| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2130092 | Experimental Cell Research | 2015 | 9 Pages |
•We have described a step by step guide for femoral artery perfusion in mouse.•Intra-femoral artery canulation in mice provides efficient hind limb skeletal muscle perfusion.•This method can be used for evaluation of gene delivery vectors or stem cells into muscle.•Human iPS-derived myogenic progenitors are able to seed into skeletal muscles and engraft following intra-femoral artery perfusion in a mouse model for Duchenne muscular dystrophy (DMD).
Muscular dystrophies are among major inherited muscle disorders characterized by progressive muscle damage and fibrosis with no definitive cure. Recently, gene or cell based therapies have been developed to restore the missing gene expression or replace the damaged tissues. In order to test the efficiency of these therapies in mice models of muscular dystrophies, the arterial route of delivery is very advantageous as it provides uniform muscle exposure to the therapeutic agents or cells. Although there are few reports of arterial delivery of the therapeutic agents or cells in mice, there is no in-depth description and evaluation of its efficacy in perfusion of downstream muscles. This study is aimed to develop a practical method for intra-femoral artery perfusion in mice and to evaluate perfusion efficiency using near-infrared-fluorescence (NIRF) imaging as well as histology following stem cell delivery.Our results provide a practical guide to perform this delicate method in mice. By using a sensitive fluorescent dye, different muscle groups of the hindlimb have been evaluated for proper perfusion. As the final step, we have validated the efficiency of arterial cell delivery into muscles using human iPS-derived myogenic cells in an immunodeficient mouse model for Duchenne muscular dystrophy (NSG-mdx4cv).
