The Phenotype of Mesenchymal Stromal Cell and Articular Chondrocyte Cocultures on Highly Porous Bilayer Poly-L-Lactic Acid Scaffolds Produced by Thermally Induced Phase Separation and Supplemented with Hydroxyapatite.
Wally FerraroAurelio CivilleriClemens GögeleCamilla CarboneIlenia VitranoFrancesco Carfì PaviaValerio Maria Bartolo BrucatoVincenzo La CarrubbaChristian WernerKerstin Schäfer-EckartGundula Gesine Schulze-TanzilPublished in: Polymers (2024)
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.
Keyphrases
- tissue engineering
- extracellular matrix
- lactic acid
- gene expression
- bone regeneration
- bone marrow
- single cell
- bone mineral density
- mesenchymal stem cells
- electron microscopy
- living cells
- bone loss
- high glucose
- endothelial cells
- soft tissue
- diabetic rats
- dna methylation
- stem cells
- cell therapy
- signaling pathway
- computed tomography
- umbilical cord
- magnetic resonance imaging
- drug induced
- oxidative stress
- single molecule
- magnetic resonance
- copy number
- mass spectrometry
- induced pluripotent stem cells