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Reilly, G. C.

Publications and source records attributed to Reilly, G. C..

2 recordsLinked to original sources

Angiogenic PolyHIPE Scaffolds Decorated with Extracellular Matrix as Periosteum Substitutes

1.The periosteum is the connective tissue that envelopes bone and contributes to the normal bone healing process. Periosteal grafts have shown excellent success in the treatment of nonunion bone defects but surgical challenges such as donor site morbidity and graft availability have limited their clinical use. Artificial periosteal membranes are being explored as off-the-shelf alternatives, with several groups investigating the use of decellularized tissues or extracellular matrix (ECM)-based strategies for this purpose. In this study, we investigate the use of in vitro-generated, fibroblast-derived ECM to decorate porous biodegradable scaffolds for use as synthetic periosteal grafts. Scaffolds were fabricated using an emulsion templating technique from a blend of polycaprolactone methacrylate (PCL-M) and poly(glycerol sebacate) methacrylate (PGS-M), resulting in membranes with large, interconnected pores (average pore size = 49.6 {+/-} 40.9 {micro}m, average window size = 12.6 {+/-} 6.1 {micro}m) and structural characteristics suitable for soft tissue applications. The BJ5ta fibroblast cell line was cultured on scaffolds for 14 days to deposit ECM, after which constructs were decellularized. When tested in vitro, periosteal-typical cells exhibited a significantly higher growth rate on ECM-decorated scaffolds compared to controls. Additionally, the chick chorioallantoic membrane (CAM) demonstrated that ECM decoration had a positive angiogenic effect. This proof-of-concept study highlights a promising approach to enhance the biological properties of synthetic membranes, while avoiding challenges associated with decellularizing whole tissues.

bioengineering↗

A multi-structural finite element model to simulate atomic force microscopy nanoindentation of single cells

Single cell mechanical properties represent an increasingly studied descriptor for health and disease. Atomic force microscopy (AFM) has been widely used to measure single cell stiffness, despite its experimental limitations. The development of a computational framework to simulate AFM nanoindentation experiments could be a valuable tool to complement experimental findings. A single cell multi-structural finite element model was designed to this aim by using confocal images of bone cells, comprised of the cell nucleus, cytoplasm and actin cytoskeleton. The computational cell stiffness values were in the range of experimental values acquired on the same cells for nanoindentation of the cell nucleus and periphery, despite showing higher stiffness for the nucleus than for the periphery, oppositely to the average experimental findings. These results suggest it would be of interest to model different single cells with known experimental effective moduli to evaluate the ability of the computational models to replicate experimental results.

bioengineering↗