Morpholino treatment improves muscle function and pathology of Pitx1 transgenic mice.

Abstract

Paired-like homeodomain transcription factor 1 (PITX1) was proposed to be part of the disease mechanisms of facioscapulohumeral muscular dystrophy (FSHD). We generated a tet-repressible muscle-specific Pitx1 transgenic mouse model which develops phenotypes of muscular dystrophy after the PITX1 expression is induced. In this study, we attempted to block the translation of PITX1 protein using morpholinos. Three groups of the transgenic mice received intravenous injections of phosphorodiamidate morpholino oligomers (PMO) (100 mg/kg), octaguanidinium dendrimer-conjugated morpholino (vivo-morpholino) (10 mg/kg), or phosphate-buffered saline (PBS) after the PITX1 expression was induced. Immunoblotting data showed that PITX1 expression in the triceps and quadriceps was significantly reduced 70% and 63% by the vivo-morpholino treatment, respectively. Muscle pathology of the mice treated with the vivo-morpholino was improved by showing 44% fewer angular-shaped atrophic myofibers. Muscle function determined by grip strength was significantly improved by the vivo-morpholino treatment. The study showed that systemic delivery of the vivo-morpholino reduced the PITX1 expression and improved the muscle phenotypes. Aberrant expression of DUX4 from the last unit of the D4Z4 array has been proposed to be the cause of FSHD. The findings of this study suggest that the same principle may be applied to suppress the aberrantly expressed DUX4 in FSHD.

• Authors: Sachchida Nand Pandey, Yi-Chien Lee, Toshifumi Yokota, Yi-Wen Chen
• Journal: Molecular therapy : the journal of the American Society of Gene Therapy (Mol Ther) Vol. 22 Issue 2 Pg. 390-396 (Feb 2014) ISSN: 1525-0024 [Electronic] United States
• PMID: 24232919 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.)

Chemical References

• Morpholinos
• Paired Box Transcription Factors
• homeobox protein PITX1

Topics

• Animals
• Disease Models, Animal
• Female
• Gene Expression Regulation
• Male
• Mice
• Mice, Transgenic
• Morpholinos (administration & dosage, adverse effects, genetics)
• Muscle Strength (drug effects, genetics)
• Muscle, Skeletal (drug effects, metabolism, pathology)
• Muscular Dystrophy, Facioscapulohumeral (genetics, rehabilitation, therapy)
• Paired Box Transcription Factors (genetics, metabolism)