Rodrigues Márcia T, Leonor Isabel B, Gröen Nathalie, Viegas Carlos A, Dias Isabel R, Caridade Sofia G, Mano João F, Gomes Manuela E, Reis Rui L
3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4806-909 Taipas, Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
3B's Research Group - Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4806-909 Taipas, Guimarães, Portugal; ICVS/3B's - PT Government Associate Laboratory, Braga/Guimarães, Portugal.
Acta Biomater. 2014 Oct;10(10):4175-85. doi: 10.1016/j.actbio.2014.05.026. Epub 2014 Jun 4.
Osteogenic differentiation is a tightly regulated process dependent on the stimuli provided by the micro-environment. Silicon-substituted materials are known to have an influence on the osteogenic phenotype of undifferentiated and bone-derived cells. This study aims to investigate the bioactivity profile as well as the mechanical properties of a blend of starch and poly-caprolactone (SPCL) polymeric fiber mesh scaffolds functionalized with silanol (Si-OH) groups as key features for bone tissue engineering strategies. The scaffolds were made from SPCL by a wet spinning technique. A calcium silicate solution was used as a non-solvent to develop an in situ functionalization with Si-OH groups in a single-step approach. We also explored the relevance of silicon incorporated in SPCL-Si scaffolds to the in vitro osteogenic process of goat bone marrow stromal cells (gBMSCs) with and without osteogenic supplements in the culture medium. We hypothesized that SPCL-Si scaffolds could act as physical and chemical millieus to induce per se the osteogenic differentiation of gBMSCs. Results show that osteogenic differentiation of gBMSCs and the production of a mineralized extracellular matrix on bioactive SPCL-Si scaffolds occur for up to 2weeks, even in the absence of osteogenic supplements in the culture medium. The omission of media supplements to induce osteogenic differentiation is a promising feature towards simplified and cost-effective cell culturing procedures of a potential bioengineered product, and concomitant translation into the clinical field. Thus, the present work demonstrates that SPCL-Si scaffolds and their intrinsic properties sustain gBMSC osteogenic features in vitro, even in the absence of osteogenic supplements to the culture medium, and show great potential for bone regeneration strategies.
成骨分化是一个严格调控的过程,依赖于微环境提供的刺激。已知含硅取代材料会对未分化细胞和骨源细胞的成骨表型产生影响。本研究旨在探究淀粉与聚己内酯(SPCL)聚合物纤维网状支架混合物的生物活性特征以及机械性能,该支架用硅醇(Si-OH)基团功能化,这是骨组织工程策略的关键特征。支架由SPCL通过湿法纺丝技术制成。使用硅酸钙溶液作为非溶剂,以一步法实现与Si-OH基团的原位功能化。我们还探讨了SPCL-Si支架中所含硅对山羊骨髓基质细胞(gBMSC)在有或无培养基中成骨补充剂情况下体外成骨过程的相关性。我们假设SPCL-Si支架可作为物理和化学环境,本身诱导gBMSC的成骨分化。结果表明,即使在培养基中没有成骨补充剂的情况下,gBMSC在生物活性SPCL-Si支架上的成骨分化和矿化细胞外基质的产生可持续长达2周。省略诱导成骨分化的培养基补充剂是朝着简化和具有成本效益的潜在生物工程产品细胞培养程序以及向临床领域转化的一个有前景的特征。因此,目前的工作表明,SPCL-Si支架及其固有特性即使在培养基中没有成骨补充剂的情况下也能在体外维持gBMSC的成骨特征,并显示出骨再生策略的巨大潜力。