期刊
BIOMATERIALS
卷 32, 期 3, 页码 760-768出版社
ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2010.09.042
关键词
Runx2; Osterix; Gene transfer; Adipose stem cells; Osteogenesis
资金
- National Research Foundation of Korea [2010-0000305]
In the present study we tested the hypothesis that electroporation-mediated transfer of Runx2 Osterix or both genes enhances the in vitro and in vivo osteogenesis from adipose stem cells (ASCs) ASCs were transfected with Runx2 Osterix or both genes using electroporation and further cultured in monolayer or in PLGA scaffold under osteogenic medium for 14 days then analyzed for in vitro osteogenic differentiation Transfected ASC-PLGA scaffold hybrids were also implanted on nude mice to test for in vivo ectopic bone formation Runx2 and Osterix genes were strongly expressed in ASCs transfected with each gene on day 7 decreasing rapidly on day 14 Runx2 protein was strongly expressed in ASCs transfected with the Runx2 gene while Osterix protein was strongly expressed in ASCs transfected with either or both Runx2 and Osterix genes Overexpression of Runx2 and Osterix significantly increased the gene expression of osteogenic differentiation markers (alkaline phosphatase [ALP] osteocalcin [OCN] type I collagen [COL1A1] and bone sialoprotein [BSP]) in ASCs Transfection of Runx2 and Osterix genes enhanced the protein expression of OCN type I collagen and BSP as demonstrated by Western blot analysis and ALP activity as well as enhancing mineralization in the monolayer culture and ASC-PLGA scaffold hybrids Runx2- or Osterix-transfected ASC-PLGA scaffold hybrids promoted bone formation in nude mice after 6 weeks of in vivo implantation (C) 2010 Elsevier Ltd All rights reserved
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