Bone tissue engineering as an alternative strategy, provides a great opportunity for regeneration of large bone tissue lesions. The use of biodegradable porous scaffolds along with stem cells, cytokines and growth factors improves cell survival, adhesion, proliferation and differentiation. In the present study, clay nanoplates (CNPs) were surface-modified (MCNPs) using phosphoric acid and calcium hydroxide, then porous polyurethane (PU) scaffolds and PU-MCNPs nanocomposite scaffolds were synthesized using solvent evaporation-dissolution technique. Physicochemical and morphological properties of scaffolds and MCNPs were studied by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and scanning electron microscopy (SEM). Moreover, thermal behavior of scaffolds was assessed by differential scanning calorimetry (DSC). Degradability, water uptake and mechanical behaviors of scaffolds were evaluated and hydrophilicity properties of them were obtained by contact angle technique. MTT assay and Acridine Orange/Ethidium Bromide (AO/EB) staining were used to assess the biocompatibility of MCNPs and PU scaffolds regarding cell attachment and proliferation support. Osteogenic differentiation of cultured human adipose derived mesenchymal stem cells (hADSCs) on MCNPs, PU and PU-MCNPs scaffolds was evaluated using common osteogenic markers such as alkaline phosphatase (ALP) activity, calcium content assay, Alizarin Red staining, immunocytochemical analysis (ICC) and quantitative real-time PCR (qPCR). According to the results, the surface modification of CNPs and their presence into the PU scaffolds significantly enhanced proliferation and osteogenic differentiation of hADSCs. These results were obtained by higher ALP enzyme activity, biomineralization and expression of osteogenic related proteins and genes in differentiated hADSCs on PU-MCNPs scaffolds. In conclusion, our results revealed that these biocompatible nanocomposites porous scaffolds with proper cell adhesion and proliferation as well as effective osteogenic differentiation and which are able to provide a new and useful matrix for bone tissue engineering purposes.
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http://dx.doi.org/10.1016/j.msec.2019.109857 | DOI Listing |
Biochem Biophys Res Commun
January 2025
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration & National Clinical Research Center for Oral Diseases & Shaanxi International Joint Research Center for Oral Diseases, Center for Tissue Engineering, School of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi, 710032, China; Department of Orthodontics, School of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi, 710032, China. Electronic address:
Periodontal disease is a major contributor to tooth loss worldwide in adults. Particularly, periodontal bone defect is a common clinical condition, yet current therapeutic strategies exhibit limited effectiveness. Recently, natural bone graft materials have attracted considerable interest for enhancing bone defect repair due to their superior biocompatibility and osteogenic capabilities.
View Article and Find Full Text PDFRegulatory T cells (Tregs) are increasingly being recognized for their role in promoting tissue repair. In this issue of the JCI, Chen et al. found that Tregs at the site of bone injury contribute to bone repair.
View Article and Find Full Text PDFElife
January 2025
Center for Medical Genetics Ghent, Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Heritable fragile bone disorders (FBDs), ranging from multifactorial to rare monogenic conditions, are characterized by an elevated fracture risk. Validating causative genes and understanding their mechanisms remain challenging. We assessed a semi-high throughput zebrafish screening platform for rapid in vivo functional testing of candidate FBD genes.
View Article and Find Full Text PDFArterioscler Thromb Vasc Biol
January 2025
British Heart Foundation Centre of Research Excellence, School of Cardiovascular and Metabolic Medicine & Sciences, King's College London, United Kingdom. (M.W., M.F., R.O., L.S., M.M., C.M.S.).
Background: The ECM (extracellular matrix) provides the microenvironmental niche sensed by resident vascular smooth muscle cells (VSMCs). Aging and disease are associated with dramatic changes in ECM composition and properties; however, their impact on the VSMC phenotype remains poorly studied.
Methods: Here, we describe a novel in vitro model system that utilizes endogenous ECM to study how modifications associated with age and metabolic disease impact the VSMC phenotype.
RSC Adv
January 2025
School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University, Shandong Key Laboratory of Oral Tissue Regeneration, Shandong Engineering Research Center of Dental Materials and Oral Tissue Regeneratioon, Shandong Provincial Clinical Research Center for Oral Diseases Ji'nan 250012 China
Bone defects represent a significant challenge in clinical practice, driving the need for innovative solutions that effectively support bone regeneration. Barrier membranes, due to playing a critical role in creating an environment conducive to bone regeneration by preventing the infiltration of non-osteogenic tissues, are widely applied to bone repair. However, inadequate spatial stability and osteogenesis-promoting ability often limit current barrier membranes.
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