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What are the potential applications and limitations of using MC3T3-E1 and hMSC in regenerative medicine and tissue engineering? 


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MC3T3-E1 cells and human mesenchymal stem cells (hMSCs) hold significant promise in regenerative medicine and tissue engineering. MC3T3-E1 cells, when encapsulated with extracellular vesicles (EVs) in a 3D hydrogel system, exhibit enhanced osteogenic responses, making them valuable for bone tissue engineering. On the other hand, hMSCs, due to their self-renewal and immunomodulatory potential, are promising for clinical therapy, but unmodified hMSCs face challenges like low therapeutic potential and immunocompatibility issues. Strategies like modifying hMSCs with soluble factors, genetic methods, and 3D culture techniques have been explored to enhance their potency and functionality for clinical applications. While MC3T3-E1 cells show quick multiplication and moderate cell number increment in response to nanochitosan blends, hMSCs require modifications to overcome limitations for effective regenerative medicine applications.

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MC3T3-E1-derived extracellular vesicles show osteoinductive potential in a 3D hydrogel model, offering a cell-free approach for enhanced bone regeneration in tissue engineering, overcoming limitations of cell-based therapies.
MC3T3-E1 cells offer osteogenic differentiation potential for bone tissue engineering, while hMSCs provide versatility for various tissue types. Limitations include potential cytotoxicity at higher nanoparticle concentrations.
MC3T3-E1 cells showed compatibility with nanochitosan/polyvinylpyrrolidone blends, indicating potential for bone tissue engineering. Limitations and comparison with hMSC were not addressed in the paper.
Not addressed in the paper.

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