Key result
Fibrillin-2 loss in mice reduces muscle mass ~28% and increases fat via activated BMP signaling.
Why the study?
Does genetic ablation of Fbn2 cause myopathy and abnormal BMP signaling in mice?
Does genetic ablation of Fbn2 cause myopathy and abnormal BMP signaling in mice?
Effect estimate: 28% reduction
p-value: p=0.001
Loss of fibrillin-2 causes congenital myopathy in mice via abnormal activation of BMP signaling, suggesting FBN2 as a candidate gene for recessive congenital muscular dystrophy.
FBN2 variants merit screening in congenital myopathy cohorts; leaves open human translation and therapeutic targeting.
Fibrillins are large extracellular macromolecules that polymerize to form the backbone structure of connective tissue microfibrils. Mutations in the gene for fibrillin-1 cause the Marfan syndrome, while mutations in the gene for fibrillin-2 cause Congenital Contractural Arachnodactyly. Both are autosomal dominant disorders, and both disorders affect musculoskeletal tissues. Here we show that Fbn2 null mice (on a 129/Sv background) are born with reduced muscle mass, abnormal muscle histology, and signs of activated BMP signaling in skeletal muscle. A delay in Myosin Heavy Chain 8, a perinatal myosin, was found in Fbn2 null forelimb muscle tissue, consistent with the notion that muscle defects underlie forelimb contractures in these mice. In addition, white fat accumulated in the forelimbs during the early postnatal period. Adult Fbn2 null mice are already known to demonstrate persistent muscle weakness. Here we measured elevated creatine kinase levels in adult Fbn2 null mice, indicating ongoing cycles of muscle injury. On a C57Bl/6 background, Fbn2 null mice showed severe defects in musculature, leading to neonatal death from respiratory failure. These new findings demonstrate that loss of fibrillin-2 results in phenotypes similar to those found in congenital muscular dystrophies and that FBN2 should be considered as a candidate gene for recessive congenital muscular dystrophy. Both in vivo and in vitro evidence associated muscle abnormalities and accumulation of white fat in Fbn2 null mice with abnormally activated BMP signaling. Genetic rescue of reduced muscle mass and accumulation of white fat in Fbn2 null mice was accomplished by deleting a single allele of Bmp7. In contrast to other reports that activated BMP signaling leads to muscle hypertrophy, our findings demonstrate the exquisite sensitivity of BMP signaling to the fibrillin-2 extracellular environment during early postnatal muscle development. New evidence presented here suggests that fibrillin-2 can sequester BMP complexes in a latent state.
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Sengle et al. (2015) studied Myopathy. Fbn2 null mutation vs. Wildtype mice was evaluated on Total forearm muscle mass (28% reduction, p=0.001). Loss of fibrillin-2 in mice causes reduced muscle mass, abnormal muscle histology, and accumulation of white fat due to abnormally activated BMP signaling.
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