Abstract
Extraocular muscles (EOM) have a strikingly different disease profile than limb skeletal muscles. It has long been known that they are spared in Duchenne (DMD) and other forms of muscular dystrophy. Despite many studies, the cause for this sparing is not understood. We have proposed that differences in myogenic precursor cell properties in EOM maintain normal morphology over the lifetime of individuals with DMD due to either greater proliferative potential or greater resistance to injury. This hypothesis was tested by exposing wild type and mdx:utrophin+/− (het) mouse EOM and limb skeletal muscles to 18 Gy gamma irradiation, a dose known to inhibit satellite cell proliferation in limb muscles. As expected, over time het limb skeletal muscles displayed reduced central nucleation mirrored by a reduction in Pax7-positive cells, demonstrating a significant loss in regenerative potential. In contrast, in the first month post-irradiation in the het EOM, myofiber cross-sectional areas first decreased, then increased, but ultimately returned to normal compared to non-irradiated het EOM. Central nucleation significantly increased in the first post-irradiation month, resembling the dystrophic limb phenotype. This correlated with decreased EECD34 stem cells and a concomitant increase and subsequent return to normalcy of both Pax7 and Pitx2-positive cell density. By two months, normal het EOM morphology returned. It appears that irradiation disrupts the normal method of EOM remodeling, which react paradoxically to produce increased numbers of myogenic precursor cells. This suggests that the EOM contain myogenic precursor cell types resistant to 18 Gy gamma irradiation, allowing return to normal morphology 2 months post-irradiation. This supports our hypothesis that ongoing proliferation of specialized regenerative populations in the het EOM actively maintains normal EOM morphology in DMD. Ongoing studies are working to define the differences in the myogenic precursor cells in EOM as well as the cellular milieu in which they reside.
Highlights
Skeletal muscle has a remarkable capacity for regeneration after injury and in disease
Not all skeletal muscles are affected by Duchenne muscular dystrophy (DMD), and notable exceptions exist that appear to be completely spared in DMD and related muscular dystrophies
One candidate population enriched in the extraocular muscles (EOM) compared to limb skeletal muscle that we previously identified is the EECD34 cell population, which is CD34+/Sca12/CD312/CD452 [23], [24]
Summary
Skeletal muscle has a remarkable capacity for regeneration after injury and in disease. The process of regeneration is dependent on a population of myogenic precursor cells that were originally defined by their position between the sarcolemma and basal lamina and called satellite cells [1]. Upon injury, these myogenic precursor cells are activated and begin a process of proliferation and self-renewal. In diseases like Duchenne muscular dystrophy (DMD) and in age-related sarcopenia, the regenerative capacity of limb and body skeletal muscle becomes exhausted primarily due to exhaustion of the satellite cell pool after repeated cycles of muscle degeneration and regeneration, leading to a loss of muscle mass and function [5], [6], [7], [8], [9]. Spared skeletal muscles include a number of craniofacial muscles, including the laryngeal and extraocular muscles [10], [11]
Sign-in/Register to view highlights & summary Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
