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Use of bone morphogenetic proteins in mesenchymal stemcell stimulation of cartilage and bone repair 被引量:22
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作者 Sonia Scarfì 《World Journal of Stem Cells》 SCIE CAS 2016年第1期1-12,共12页
The extracellular matrix-associated bone morphogenetic proteins(BMPs) govern a plethora of biological processes. The BMPs are members of the transforming growth factor-β protein superfamily, and they actively partici... The extracellular matrix-associated bone morphogenetic proteins(BMPs) govern a plethora of biological processes. The BMPs are members of the transforming growth factor-β protein superfamily, and they actively participate to kidney development, digit and limb formation, angiogenesis, tissue fibrosis and tumor development. Since their discovery, they have attracted attention for their fascinating perspectives in the regenerative medicine and tissue engineering fields. BMPs have been employed in many preclinical and clinical studies exploring their chondrogenic or osteoinductive potential in several animal model defects and in human diseases. During years of research in particular two BMPs, BMP2 and BMP7 have gained the podium for their use in the treatment of various cartilage and bone defects. In particular they have been recently approved for employment in non-union fractures as adjunct therapies. On the other hand, thanks to their potentialities in biomedical applications, there is a growing interest in studying the biology of mesenchymal stem cell(MSC), the rules underneath their differentiation abilities, and to test their true abilities in tissue engineering. In fact, the specific differentiation of MSCs into targeted celltype lineages for transplantation is a primary goal of the regenerative medicine. This review provides an overview on the current knowledge of BMP roles and signaling in MSC biology and differentiation capacities. In particular the article focuses on the potential clinical use of BMPs and MSCs concomitantly, in cartilage and bone tissue repair. 展开更多
关键词 MESENCHYMAL stem cells CARTILAGE bonerepair BONE morphogenetic PROTEIN
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负载BMP-2和BSA的丝素蛋白/聚左旋乳酸-己内酯三维纤维屏障膜的制备及性能 被引量:1
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作者 杨少华 何苗苗 +5 位作者 常语宸 孙睿 吕晓琴 王开娟 殷丽华 余占海 《复合材料学报》 EI CAS CSCD 北大核心 2017年第12期2810-2818,共9页
利用骨形态发生蛋白-2(BMP-2)的骨诱导作用和牛血清白蛋白(BSA)的稳定作用,结合同轴静电纺丝技术和共混静电纺丝技术,制备了三组纤维膜,包括同时携载BMP-2和BSA的丝素蛋白(SF)/聚左旋乳酸-己内酯(PLCL)同轴载药纤维膜(BMP-2-BSA@SF/PLCL... 利用骨形态发生蛋白-2(BMP-2)的骨诱导作用和牛血清白蛋白(BSA)的稳定作用,结合同轴静电纺丝技术和共混静电纺丝技术,制备了三组纤维膜,包括同时携载BMP-2和BSA的丝素蛋白(SF)/聚左旋乳酸-己内酯(PLCL)同轴载药纤维膜(BMP-2-BSA@SF/PLCL,Mat A);同时携载BMP-2和BSA的SF/PLCL共混载药纤维膜(BMP-2-BSA-SF/PLCL,Mat B)和非载药SF/PLCL纤维膜(SF/PLCL,Mat C)。通过研究纤维膜的表观形态,得出三种纤维膜均呈均匀网状结构,其中Mat A组具有稳定的核层结构;理化性能研究证实三组纤维的接触角和力学性能依次增大;体外细胞实验和膜屏障实验表明,三组纤维膜均具有良好的生物相容性和屏障功能,且具有药物缓释作用的组纤Mat A维膜能够更加有效地刺激细胞生长和早期骨向分化。所制备的BMP-2-BSA@SF/PLCL能够满足引导性骨组织再生(GBR)生物膜的基本要求,是促进骨缺损修复的理想载体。 展开更多
关键词 同轴静电纺丝 引导性骨组织再生 生物膜 骨形态发生蛋白-2 骨修复
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