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1.
Geroscience ; 46(1): 1285-1302, 2024 Feb.
Article in English | MEDLINE | ID: mdl-37535205

ABSTRACT

Onset and rates of sarcopenia, a disease characterized by a loss of muscle mass and function with age, vary greatly between sexes. Currently, no clinical interventions successfully arrest age-related muscle impairments since the decline is frequently multifactorial. Previously, we found that systemic transplantation of our unique adult multipotent muscle-derived stem/progenitor cells (MDSPCs) isolated from young mice-but not old-extends the health-span in DNA damage mouse models of progeria, a disease of accelerated aging. Additionally, induced neovascularization in the muscles and brain-where no transplanted cells were detected-strongly suggests a systemic therapeutic mechanism, possibly activated through circulating secreted factors. Herein, we used ZMPSTE24-deficient mice, a lamin A defect progeria model, to investigate the ability of young MDSPCs to preserve neuromuscular tissue structure and function. We show that progeroid ZMPST24-deficient mice faithfully exhibit sarcopenia and age-related metabolic dysfunction. However, systemic transplantation of young MDSPCs into ZMPSTE24-deficient progeroid mice sustained healthy function and histopathology of muscular tissues throughout their 6-month life span in a sex-specific manner. Indeed, female-but not male-mice systemically transplanted with young MDSPCs demonstrated significant preservation of muscle endurance, muscle fiber size, mitochondrial respirometry, and neuromuscular junction morphometrics. These novel findings strongly suggest that young MDSPCs modulate the systemic environment of aged animals by secreted rejuvenating factors to maintain a healthy homeostasis in a sex-specific manner and that the female muscle microenvironment remains responsive to exogenous regenerative cues in older age. This work highlights the age- and sex-related differences in neuromuscular tissue degeneration and the future prospect of preserving health in older adults with systemic regenerative treatments.


Subject(s)
Adult Stem Cells , Progeria , Sarcopenia , Male , Mice , Female , Animals , Progeria/genetics , Disease Models, Animal , Adult Stem Cells/metabolism , Muscles/metabolism
2.
Muscle Nerve ; 61(5): 616-622, 2020 05.
Article in English | MEDLINE | ID: mdl-32086830

ABSTRACT

INTRODUCTION: Evaluation of nerve mechanical properties has the potential to improve assessment of nerve impairment. Shear wave velocity, as measured by using shear wave (SW) ultrasound elastography, is a promising indicator of nerve mechanical properties such as stiffness. However, elucidation of external factors that influence SW velocity, particularly nerve tension, is required for accurate interpretations. METHODS: Median and ulnar nerve SW velocities were measured at proximal and distal locations with limb positions that indirectly altered nerve tension. RESULTS: Shear wave velocity was greater at proximal and distal locations for limb positions that induced greater tension in the median (mean increase proximal 89.3%, distal 64%) and ulnar (mean increase proximal 91.1%, distal 37.4%) nerves. DISCUSSION: Due to the influence of nerve tension when SW ultrasound elastography is used, careful consideration must be given to limb positioning.


Subject(s)
Elasticity Imaging Techniques/methods , Median Nerve/diagnostic imaging , Posture , Ulnar Nerve/diagnostic imaging , Upper Extremity , Adolescent , Adult , Biomechanical Phenomena , Female , Healthy Volunteers , Humans , Male , Median Nerve/anatomy & histology , Median Nerve/physiology , Organ Size , Ulnar Nerve/anatomy & histology , Ulnar Nerve/physiology , Ultrasonography/methods , Young Adult
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