BackgroundSkeletal muscle tissue engineering often involves the prefabrication of muscle tissues in vitro by differentiation and maturation of muscle precursor cells on a platform which provides an environment that facilitates the myogenic differentiation of the seeded cells.MethodsPoly lactic-co-glycolic acid (PLGA) 3D printed scaffolds, which simulate the highly complex structure of extracellular matrix (ECM), were fabricated by E-jet 3D printing in this study. The scaffolds were used as platforms, providing environment that aids in growth, differentiation and other properties of C2C12 myoblast cells.ResultsThe C2C12 myoblast cells grown on the PLGA 3D printed platforms had enhanced cell adhesion and proliferation. Moreover, the platforms were able to induce myogenic differentiation of the myoblast cells by promoting the formation of myotubes and up-regulating the expressions of myogenic genes (MyHC and MyOG).ConclusionThe fabricated 3D printed platforms have excellent biocompatibility, thereby can potentially be used as functional cell culture platforms in skeletal tissue engineering and regeneration.
Exposing wounds to pulsed radiofrequency accelerated wound healing in this diabetic mouse model by means of significantly increasing dermal cell proliferation and collagen synthesis. A cellular mechanism behind these observations has been proposed.
With the growing therapeutic importance of cell microcarriers, there has been a rise in the need to develop technologies that facilitate efficient microencapsulation of cells, currently limited by a lack of straightforward and low‐cost strategies for single‐cell isolation and printing. Thus, the aim of this study is to develop a gentle and cell‐compatible electro‐hydrodynamic jet 3D printing technique to facilitate the efficient microencapsulation of cells in hydrogel microspheres, and investigate the effects of parameters (flow rate, voltage frequency, nozzle diameter, working distance, and substrate velocity) on the printing process. Stable microspheres are obtained by regulating these parameters to balance various forces, with control of their diameters in the range of 100–600 µm. The study demonstrates that under optimized conditions, the technique is able to successfully encapsulate cells within hydrogel microspheres with high viability over a wide range of diameters. This 3D printing technique expands the potential utility of microspheres into additional biological applications, such as cancer biology and drug screening. It can also be used as an effective platform for the production of tumor spheroids, generating multicellular spheroid models in vitro or for injectable cell delivery.
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