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The microRNA miR‐133b functions to slow Duchenne muscular dystrophy pathogenesis
Author(s) -
Taetzsch Thomas,
Shapiro Dillon,
Eldosougi Randa,
Myers Tracey,
Settlage Robert E.,
Valdez Gregorio
Publication year - 2020
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jp280405
Subject(s) - duchenne muscular dystrophy , skeletal muscle , biology , regeneration (biology) , muscular dystrophy , itga7 , myocyte , microbiology and biotechnology , microrna , mdx mouse , stem cell , endocrinology , dystrophin , genetics , gene
Key points Impairment of muscle biogenesis contributes to the progression of Duchenne muscular dystrophy (DMD). As a muscle enriched microRNA that has been implicated in muscle biogenesis, the role of miR‐133b in DMD remains unknown. To assess miR‐133b function in DMD‐affected skeletal muscles, we genetically ablated miR‐133b in the mdx mouse model of DMD. We show that deletion of miR‐133b exacerbates the dystrophic phenotype of DMD‐afflicted skeletal muscle by dysregulating muscle stem cells involved in muscle biogenesis, in addition to affecting signalling pathways related to inflammation and fibrosis. Our results provide evidence that miR‐133b may underlie DMD pathology by affecting the proliferation and differentiation of muscle stem cells.Abstract Duchenne muscular dystrophy (DMD) is characterized by progressive skeletal muscle degeneration. No treatments are currently available to prevent the disease. While the muscle enriched microRNA miR‐133b has been implicated in muscle biogenesis, its role in DMD remains unknown. To assess miR‐133b function in DMD‐affected skeletal muscles, we genetically ablated miR‐133b in the mdx mouse model of DMD. In the absence of miR‐133b, the tibialis anterior muscle of P30 mdx mice is smaller in size and exhibits a thickened interstitial space containing more mononucleated cells. Additional analysis revealed that miR‐133b deletion influences muscle fibre regeneration, satellite cell proliferation and differentiation, and induces widespread transcriptomic changes in mdx muscle. These include known miR‐133b targets as well as genes involved in cell proliferation and fibrosis. Altogether, our data demonstrate that skeletal muscles utilize miR‐133b to mitigate the deleterious effects of DMD.