Three-dimensionalenvironment and vascularization induce osteogenic maturation of human adipose-derived stem cells comparable to that of bone-derived progenitors

被引:9
作者
Ibrahim, Amel [1 ,2 ]
Rodriguez-Florez, Naiara [1 ,2 ,3 ]
Gardner, Oliver F. W. [1 ]
Zucchelli, Eleonora [1 ]
New, Sophie E. P. [1 ]
Borghi, Alessandro [1 ,2 ]
Dunaway, David [1 ,2 ]
Bulstrode, Neil W. [2 ]
Ferretti, Patrizia [1 ]
机构
[1] UCL Great Ormond St Inst Child Hlth, Stem Cells & Regenerat Med Sect, London, England
[2] Great Ormond St Hosp Children NHS Fdn Trust, Dept Plast Surg, London, England
[3] Univ Navarra, TECNUN Escuela Ingn, San Sebastian, Spain
基金
欧洲研究理事会;
关键词
3D environment; bone; differentiation; human adipose-derived stem cells; mesenchymal stem cells; osteogenesis; progenitor cells; tissue engineering; vascularization; MESENCHYMAL STROMAL CELLS; OSTEOBLAST DIFFERENTIATION; ENDOTHELIAL-CELLS; IN-VITRO; MARROW; RECONSTRUCTION; SCAFFOLDS; PROTEINS; CULTURE; EXPRESSION;
D O I
10.1002/sctm.19-0207
中图分类号
Q813 [细胞工程];
学科分类号
摘要
While human adipose-derived stem cells (hADSCs) are known to possess osteogenic differentiation potential, the bone tissues formed are generally considered rudimentary and immature compared with those made by bone-derived precursor cells such as human bone marrow-derived mesenchymal stem cells (hBMSCs) and less commonly studied human calvarium osteoprogenitor cells (hOPs). Traditional differentiation protocols have tended to focus on osteoinduction of hADSCs through the addition of osteogenic differentiation media or use of stimulatory bioactive scaffolds which have not resulted in mature bone formation. Here, we tested the hypothesis that by reproducing the physical as well as biochemical bone microenvironment through the use of three-dimensional (3D) culture and vascularization we could enhance osteogenic maturation in hADSCs. In addition to biomolecular characterization, we performed structural analysis through extracellular collagen alignment and mineral density in our bone tissue engineered samples to evaluate osteogenic maturation. We further compared bone formed by hADSCs, hBMSCs, and hOPs against mature human pediatric calvarial bone, yet not extensively investigated. Although bone generated by all three cell types was still less mature than native pediatric bone, a fibrin-based 3D microenvironment together with vascularization boosted osteogenic maturation of hADSC making it similar to that of bone-derived osteoprogenitors. This demonstrates the important role of vascularization and 3D culture in driving osteogenic maturation of cells easily available but constitutively less committed to this lineage and suggests a crucial avenue for recreating the bone microenvironment for tissue engineering of mature craniofacial bone tissues from pediatric hADSCs, as well as hBMSCs and hOPs.
引用
收藏
页码:1651 / 1666
页数:16
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