Ferraro Wally, Civilleri Aurelio, Gögele Clemens, Carbone Camilla, Vitrano Ilenia, Carfi Pavia Francesco, Brucato Valerio, La Carrubba Vincenzo, Werner Christian, Schäfer-Eckart Kerstin, Schulze-Tanzil Gundula
Engineering Department, Università degli Studi di Palermo, V.le delle Scienze Building 6, 90128 Palermo, Italy.
Institute of Anatomy and Cell Biology, Paracelsus Medical University, Nuremberg and Salzburg, Prof. Ernst Nathan Str. 1, 90419 Nuremberg, Germany.
Polymers (Basel). 2024 Jan 25;16(3):331. doi: 10.3390/polym16030331.
Bilayer scaffolds could provide a suitable topology for osteochondral defect repair mimicking cartilage and subchondral bone architecture. Hence, they could facilitate the chondro- and osteogenic lineage commitment of multipotent mesenchymal stromal cells (MSCs) with hydroxyapatite, the major inorganic component of bone, stimulating osteogenesis. Highly porous poly-L-lactic acid (PLLA) scaffolds with two layers of different pore sizes (100 and 250 µm) and hydroxyapatite (HA) supplementation were established by thermally induced phase separation (TIPS) to study growth and osteogenesis of human (h) MSCs. The topology of the scaffold prepared via TIPS was characterized using scanning electron microscopy (SEM), a microCT scan, pycnometry and gravimetric analysis. HMSCs and porcine articular chondrocytes (pACs) were seeded on the PLLA scaffolds without/with 5% HA for 1 and 7 days, and the cell attachment, survival, morphology, proliferation and gene expression of cartilage- and bone-related markers as well as sulfated glycosaminoglycan (sGAG) synthesis were monitored. All scaffold variants were cytocompatible, and hMSCs survived for the whole culture period. Cross-sections revealed living cells that also colonized inner scaffold areas, producing an extracellular matrix (ECM) containing sGAGs. The gene expression of cartilage and bone markers could be detected. HA represents a cytocompatible supplement in PLLA composite scaffolds intended for osteochondral defects.
双层支架可为模仿软骨和软骨下骨结构的骨软骨缺损修复提供合适的拓扑结构。因此,它们可以促进多能间充质基质细胞(MSCs)向软骨和成骨谱系分化,其中骨的主要无机成分羟基磷灰石可刺激成骨。通过热诱导相分离(TIPS)制备了具有两层不同孔径(100和250 µm)且添加了羟基磷灰石(HA)的高度多孔聚-L-乳酸(PLLA)支架,以研究人(h)MSCs的生长和成骨情况。通过扫描电子显微镜(SEM)、显微CT扫描、液体比重计法和重量分析对通过TIPS制备的支架拓扑结构进行了表征。将hMSCs和猪关节软骨细胞(pACs)接种在不含/含5% HA的PLLA支架上培养1天和7天,监测细胞附着、存活、形态、增殖以及软骨和骨相关标志物的基因表达以及硫酸化糖胺聚糖(sGAG)的合成。所有支架变体均具有细胞相容性,hMSCs在整个培养期内存活。横截面显示活细胞也在支架内部区域定植,产生含有sGAGs的细胞外基质(ECM)。可检测到软骨和骨标志物的基因表达。HA是用于骨软骨缺损的PLLA复合支架中的一种细胞相容性补充剂。