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- Title
A Novel Bone Morphogenetic Protein 2 Mutant Mouse, nBmp2NLS<sup>tm</sup>, Displays Impaired Intracellular Ca<sup>2+</sup> Handling in Skeletal Muscle.
- Authors
Bridgewater, Laura C.; Mayo, Jaime L.; Evanson, Bradley G.; Whitt, Megan E.; Dean, Spencer A.; Yates, Joshua D.; Holden, Devin N.; Schmidt, Alina D.; Fox, Christopher L.; Dhunghel, Saroj; Steed, Kevin S.; Adam, Michael M.; Nichols, Caitlin A.; Loganathan, Sampath K.; Barrow, Jeffery R.; Hancock, Chad R.
- Abstract
We recently reported a novel form of BMP2, designated nBMP2, which is translated from an alternative downstream start codon and is localized to the nucleus rather than secreted from the cell. To examine the function of nBMP2 in the nucleus, we engineered a gene-targeted mutant mouse model (nBmp2NLStm) in which nBMP2 cannot be translocated to the nucleus. Immunohistochemistry demonstrated the presence of nBMP2 staining in the myonuclei of wild type but not mutant skeletal muscle. The nBmp2NLStm mouse exhibits altered function of skeletal muscle as demonstrated by a significant increase in the time required for relaxation following a stimulated twitch contraction. Force frequency analysis showed elevated force production in mutant muscles compared to controls from 10 to 60 Hz stimulation frequency, consistent with the mutant muscle's reduced ability to relax between rapidly stimulated contractions. Muscle relaxation after contraction is mediated by the active transport of Ca2+ from the cytoplasm to the sarcoplasmic reticulum by sarco/endoplasmic reticulum Ca2+ ATPase (SERCA), and enzyme activity assays revealed that SERCA activity in skeletal muscle from nBmp2NLStm mice was reduced to approximately 80% of wild type. These results suggest that nBMP2 plays a role in the establishment or maintenance of intracellular Ca2+ transport pathways in skeletal muscle.
- Publication
BioMed Research International, 2013, Vol 2013, p1
- ISSN
2314-6133
- Publication type
Article
- DOI
10.1155/2013/125492