中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2015年
28期
4455-4459
,共5页
高明杰%陶杰%周孜辉%杜琳
高明傑%陶傑%週孜輝%杜琳
고명걸%도걸%주자휘%두림
干细胞%骨髓干细胞%生物衍生骨材料%骨髓间充质干细胞%细胞毒性%生物相容性%复合培养
榦細胞%骨髓榦細胞%生物衍生骨材料%骨髓間充質榦細胞%細胞毒性%生物相容性%複閤培養
간세포%골수간세포%생물연생골재료%골수간충질간세포%세포독성%생물상용성%복합배양
背景:异种生物衍生骨保存了原骨组织的天然网状孔隙结构,且具有免疫原性低、细胞相容性好的特点。目的:验证异种生物衍生骨材料与骨髓间充质干细胞的生物相容性。<br> 方法:取新鲜猪股骨制备生物衍生骨,扫描电镜观察材料结构。将第3代兔骨髓间充质干细胞以2×109 L-1的浓度接种于生物衍生骨材料的松质骨面,复合培养7d内,采用扫描电镜观察细胞生长情况;复合培养8d内,计数材料上附着的细胞数。<br> 结果与结论:生物衍生骨表面粗糙,孔隙不规则并相互通联,构成网状结构。复合培养3 d,细胞在衍生骨材料表面发生附着,且细胞形态不均一;复合培养培养5 d,细胞连接成片呈层状生长,细胞之间紧密接触;复合培养7 d,细胞呈现多层生长状态,成堆生长,部分区域存在细胞外基质分泌现象。复合培养后,前2 d 为潜伏适应期,3-6d细胞生长呈出线性曲线,处于细胞生长对数期;第6天后,细胞生长曲线逐渐变得平缓,细胞增殖速度下降,增殖进入平台期。表明异种生物衍生骨材料与骨髓间充质干细胞具有良好的生物相容性。
揹景:異種生物衍生骨保存瞭原骨組織的天然網狀孔隙結構,且具有免疫原性低、細胞相容性好的特點。目的:驗證異種生物衍生骨材料與骨髓間充質榦細胞的生物相容性。<br> 方法:取新鮮豬股骨製備生物衍生骨,掃描電鏡觀察材料結構。將第3代兔骨髓間充質榦細胞以2×109 L-1的濃度接種于生物衍生骨材料的鬆質骨麵,複閤培養7d內,採用掃描電鏡觀察細胞生長情況;複閤培養8d內,計數材料上附著的細胞數。<br> 結果與結論:生物衍生骨錶麵粗糙,孔隙不規則併相互通聯,構成網狀結構。複閤培養3 d,細胞在衍生骨材料錶麵髮生附著,且細胞形態不均一;複閤培養培養5 d,細胞連接成片呈層狀生長,細胞之間緊密接觸;複閤培養7 d,細胞呈現多層生長狀態,成堆生長,部分區域存在細胞外基質分泌現象。複閤培養後,前2 d 為潛伏適應期,3-6d細胞生長呈齣線性麯線,處于細胞生長對數期;第6天後,細胞生長麯線逐漸變得平緩,細胞增殖速度下降,增殖進入平檯期。錶明異種生物衍生骨材料與骨髓間充質榦細胞具有良好的生物相容性。
배경:이충생물연생골보존료원골조직적천연망상공극결구,차구유면역원성저、세포상용성호적특점。목적:험증이충생물연생골재료여골수간충질간세포적생물상용성。<br> 방법:취신선저고골제비생물연생골,소묘전경관찰재료결구。장제3대토골수간충질간세포이2×109 L-1적농도접충우생물연생골재료적송질골면,복합배양7d내,채용소묘전경관찰세포생장정황;복합배양8d내,계수재료상부착적세포수。<br> 결과여결론:생물연생골표면조조,공극불규칙병상호통련,구성망상결구。복합배양3 d,세포재연생골재료표면발생부착,차세포형태불균일;복합배양배양5 d,세포련접성편정층상생장,세포지간긴밀접촉;복합배양7 d,세포정현다층생장상태,성퇴생장,부분구역존재세포외기질분비현상。복합배양후,전2 d 위잠복괄응기,3-6d세포생장정출선성곡선,처우세포생장대수기;제6천후,세포생장곡선축점변득평완,세포증식속도하강,증식진입평태기。표명이충생물연생골재료여골수간충질간세포구유량호적생물상용성。
BACKGROUND:Bio-derived xenograft bone has natural pore structure of the bone, low immunogenicity, and good cytocompatibility. <br> OBJECTIVE:To verify the biocompatibility of bio-derived xenograft bone with bone marrow mesenchymal stem cel s. <br> METHODS:Fresh pig femoral bone was col ected to prepare bio-derived bone. Scanning electron microscope was used to observe the material structure. Passage 3 rabbit bone marrow mesenchymal stem cel s at a density of 2×109/L were inoculated into the cancel ous bone surface of the bio-dervied bone and cultured for 7 days. Cel growth was detected using scanning electron microscope. After culture for 8 days, cel number was counted. <br> RESULTS AND CONCLUSION:The bio-derived bone had rough surface and irregularly interconnected pores constructing a mesh-like structure. After 3 days of compound culture, cel s had irregular shapes and adhered to the surface of bio-derived bone;after 5 days of culture, cel s were closely interconnected to form a layered growth;after 7 days of culture, cel s exhibited multilayered growth and the extracel ular matrix secreted local y. Under compound culture, the former 2 days were latent period, 3-6 days were logarithmic phase, and from the 6 th day, the cel growth curve became smooth gradual y and the cel proliferation decreased and entered into the plateau period. These findings indicate that the bio-derived xenograft bone has good biocompatibility with bone marrow mesenchymal stem cel s.