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
30期
4863-4867
,共5页
生物材料%骨生物材料%成骨细胞%细胞外基质%脱细胞方法%胰酶法%冻融法
生物材料%骨生物材料%成骨細胞%細胞外基質%脫細胞方法%胰酶法%凍融法
생물재료%골생물재료%성골세포%세포외기질%탈세포방법%이매법%동융법
osteoblasts%extracellular matrix
背景:比起单一或复合的生物活性分子材料,脱细胞胞外基质更接近天然生物体内的细胞外环境,在组织工程中得到越来越多的重视和应用,但脱细胞方法会影响所得胞外基质的结构和成分,目前缺少脱细胞方法对胞外基质影响的研究。目的:分析不同脱细胞方法所得胞外基质的成分和作为修饰表面对细胞生物学效应的影响。方法:取生长良好的第3代SD乳鼠成骨细胞,分别采用冻融法、胰酶法、去污剂法、弱碱法脱去细胞留下基质,形成4组胞外基质,通过酶联免疫吸附实验分析胞外基质的生物成分。分别在4组胞外基质表面接种成骨细胞,以常规培养的细胞为对照,进行MTT比色实验、碱性磷酸酶活性检测,对比5组成骨细胞的生物活动。结果与结论:冻融法组胶原成分与胞体残留成分较多,去污剂法组和弱碱法组次之,胰酶法组最少。冻融法组接种第3,5,7天的细胞A值高于对照组(P<0.05),去污剂法组接种第3,5,7天的细胞A值低于对照组(P <0.05)。胰酶法组接种第5,7天的细胞碱性磷酸酶活性低于对照组(P <0.05);弱碱法组接种第7天的细胞碱性磷酸酶活性低于对照组(P<0.05);去污剂法组接种第3,5,7天的细胞碱性磷酸酶活性低于对照组(P <0.05)。表明4种方法中,冻融法脱细胞能够获得更多的胞外基质,所构建基质涂层更有利于细胞的增殖。
揹景:比起單一或複閤的生物活性分子材料,脫細胞胞外基質更接近天然生物體內的細胞外環境,在組織工程中得到越來越多的重視和應用,但脫細胞方法會影響所得胞外基質的結構和成分,目前缺少脫細胞方法對胞外基質影響的研究。目的:分析不同脫細胞方法所得胞外基質的成分和作為脩飾錶麵對細胞生物學效應的影響。方法:取生長良好的第3代SD乳鼠成骨細胞,分彆採用凍融法、胰酶法、去汙劑法、弱堿法脫去細胞留下基質,形成4組胞外基質,通過酶聯免疫吸附實驗分析胞外基質的生物成分。分彆在4組胞外基質錶麵接種成骨細胞,以常規培養的細胞為對照,進行MTT比色實驗、堿性燐痠酶活性檢測,對比5組成骨細胞的生物活動。結果與結論:凍融法組膠原成分與胞體殘留成分較多,去汙劑法組和弱堿法組次之,胰酶法組最少。凍融法組接種第3,5,7天的細胞A值高于對照組(P<0.05),去汙劑法組接種第3,5,7天的細胞A值低于對照組(P <0.05)。胰酶法組接種第5,7天的細胞堿性燐痠酶活性低于對照組(P <0.05);弱堿法組接種第7天的細胞堿性燐痠酶活性低于對照組(P<0.05);去汙劑法組接種第3,5,7天的細胞堿性燐痠酶活性低于對照組(P <0.05)。錶明4種方法中,凍融法脫細胞能夠穫得更多的胞外基質,所構建基質塗層更有利于細胞的增殖。
배경:비기단일혹복합적생물활성분자재료,탈세포포외기질경접근천연생물체내적세포외배경,재조직공정중득도월래월다적중시화응용,단탈세포방법회영향소득포외기질적결구화성분,목전결소탈세포방법대포외기질영향적연구。목적:분석불동탈세포방법소득포외기질적성분화작위수식표면대세포생물학효응적영향。방법:취생장량호적제3대SD유서성골세포,분별채용동융법、이매법、거오제법、약감법탈거세포류하기질,형성4조포외기질,통과매련면역흡부실험분석포외기질적생물성분。분별재4조포외기질표면접충성골세포,이상규배양적세포위대조,진행MTT비색실험、감성린산매활성검측,대비5조성골세포적생물활동。결과여결론:동융법조효원성분여포체잔류성분교다,거오제법조화약감법조차지,이매법조최소。동융법조접충제3,5,7천적세포A치고우대조조(P<0.05),거오제법조접충제3,5,7천적세포A치저우대조조(P <0.05)。이매법조접충제5,7천적세포감성린산매활성저우대조조(P <0.05);약감법조접충제7천적세포감성린산매활성저우대조조(P<0.05);거오제법조접충제3,5,7천적세포감성린산매활성저우대조조(P <0.05)。표명4충방법중,동융법탈세포능구획득경다적포외기질,소구건기질도층경유리우세포적증식。
BACKGROUND:Compared with single or composite biomolecular materials, decellulazied matrices are more biomimetic to natural ectocytic surroundings. So cel-secreted extracellular matrix is paid more and more attention in the field of tissue engineering, and the composition of these matrices are influenced by decellulezired preparation methods more or less. But there are few studies about the biological effect of different decellulazried methods on the extracellular matrix. OBJECTIVE:To investigate the composition of cel-secreted extracellular matrices in vitro by different decellularizing methods and their effects as surface modification on cytobiological reaction. METHODS:After the treatment of different decellularizing methods (freeze/thaw cycles, trypsin, weak alkal, detergents), the extracellular matrix was obtained and grouped into four kinds. The biological composition of the extracellular matrix was determined by ELISA assay. Then osteoblasts were seeded onto the four kinds of extracellular matrix surfaces. cells cultured normal y served as controls. The effect of extracellular matrix coatings on cellgrowth and differentiation were determined by MTT test and alkaline phosphatase activity test. RESULTS AND CONCLUSION:The residual components were the most in the freeze-thaw group, fol owed by the detergent and weak alkal groups, and the least in the trypsin group. Compared with the control group, the absorbance value of cells were lower in the freeze-thaw and detergent groups at days 3, 5, 7 after inoculation (both P<0.05);the alkaline phosphatase activity was lower in the trypsin group at days 5, 7 after inoculation (P<0.05), in the weak alkal group at 7 days after inoculation (P<0.05), and in the detergent group at days 3, 5, 7 after inoculation (P<0.05). Therefore, we can harvest more extracellular matrices by the freeze-thaw method, and the extracellular matrix coating synthesized by the freeze-thaw method is more helpful for cellgrowth than others.