Key result
Simultaneous assessment of isometric force and second harmonic generation imaging in single muscle fibers demonstrated significant correlations between myofibrillar ultrastructure and biomechanical performance, allowing optical prediction of force output.
A novel combined biomechatronics and imaging system enables the noninvasive prediction of single muscle fiber force output from multiphoton images, with potential applications in diagnosing myopathies.
May enable noninvasive muscle remodeling assessment; leaves open validation for functional prediction in disease.
Skeletal muscle is an archetypal organ whose structure is tuned to match function. The magnitude of order in muscle fibers and myofibrils containing motor protein polymers determines the directed force output of the summed force vectors and, therefore, the muscle’s power performance on the structural level. Structure and function can change dramatically during disease states involving chronic remodeling. Cellular remodeling of the cytoarchitecture has been pursued using noninvasive and label-free multiphoton second harmonic generation (SHG) microscopy. Hereby, structure parameters can be extracted as a measure of myofibrillar order and thus are suggestive of the force output that a remodeled structure can still achieve. However, to date, the parameters have only been an indirect measure, and a precise calibration of optical SHG assessment for an exerted force has been elusive as no technology in existence correlates these factors. We engineered a novel, automated, high-precision biomechatronics system into a multiphoton microscope allows simultaneous isometric Ca 2+ -graded force or passive viscoelasticity measurements and SHG recordings. Using this MechaMorph system, we studied force and SHG in single EDL muscle fibers from wt and mdx mice; the latter serves as a model for compromised force and abnormal myofibrillar structure. We present Ca 2+ -graded isometric force, pCa-force curves, passive viscoelastic parameters and 3D structure in the same fiber for the first time. Furthermore, we provide a direct calibration of isometric force to morphology, which allows noninvasive prediction of the force output of single fibers from only multiphoton images, suggesting a potential application in the diagnosis of myopathies.
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Schneidereit et al. (2018) studied Muscular Dystrophy (mdx mouse model). MechaMorph system (combined biomechatronics and SHG imaging) vs. Wild-type mice was evaluated on Correlation between SHG-derived structural parameters (CAS, VD) and active isometric force/passive viscoelasticity. Simultaneous assessment of isometric force and second harmonic generation imaging in single muscle fibers demonstrated significant correlations between myofibrillar ultrastructure and biomechanical performance, allowing optical prediction of force output.
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