In Vitro and In Vivo Biocompatibility Assessment of a Thermosensitive Injectable Chitosan-Based Hydrogel for Musculoskeletal Tissue Engineering.
Barbara CancianiFrancesca SemeraroValentina Rafaela Herrera MillarFrancesca GervasoAlessandro PoliniAntonella StanzioneGiuseppe Michele PerettiAlessia Di GiancamilloLaura MangiaviniPublished in: International journal of molecular sciences (2023)
Musculoskeletal impairments, especially cartilage and meniscus lesions, are some of the major contributors to disabilities. Thus, novel tissue engineering strategies are being developed to overcome these issues. In this study, the aim was to investigate the biocompatibility, in vitro and in vivo, of a thermosensitive, injectable chitosan-based hydrogel loaded with three different primary mesenchymal stromal cells. The cell types were human adipose-derived mesenchymal stromal cells (hASCs), human bone marrow stem cells (hBMSCs), and neonatal porcine infrapatellar fat-derived cells (IFPCs). For the in vitro study, the cells were encapsulated in sol-phase hydrogel, and then, analyzed via live/dead assay at 1, 4, 7, and 14 days to compare their capacity to survive in the hydrogel. To assess biocompatibility in vivo, cellularized scaffolds were subcutaneously implanted in the dorsal pouches of nude mice and analyzed at 4 and 12 weeks. Our data showed that all the different cell types survived (the live cell percentages were between 60 and 80 at all time points in vitro) and proliferated in the hydrogel (from very few at 4 weeks to up to 30% at 12 weeks in vivo); moreover, the cell-laden hydrogels did not trigger an immune response in vivo. Hence, our hydrogel formulation showed a favorable profile in terms of safety and biocompatibility, and it may be applied in tissue engineering strategies for cartilage and meniscus repair.
Keyphrases
- tissue engineering
- bone marrow
- drug delivery
- stem cells
- single cell
- cell therapy
- induced apoptosis
- immune response
- endothelial cells
- wound healing
- cell cycle arrest
- spinal cord
- adipose tissue
- mesenchymal stem cells
- cancer therapy
- induced pluripotent stem cells
- hyaluronic acid
- spinal cord injury
- high throughput
- inflammatory response
- skeletal muscle
- machine learning
- oxidative stress
- neuropathic pain
- metabolic syndrome
- electronic health record
- artificial intelligence
- endoplasmic reticulum stress
- high fat diet induced