Definition of a Novel Plasmid-Based Gene Transfection Protocol of Mammalian Skeletal Muscles by Means of In Vivo Electroporation.
Enrico P SpugniniScimeca ManuelBruno AmadioGiancarlo CorteseMaurizio FanciulliBruno VincenziAntonio De LucaAlfonso BaldiPublished in: International journal of molecular sciences (2020)
We describe an original electroporation protocol for in vivo plasmid DNA transfection. The right hind limbs of C57 mice are exposed to a specifically designed train of permeabilizing electric pulses by transcutaneous application of tailored needle electrodes, immediately after the injection of pEGFP-C1 plasmid encoding GFP (Green Fluorescente Protein). The electroporated rodents show a greater GFP expression than the controls at three different time points (4, 10, and 15 days). The electroporated muscles display only mild interstitial myositis, with a significant increase in inflammatory cell infiltrates. Finally, mild gait abnormalities are registered in electroporated mice only in the first 48 h after the treatment. This protocol has proven to be highly efficient in terms of expression levels of the construct, is easy to apply since it does not require surgical exposure of the muscle and is well tolerated by the animals because it does not cause evident morphological and functional damage to the electroporated muscle.
Keyphrases
- highly efficient
- escherichia coli
- poor prognosis
- randomized controlled trial
- crispr cas
- skeletal muscle
- high fat diet induced
- oxidative stress
- binding protein
- ultrasound guided
- single cell
- cell therapy
- circulating tumor
- type diabetes
- gene expression
- stem cells
- cell free
- mesenchymal stem cells
- dna methylation
- high resolution
- rheumatoid arthritis
- mass spectrometry
- metabolic syndrome
- bone marrow
- solid state
- circulating tumor cells