Transplantation of human iPSC-derived muscle stem cells in the diaphragm of Duchenne muscular dystrophy model mice.
Yasutomo MiuraMase SatoToshie KuwaharaTomoki EbataYasuhiko TabataHidetoshi SakuraiPublished in: PloS one (2022)
Duchenne muscular dystrophy (DMD) is an intractable genetic muscular disorder characterized by the loss of DYSTROPHIN. The restoration of DYSTROPHIN is expected to be a curative therapy for DMD. Because muscle stem cells (MuSCs) can regenerate damaged myofibers with full-length DYSTROPHIN in vivo, their transplantation is being explored as such a therapy. As for the transplanted cells, primary satellite cells have been considered, but donor shortage limits their clinical application. We previously developed a protocol that differentiates induced pluripotent stem cells (iPSCs) to MuSCs (iMuSCs). To ameliorate the respiratory function of DMD patients, cell transplantation to the diaphragm is necessary but difficult, because the diaphragm is thin and rapidly moves. In the present study, we explored the transplantation of iMuSCs into the diaphragm. First, we show direct cell injection into the diaphragm of mouse was feasible. Then, to enhance the engraftment of the transplanted cells in a rapidly moving diaphragm, we mixed polymer solutions of hyaluronic acid, alginate and gelatin to the cell suspension, finding a solution of 20% dissolved hyaluronic acid and 80% dissolved gelatin improved the engraftment. Thus, we established a method for cell transplantation into mouse diaphragm and show that an injectable hyaluronic acid-gelatin solution enables the engraftment of iMuSCs in the diaphragm.
Keyphrases
- duchenne muscular dystrophy
- hyaluronic acid
- cell therapy
- mechanical ventilation
- stem cells
- induced pluripotent stem cells
- induced apoptosis
- muscular dystrophy
- single cell
- cell cycle arrest
- skeletal muscle
- randomized controlled trial
- acute respiratory distress syndrome
- endothelial cells
- mesenchymal stem cells
- ejection fraction
- newly diagnosed
- endoplasmic reticulum stress
- end stage renal disease
- gene expression
- intensive care unit
- body composition
- genome wide
- high intensity
- patient reported outcomes
- resistance training
- replacement therapy
- wound healing
- patient reported
- high fat diet induced