Laboratory for Skeletal Development and Joint Disorders, Katholieke Universiteit Leuven, Leuven, Belgium.
Tissue Eng Part C Methods. 2012 Feb;18(2):90-103. doi: 10.1089/ten.TEC.2011.0248. Epub 2011 Nov 2.
We report on the in vitro use of Ca(2+)/P(i) supplementation as a bio-instructive medium to drive human periosteum-derived cells (hPDCs) toward osteogenic differentiation on three-dimensional (3D) porous Ti6Al4V scaffolds. Through a multilevel factorial analysis, we have systematically investigated the biological effect and interactions of Ca(2+) or P(i) supplementation in three selected media preparations (i.e., basic growth medium, osteogenic medium [OM], and osteogenic medium without β-glycerophosphate [OM(-)]) and have identified specific conditions which induce proliferation and significant osteogenic differentiation of two-dimensional (2D) hPDC cultures. These findings were translated from 2D to 3D cultures conditions to instruct hPDCs to populate porous Ti6Al4V scaffolds and to differentiate into the osteoblast lineage with collagenous matrix production and subsequent matrix mineralization on the 3D structures. These osteogenic hybrids may potentially serve as a clinically relevant customizable bone reparative unit, providing a biomimetic template to more effectively mediate in vivo bone regeneration.
我们报告了体外使用 Ca(2+)/P(i) 补充作为生物指导介质,以促使人骨膜来源细胞 (hPDCs) 在三维 (3D) 多孔 Ti6Al4V 支架上向成骨分化。通过多层次析因分析,我们系统地研究了 Ca(2+) 或 P(i) 补充在三种选定的培养基制备中的生物学效应和相互作用(即基本生长培养基、成骨培养基 [OM] 和不含 β-甘油磷酸的成骨培养基 [OM(-)]),并确定了特定的条件,这些条件可诱导二维 (2D) hPDC 培养物的增殖和显著的成骨分化。这些发现从二维培养条件转化为三维培养条件,指导 hPDCs 在多孔 Ti6Al4V 支架上定殖,并分化为成骨细胞系,在三维结构上产生胶原基质和随后的基质矿化。这些成骨杂交体可能作为一种具有临床相关性的可定制的骨修复单元,为更有效地介导体内骨再生提供了仿生模板。