Background: Bone morphogenetic protein-2 () has a high potential to induce bone tissue formation in skeletal muscles. We developed a bone induction system in skeletal muscles using the gene through in vivo electroporation. Natural bone tissues with skeletal muscles can be considered potential candidates for biomaterials. However, our previous system using plate-type electrodes did not achieve a 100% success rate in inducing bone tissues in skeletal muscles. In this study, we aimed to enhance the efficiency of bone tissue formation in skeletal muscles by using a non-viral gene expression plasmid vector (pCAGGS-) and needle-type electrodes.
Methods: We injected the gene with pCAGGS- into the skeletal muscles of rats' legs and immediately placed needle-type electrodes there. Skeletal tissues were then observed on the 21st day after gene transfer using soft X-ray and histological analyses.
Results: The use of needle-type electrodes resulted in a 100% success rate in inducing bone tissues in skeletal muscles. In contrast, the plate-type electrodes only exhibited a 33% success rate. Thus, needle-type electrodes can be more efficient and reliable for transferring the gene to skeletal muscles, making them potential biomaterials for repairing bone defects.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10890310 | PMC |
http://dx.doi.org/10.3390/ma17040880 | DOI Listing |
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