Human Osteoblasts’ Response to Biomaterials for Subchondral Bone Regeneration in Standard and Aggressive Environments

• Published in: International journal of molecular sciences Vol. 24; no. 19; p. 14764
• Main Authors: Pagani, Stefania, Salerno, Manuela, Filardo, Giuseppe, Locs, Janis, van Osch, Gerjo J.V.M, Vecstaudza, Jana, Dolcini, Laura, Borsari, Veronica, Fini, Milena, Giavaresi, Gianluca, Columbaro, Marta
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.10.2023; MDPI
• Subjects: Aging; Arthritis; Biological products; Biomedical materials; biomimetic scaffold; Cartilage; Cells; Collagen; Exercise; Gene expression; human osteoblasts; Hydroxyapatite; Joint replacement surgery; Metabolism; Metabolites; Morphology; Older people; Osteoarthritis; osteochondral regeneration; oxidative stress; Physical fitness; Netherlands
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms241914764

Osteochondral lesions, when not properly treated, may evolve into osteoarthritis (OA), especially in the elderly population, where altered joint function and quality are usual. To date, a collagen/collagen–magnesium–hydroxyapatite (Col/Col-Mg-HAp) scaffold (OC) has demonstrated good clinical results, although suboptimal subchondral bone regeneration still limits its efficacy. This study was aimed at evaluating the in vitro osteogenic potential of this scaffold, functionalized with two different strategies: the addition of Bone Morphogenetic Protein-2 (BMP-2) and the incorporation of strontium (Sr)-ion-enriched amorphous calcium phosphate (Sr-ACP) granules. Human osteoblasts were seeded on the functionalized scaffolds (OC+BMP-2 and OC+Sr-ACP, compared to OC) under stress conditions reproduced with the addition of H2O2 to the culture system, as well as in normal conditions, and evaluated in terms of morphology, metabolic activity, gene expression, and matrix synthesis. The OC+BMP-2 scaffold supported a better osteoblast morphology and stimulated scaffold colonization, cell activity, and extracellular matrix secretion, especially in the stressed culture environment but also in normal culture conditions, with increased expression of genes related to osteoblast differentiation. In conclusion, the incorporation of BMP-2 into the Col/Col-Mg-HAp scaffold also represents an improvement of the osteochondral scaffold in more challenging conditions, supporting further preclinical studies to optimize it for use in clinical practice.