[HTML][HTML] Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy
DU Kemaladewi, WMH Hoogaars… - BMC medical …, 2011 - Springer
DU Kemaladewi, WMH Hoogaars, SH van Heiningen, S Terlouw, DJJ de Gorter…
BMC medical genomics, 2011•SpringerBackground Myostatin is a potent muscle growth inhibitor that belongs to the Transforming
Growth Factor-β (TGF-β) family. Mutations leading to non functional myostatin have been
associated with hypermuscularity in several organisms. By contrast, Duchenne muscular
dystrophy (DMD) is characterized by a loss of muscle fibers and impaired regeneration. In
this study, we aim to knockdown myostatin by means of exon skipping, a technique which
has been successfully applied to reframe the genetic defect of dystrophin gene in DMD …
Growth Factor-β (TGF-β) family. Mutations leading to non functional myostatin have been
associated with hypermuscularity in several organisms. By contrast, Duchenne muscular
dystrophy (DMD) is characterized by a loss of muscle fibers and impaired regeneration. In
this study, we aim to knockdown myostatin by means of exon skipping, a technique which
has been successfully applied to reframe the genetic defect of dystrophin gene in DMD …
Background
Myostatin is a potent muscle growth inhibitor that belongs to the Transforming Growth Factor-β (TGF-β) family. Mutations leading to non functional myostatin have been associated with hypermuscularity in several organisms. By contrast, Duchenne muscular dystrophy (DMD) is characterized by a loss of muscle fibers and impaired regeneration. In this study, we aim to knockdown myostatin by means of exon skipping, a technique which has been successfully applied to reframe the genetic defect of dystrophin gene in DMD patients.
Methods
We targeted myostatin exon 2 using antisense oligonucleotides (AON) in healthy and DMD-derived myotubes cultures. We assessed the exon skipping level, transcriptional expression of myostatin and its target genes, and combined myostatin and several dystrophin AONs. These AONs were also applied in the mdx mice models via intramuscular injections.
Results
Myostatin AON induced exon 2 skipping in cell cultures and to a lower extent in the mdx mice. It was accompanied by decrease in myostatin mRNA and enhanced MYOG and MYF5 expression. Furthermore, combination of myostatin and dystrophin AONs induced simultaneous skipping of both genes.
Conclusions
We conclude that two AONs can be used to target two different genes, MSTN and DMD, in a straightforward manner. Targeting multiple ligands of TGF-beta family will be more promising as adjuvant therapies for DMD.
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