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Optimization of release pattern of FGF-2 and BMP-2 for osteogenic differentiation of low-population density hMSCs
L. Lei; S. Wang; H. H. Wu; W. Ju; J. Peng; A. S. A. Qahtan; C. Chen; Y. Q. Lu; J. Y. Peng; X. Zhang; H. M. Nie
2015
Source PublicationJournal of Biomedical Materials Research Part A
ISSN1549-3296
Volume103Issue:1Pages:252-261
AbstractIn the modern design, most delivery systems for bone regeneration focus on a single growth factor (GF) or a simple mixture of multiple GFs, overlooking the coordination of proliferation and osteogenesis induced by various factors. In this study, core-shell microspheres with poly-l-lactide core-poly(lactic-co-glycolic acid) shell were fabricated, and two GFs, basic fibroblast growth factor 2 (FGF-2) and bone morphogenetic protein 2 (BMP-2) were encapsulated into the core or/and shell. The effects of different release patterns (parallel or sequential manners) of FGF-2 and BMP-2 from these core-shell microspheres on the osteogenic differentiation of low-population density human mesenchymal stem cells (hMSCs) were investigated and the temporal organization of GF release was optimized. In vitro experiments suggested that induction of osteogenic differentiation of low-population density hMSCs by the sequential delivery of FGF-2 followed by BMP-2 from the core-shell microspheres (group S2) was much more efficient than that by the parallel release of the two factors from uniform microspheres (group U). The osteogenic induction by the sequential delivery of BMP-2 followed by FGF-2 from core-shell microspheres (group S1) was even worse than that from microspheres loaded with BMP-2 in both core and shell (group B), although comparable to the cases of parallel delivery of dual GFs (group P). This study showed the advantages of group S2 microspheres in inducing osteogenic differentiation of low-population density hMSCs and the necessity of time sequence studies in tissue engineering while multiple GFs are involved. (c) 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 252-261, 2015.
description.department[lei, lei ; peng, jieying] cent s univ, xiangya hosp, dept stomatol, changsha 410008, hunan, peoples r china. [wang, shuo ; wu, honghui ; ju, wei ; peng, jian ; qahtan, anwar saeed ahmed ; nie, hemin] hunan univ, dept biomed engn, coll biol, changsha 410082, hunan, peoples r china. [chen, chen] beijing univ chem technol, dept mat sci & engn, coll mat sci & engn, beijing 100029, peoples r china. [lu, yanqin] cent s univ, xiangya stomatol hosp, dept orthodont, changsha 410008, hunan, peoples r china. [zhang, xing] chinese acad sci, shenyang natl lab mat sci, inst met res, shenyang 110016, peoples r china. ; nie, hm (reprint author), hunan univ, dept biomed engn, coll biol, changsha 410082, hunan, peoples r china. ; niehemin@hnu.edu.cn
KeywordFgf-2 Bmp-2 Core-shell Microsphere Sequential Release Osteogenic Differentiation Fibroblast-growth-factor Drug-delivery Bone-marrow Cell-death Nanoparticles Regeneration Migration System Rats Dna
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Language英语
Document Type期刊论文
Identifierhttp://ir.imr.ac.cn/handle/321006/73259
Collection中国科学院金属研究所
Recommended Citation
GB/T 7714
L. Lei,S. Wang,H. H. Wu,et al. Optimization of release pattern of FGF-2 and BMP-2 for osteogenic differentiation of low-population density hMSCs[J]. Journal of Biomedical Materials Research Part A,2015,103(1):252-261.
APA L. Lei.,S. Wang.,H. H. Wu.,W. Ju.,J. Peng.,...&H. M. Nie.(2015).Optimization of release pattern of FGF-2 and BMP-2 for osteogenic differentiation of low-population density hMSCs.Journal of Biomedical Materials Research Part A,103(1),252-261.
MLA L. Lei,et al."Optimization of release pattern of FGF-2 and BMP-2 for osteogenic differentiation of low-population density hMSCs".Journal of Biomedical Materials Research Part A 103.1(2015):252-261.
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