中国骨质疏松杂志
中國骨質疏鬆雜誌
중국골질소송잡지
CHINESE JOURNAL OF OSTEOPOROSIS
2014年
8期
885-889
,共5页
卞铁荣%王莉丽%邢宏运%唐利
卞鐵榮%王莉麗%邢宏運%唐利
변철영%왕리려%형굉운%당리
HA-玻璃涂层/多孔ZrO2支架%诱导剂%骨髓间充质干细胞%成骨细胞
HA-玻璃塗層/多孔ZrO2支架%誘導劑%骨髓間充質榦細胞%成骨細胞
HA-파리도층/다공ZrO2지가%유도제%골수간충질간세포%성골세포
HA-glass coating/porous ZrO2 stents%Inducers%Bone marrow mesenchymal stem cells%Osteoblasts
目的:探讨生物复合材料HA-玻璃涂层/多孔ZrO2体外诱导分化SD大鼠乳鼠骨髓间充质干细胞为成骨细胞的能力,找到骨髓间充质干细胞理想的复合载体及移植后的安全性,为骨缺损的临床快速恢复治疗奠定基础。方法通过生物材料体外诱导SD大鼠骨髓间充质干细胞,培养至14天、21天,经Gomori钙钴法染色、Von Kossa染色及Ⅰ型胶原免疫组化分析比较诱导前后其碱性磷酸酶、钙结节、Ⅰ型胶原的表达变化;流式细胞技术检测诱导前后细胞CD45、CD44及CD90的表达变化。结果 SD大鼠骨髓间充质干细胞体外诱导14天,出现了三角形或不规则细胞,细胞之间界限清晰,碱性磷酸酶呈阳性表达;诱导至21天,细胞中出现致密圆形的矿化结节及Ⅰ型胶原呈阳性表达,细胞之间界限模糊;流式技术检测诱导前后细胞表面CD44仍为阳性表达, CD45仍为阴性表达,而CD90由原来的阳性表达转为阴性表达,细胞表达阳性率由99.7%下降为0.29%。结论该生物复合材料将骨髓间充质干细胞成功诱导为成骨细胞,且该材料又能与骨形成很强的化学结合,用作骨缺损的填充材料,为新骨的形成提供支架,发挥骨传导作用。
目的:探討生物複閤材料HA-玻璃塗層/多孔ZrO2體外誘導分化SD大鼠乳鼠骨髓間充質榦細胞為成骨細胞的能力,找到骨髓間充質榦細胞理想的複閤載體及移植後的安全性,為骨缺損的臨床快速恢複治療奠定基礎。方法通過生物材料體外誘導SD大鼠骨髓間充質榦細胞,培養至14天、21天,經Gomori鈣鈷法染色、Von Kossa染色及Ⅰ型膠原免疫組化分析比較誘導前後其堿性燐痠酶、鈣結節、Ⅰ型膠原的錶達變化;流式細胞技術檢測誘導前後細胞CD45、CD44及CD90的錶達變化。結果 SD大鼠骨髓間充質榦細胞體外誘導14天,齣現瞭三角形或不規則細胞,細胞之間界限清晰,堿性燐痠酶呈暘性錶達;誘導至21天,細胞中齣現緻密圓形的礦化結節及Ⅰ型膠原呈暘性錶達,細胞之間界限模糊;流式技術檢測誘導前後細胞錶麵CD44仍為暘性錶達, CD45仍為陰性錶達,而CD90由原來的暘性錶達轉為陰性錶達,細胞錶達暘性率由99.7%下降為0.29%。結論該生物複閤材料將骨髓間充質榦細胞成功誘導為成骨細胞,且該材料又能與骨形成很彊的化學結閤,用作骨缺損的填充材料,為新骨的形成提供支架,髮揮骨傳導作用。
목적:탐토생물복합재료HA-파리도층/다공ZrO2체외유도분화SD대서유서골수간충질간세포위성골세포적능력,조도골수간충질간세포이상적복합재체급이식후적안전성,위골결손적림상쾌속회복치료전정기출。방법통과생물재료체외유도SD대서골수간충질간세포,배양지14천、21천,경Gomori개고법염색、Von Kossa염색급Ⅰ형효원면역조화분석비교유도전후기감성린산매、개결절、Ⅰ형효원적표체변화;류식세포기술검측유도전후세포CD45、CD44급CD90적표체변화。결과 SD대서골수간충질간세포체외유도14천,출현료삼각형혹불규칙세포,세포지간계한청석,감성린산매정양성표체;유도지21천,세포중출현치밀원형적광화결절급Ⅰ형효원정양성표체,세포지간계한모호;류식기술검측유도전후세포표면CD44잉위양성표체, CD45잉위음성표체,이CD90유원래적양성표체전위음성표체,세포표체양성솔유99.7%하강위0.29%。결론해생물복합재료장골수간충질간세포성공유도위성골세포,차해재료우능여골형성흔강적화학결합,용작골결손적전충재료,위신골적형성제공지가,발휘골전도작용。
Objective To explore the ability of the biological composite materials, HA-glass coating/porous ZrO2, inducing SD rat bone marrow mesenchymal stem cells to differentiate into osteoblasts in vitro, to find the ideal composite carrier of transplantated bone marrow mesenchymal stem cells and to investigate the security after transplantation, and to lay foundation for the fast recovery treatment of bone defect.Methods SD rat bone marrow mesenchymal stem cells were induced to differentiate by biological materials in vitro.Then cells were cultured for 14 days and 21 days.After dying with calcium-cobalt according to Gomori, Von Kossa staining, and immunohistochemical technology, the expression of alkaline phosphatase, calcium nodules, and type I collagen was detected.The changes of the expression of CD45, CD44, and CD90 in the cells before and after the induction were detected using flow cytometry.Results After 14-day induction in vitro, the cell morphology of SD rat bone marrow mesenchymal stem cells changed from long shuttle deformation cells to triangle or polygon cells, and there were clear boundaries between the cells.The expression of alkaline phosphatase was positive.After 21-day induction, dense and circular mineralized nodules appeared in cells, and the expression of type I collagen was positive.The boundaries between cells were blurred.According to the results of flow cytometry technology, the expression of CD44 was still positive, and the expression of CD45 was still negative.But the expression of CD90 transformed from positive to negative.The positive expression rate of cells decreased from 99.7%to 0.29%.Conclusion Biological composite materials, HA-glass coating/porous ZrO2 scaffolds, successfully induce SD rat bone marrow mesenchymal stem cells to osteoblasts.These materials can combine with bone formation through strong chemical bond, which can be used as bone defect filling materials, and provide support for the formation of new bone, and play the conduction role in bone.