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
10期
1629-1634
,共6页
唐丽%武俊杰%王阿娴%梁源%季海宁%丁寅
唐麗%武俊傑%王阿嫻%樑源%季海寧%丁寅
당려%무준걸%왕아한%량원%계해저%정인
干细胞%培养%细胞外基质%骨髓细胞%人牙周膜干细胞%微环境%脱细胞%国家自然科学基金
榦細胞%培養%細胞外基質%骨髓細胞%人牙週膜榦細胞%微環境%脫細胞%國傢自然科學基金
간세포%배양%세포외기질%골수세포%인아주막간세포%미배경%탈세포%국가자연과학기금
stem cells%extracellular matrix%bone marrow cells
背景:细胞外基质可以在体外模拟细胞微环境,使干细胞在体外大量增殖的同时具有良好的干细胞特性。目的:制备人骨髓细胞外基质并分析其结构成分。<br> 方法:取第4代人骨髓细胞培养14 d,在最后8 d换成膜诱导液,经脱细胞处理后制备人骨髓细胞外基质。倒置显微镜和扫描电镜观察人骨髓细胞外基质表面形态。免疫荧光染色观察脱细胞处理前后Ⅰ型胶原和二聚糖的变化。将人牙周膜干细胞接种于人骨髓细胞外基质、纤粘连蛋白包被的六孔板和普通培养板,比较不同基质对人牙周膜干细胞细胞形态和黏附的影响。<br> 结果与结论:化学物理联合脱细胞处理可以获得结构完整的人骨髓细胞外基质膜片,Ⅰ型胶原和二聚糖在去细胞处理前后结构和含量无明显差异。接种在细胞外基质上生长的人牙周膜干细胞,按照细胞外基质的轨道有序生长,不同于原有细胞形态;相同时间人牙周膜干细胞在细胞外基质上贴壁数量较多。表明有效的脱细胞处理可以得到结构完整的细胞外基质网状支架,相关蛋白成分未因脱细胞而明显丧失,细胞外基质影响接种细胞的形态、促进细胞黏附。提示可利用细胞外基质模型模拟体内干细胞生长微环境,在体外获得大量高质量的成体干细胞。
揹景:細胞外基質可以在體外模擬細胞微環境,使榦細胞在體外大量增殖的同時具有良好的榦細胞特性。目的:製備人骨髓細胞外基質併分析其結構成分。<br> 方法:取第4代人骨髓細胞培養14 d,在最後8 d換成膜誘導液,經脫細胞處理後製備人骨髓細胞外基質。倒置顯微鏡和掃描電鏡觀察人骨髓細胞外基質錶麵形態。免疫熒光染色觀察脫細胞處理前後Ⅰ型膠原和二聚糖的變化。將人牙週膜榦細胞接種于人骨髓細胞外基質、纖粘連蛋白包被的六孔闆和普通培養闆,比較不同基質對人牙週膜榦細胞細胞形態和黏附的影響。<br> 結果與結論:化學物理聯閤脫細胞處理可以穫得結構完整的人骨髓細胞外基質膜片,Ⅰ型膠原和二聚糖在去細胞處理前後結構和含量無明顯差異。接種在細胞外基質上生長的人牙週膜榦細胞,按照細胞外基質的軌道有序生長,不同于原有細胞形態;相同時間人牙週膜榦細胞在細胞外基質上貼壁數量較多。錶明有效的脫細胞處理可以得到結構完整的細胞外基質網狀支架,相關蛋白成分未因脫細胞而明顯喪失,細胞外基質影響接種細胞的形態、促進細胞黏附。提示可利用細胞外基質模型模擬體內榦細胞生長微環境,在體外穫得大量高質量的成體榦細胞。
배경:세포외기질가이재체외모의세포미배경,사간세포재체외대량증식적동시구유량호적간세포특성。목적:제비인골수세포외기질병분석기결구성분。<br> 방법:취제4대인골수세포배양14 d,재최후8 d환성막유도액,경탈세포처리후제비인골수세포외기질。도치현미경화소묘전경관찰인골수세포외기질표면형태。면역형광염색관찰탈세포처리전후Ⅰ형효원화이취당적변화。장인아주막간세포접충우인골수세포외기질、섬점련단백포피적륙공판화보통배양판,비교불동기질대인아주막간세포세포형태화점부적영향。<br> 결과여결론:화학물리연합탈세포처리가이획득결구완정적인골수세포외기질막편,Ⅰ형효원화이취당재거세포처리전후결구화함량무명현차이。접충재세포외기질상생장적인아주막간세포,안조세포외기질적궤도유서생장,불동우원유세포형태;상동시간인아주막간세포재세포외기질상첩벽수량교다。표명유효적탈세포처리가이득도결구완정적세포외기질망상지가,상관단백성분미인탈세포이명현상실,세포외기질영향접충세포적형태、촉진세포점부。제시가이용세포외기질모형모의체내간세포생장미배경,재체외획득대량고질량적성체간세포。
BACKGROUND:Extracellular matrix can simulate microenvironment and make the stem cells proliferate maintaining the characteristics of stem cells wel in vitro. OBJECTIVE:To prepare the extracellular matrix from human bone marrow cells and to analyze its microstructure and composition preliminarily. METHODS:Human bone marrow cells of passage 4 were cultured for 14 days, and the induction medium was used during the last 8 days. After decellularization, cells were removed to prepare human bone marrow cells-derived extracellular matrix. The surface morphology of human bone marrow cells-derived extracellular matrix was observed by inverted microscope and scanning electron microscope. Changes of col agen I and biglycan before and after decellularization were observed by immunofluorescence staining. Human periodontal ligament stem cells were seeded onto human bone marrow cells-derived extracellular matrix, fibronectin coated 6-wel plate and normal culture plate to compare the influence of different matrix on cellmorphology and adhesion. RESULTS AND CONCLUSION:We obtained intact human bone marrow cells-derived extracellular matrix by chemical combined with physical decellularization. The structure and amount of col agen I and biglycan had not been compromised dramatical y after decellularization. Human periodontal ligament stem cells growing on the human bone marrow cells-derived extracellular matrix developed in accordance with the orbit of the extracellular matrix, differing from the original cellmorphology. There were more human periodontal ligament stem cells adhering to the extracellular matrix during the same time. These findings indicate that effective decellularization can produce intact the extracellular matrix membrane without destroying its microstructure. Extracellular matrix protein is not compromised due to decellularization. The extracellular matrix affects cellmorphology and promotes celladhesion. We can use the extracellular matrix model to simulate stem cellmicroenvironment and thereafter, acquire a large number of adult stem cells with high quality in vitro.