Once they were able to isolate skeletal muscle cells using the newly identified surface markers, the research team matured those cells in the lab to
create dystrophin - producing muscle fibers.
Not exact matches
The result was the largest deletion ever observed in the
dystrophin gene using CRISPR / Cas9, and the study was the first to
create corrected human iPS cells that could directly restore functional muscle tissue affected by Duchenne.
Children with DMD have a mutation that cripples the body's ability to produce a protein called
dystrophin, which helps absorb the shock or energy that's
created when a muscle contracts.
Using the natural human development process as a guide, the researchers developed ways to mature muscle cells in the laboratory to
create muscle fibers that restore
dystrophin, the protein that is missing in the muscles of boys with Duchenne.
«This is the first study to demonstrate that functional muscle cells can be
created in a laboratory and restore
dystrophin in animal models of Duchenne using the human development process as a guide.»