混合培养组24 h 后可见内皮细胞相互连接成网状结构,出现典型的“成血管现象”,且形成的血管样结构明显多于对照组;心肌细胞凋亡数较对照组少。结论:骨髓源性心肌细胞与骨髓源性内皮细胞联合种植于 Matrigel 基质胶共培养,可于体外成功构建血管化组织工程心肌。
目的::探討體外構建血管化組織工程心肌的可行性。方法:大鼠骨髓間充質榦細胞以濃度為10μmol/L 的5-氮胞苷誘導為心肌細胞併用 DAPI 標記、骨髓源內皮祖細胞以內皮細胞培養基 EGM2-MV 定嚮誘導為內皮細胞併用 CM-dil 標記。標記後的心肌細胞與內皮祖細胞按2∶1比例,以4×106箇/ml 的密度種植于 Matrigel 基質膠支架上。同種密度心肌細胞種植為對照組。對複閤體形態、細胞分佈等進行觀察。結果:H-E 染色及熒光顯微鏡觀察可見兩組複閤體的細胞分佈均勻,生長狀態良好;單純心肌細胞種植組可見細胞黏附聚集生長,併未齣現網狀結構,而2∶1混閤培養組24 h 後可見內皮細胞相互連接成網狀結構,齣現典型的“成血管現象”,且形成的血管樣結構明顯多于對照組;心肌細胞凋亡數較對照組少。結論:骨髓源性心肌細胞與骨髓源性內皮細胞聯閤種植于 Matrigel 基質膠共培養,可于體外成功構建血管化組織工程心肌。
목적::탐토체외구건혈관화조직공정심기적가행성。방법:대서골수간충질간세포이농도위10μmol/L 적5-담포감유도위심기세포병용 DAPI 표기、골수원내피조세포이내피세포배양기 EGM2-MV 정향유도위내피세포병용 CM-dil 표기。표기후적심기세포여내피조세포안2∶1비례,이4×106개/ml 적밀도충식우 Matrigel 기질효지가상。동충밀도심기세포충식위대조조。대복합체형태、세포분포등진행관찰。결과:H-E 염색급형광현미경관찰가견량조복합체적세포분포균균,생장상태량호;단순심기세포충식조가견세포점부취집생장,병미출현망상결구,이2∶1혼합배양조24 h 후가견내피세포상호련접성망상결구,출현전형적“성혈관현상”,차형성적혈관양결구명현다우대조조;심기세포조망수교대조조소。결론:골수원성심기세포여골수원성내피세포연합충식우 Matrigel 기질효공배양,가우체외성공구건혈관화조직공정심기。
Obj ective :To explore the feasibility of building vascularized tissue engineering myocardium in vitro .Methods :Bone marrow mesenchymal stem cells were induced to differentiate into cardiomyocytes by 5-aza and then labeled with DAPI. Bone marrow-derived endothelial progenitor cells were induced to differentiate into endothelial cells by EGM2-MV and then labeled with CM-dil.Four million labeled cardiomyocyte cells and endothelial cells were seeded at 2 ∶ 1 ratio on Matrigel matrix glue composite as a test group,and cardiomyocyte cells were seeded onto the same kind of composite as a control group.We observed the complex morphology,cell distribution and so on.Results :In the test group where cardiomyocyte cells and endothelial cells were mixed at 2∶1 ,typical “vascular phenomenon”of endothelial cells appeared after their culture 24 h,the number of capillary-like structure was significantly higher than the control group,but myocardium apoptosis decreased compared with the control group.Conclusion:Co-culture of the bone marrow-derived endothelial progenitor cells and marrow-derived cardiac cells can successfully build vascularized tissue engineering myocardium in vitro.