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Absence of microRNA-21 does not reduce muscular dystrophy in mouse models of LAMA2-CMD
Bernardo Moreira Soares Oliveira1, Madeleine Durbeej1, Johan Holmberg1
1Muscle Biology Unit, Department of Experimental Medical Science, Lund University, Lund, Sweden.
Abstract:
MicroRNAs (miRNAs) are short non-coding RNAs that modulate gene expression post-transcriptionally. Current evidence suggests that miR-21 plays a significant role in the progression of fibrosis in muscle diseases. Laminin-deficient congenital muscular dystrophy (LAMA2-CMD) is a severe form of congenital muscular dystrophy caused by mutations in the gene encoding laminin α2 chain. Mouse models dy3K/dy3K and dy2J/dy2J, respectively, adequately mirror severe and milder forms of LAMA2-CMD. Both human and mouse LAMA2-CMD muscles are characterized by extensive fibrosis and considering that fibrosis is the final step that destroys muscle during the disease course, anti-fibrotic therapies may be effective strategies for prevention of LAMA2-CMD. We have previously demonstrated a significant up-regulation of the pro-fibrotic miR-21 in dy3K/dy3K and dy2J/dy2J skeletal muscle. Hence, the objective of this study was to explore if absence of miR-21 reduces fibrogenesis and improves the phenotype of LAMA2-CMD mice. Thus, we generated dy3K/dy3K and dy2J/dy2J mice devoid of miR-21 (dy3K/miR-21 and dy2J/miR-21 mice, respectively). However, the muscular dystrophy phenotype of dy3K/miR-21 and dy2J/miR-21 double knock-out mice was not improved compared to dy3K/dy3K or dy2J/dy2J mice, respectively. Mice displayed the same body weight, dystrophic muscles (with fibrosis) and impaired muscle function. These data indicate that miR-21 may not be involved in the development of fibrosis in LAMA2-CMD.
Insights
MicroRNA-21 (miR-21) does not appear to drive fibrosis in laminin-deficient congenital muscular dystrophy (LAMA2-CMD). Eliminating miR-21 in mouse models did not improve muscle fibrosis or disease symptoms.
Area of Science:
- Molecular Biology
- Genetics
- Biochemistry
Background:
- MicroRNAs (miRNAs) are key regulators of gene expression.
- Fibrosis is a major pathological feature in laminin-deficient congenital muscular dystrophy (LAMA2-CMD).
- Previous studies indicated a potential role for miR-21 in promoting fibrosis in LAMA2-CMD.
Purpose of the Study:
- To investigate the role of miR-21 in the development of fibrosis in LAMA2-CMD.
- To determine if the absence of miR-21 could ameliorate the disease phenotype in LAMA2-CMD mouse models.
Main Methods:
- Generated double knockout mice by crossing LAMA2-CMD mouse models (dy3K/dy3K and dy2J/dy2J) with miR-21 knockout mice.
- Assessed muscle fibrosis, body weight, and muscle function in the resulting double knockout mice (dy3K/miR-21 and dy2J/miR-21) compared to their respective LAMA2-CMD counterparts.
Main Results:
- Absence of miR-21 did not improve the muscular dystrophy phenotype in LAMA2-CMD mice.
- Double knockout mice exhibited similar body weight, muscle fibrosis, and impaired muscle function compared to LAMA2-CMD mice without miR-21 deficiency.
- These findings suggest miR-21 is not involved in LAMA2-CMD fibrosis development.
Conclusions:
- miR-21 does not appear to play a significant role in the pathogenesis of fibrosis in LAMA2-CMD.
- Targeting miR-21 may not be an effective therapeutic strategy for LAMA2-CMD-associated fibrosis.
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