Human mesenchymal progenitor cell-based tissue engineering of a single-unit osteochondral construct

被引:85
作者
Tuli, R
Nandi, S
Li, WJ
Tuli, S
Huang, XX
Manner, PA
Laquerriere, P
Nöth, U
Hall, DJ
Tuan, RS
机构
[1] NIAMSD, Cartilage Biol & Orthoped Branch, NIH, US Dept HHS, Bethesda, MD 20892 USA
[2] Thomas Jefferson Univ, Grad Program Cell & Tissue Engn, Philadelphia, PA USA
[3] George Washington Univ, Med Ctr, Dept Orthoped Surg, Washington, DC 20037 USA
[4] NIH, Div Bioengn & Phys Sci, Off Res Serv, Bethesda, MD 20892 USA
[5] Univ Wurzburg, Dept Orthoped Surg, Wurzburg, Germany
来源
TISSUE ENGINEERING | 2004年 / 10卷 / 7-8期
关键词
D O I
10.1089/ten.2004.10.1169
中图分类号
Q813 [细胞工程];
学科分类号
摘要
A desirable strategy for articular cartilage repair is to surgically replace the damaged area with an in vitro-engineered osteochondral plug. We report here the development of a novel osteochondral construct using human trabecular bone-derived mesenchymal progenitor cells and a biodegradable poly-D,L-lactic acid scaffold. The cartilage layer was fabricated by press-coating a chondrifying high-density cell pellet onto the scaffold, which was then loaded with cells previously initiated to undergo osteogenesis. The composite was then cultured in a cocktail medium formulated to maintain both chondrogenesis and osteogenesis. Macroscopically, the construct consisted of a cartilage-like layer adherent to, and overlying, a dense bone-like component. RT-PCR, immunohistochemistry, and histology revealed hyaline-like cartilage and bone with an interface resembling the native osteochondral junction. All parameters, including mechanical properties, improved with increased culture time. The single-cell source nature of the construct, which minimizes handling while maximizing biocompatibility, suggests applicability for articular cartilage repair.
引用
收藏
页码:1169 / 1179
页数:11
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