Promoting and accelerating muscle regeneration through cell therapy in a mouse model.

J Taibah Univ Med Sci

Experimental Therapy Department, Iraqi Center for Cancer and Medical Genetic Research, Mustansiriyah University, Baghdad, Iraq.

Published: October 2024

AI Article Synopsis

  • Skeletal muscle injuries are common and can lead to chronic pain and disability, making the search for effective treatments critical.
  • This study explores the potential of mesenchymal stem cells (MSCs) from mouse bone marrow to regenerate damaged skeletal muscle by differentiating them into muscle cells.
  • Results show that differentiated muscle cells (myocytes) from MSCs significantly enhance muscle repair compared to undifferentiated stem cells, suggesting a promising biological approach for treating muscle atrophy and related disorders.

Article Abstract

Objectives: Skeletal muscle injuries and disorders are universal clinical challenges with direct and indirect mechanisms and notable residual effects, such as prolonged, intense pain and physical disability. Stem cells, an innovative tool for cell therapy for musculoskeletal disorders, specifically promote skeletal muscle regeneration. This study was aimed at investigating the use of mesenchymal stem cells (MSCs) and their differentiated myocytes as a cell-based therapy to promote regeneration in damaged or diseased skeletal muscle.

Methods: Bone marrow mesenchymal stem cells (BM-MSCs) were isolated from the bone marrow of adult mice and grown in tissue culture flasks. The BM-MSCs were positive for CD90 and CD105, and negative for CD45 and CD34. These cells were induced with specific differentiation medium to differentiate into a skeletal muscle cell lineage over 7 days. Skeletal muscle differentiation was characterized according to morphology through hematoxylin and eosin staining, and scanning electron microscopy. Immunostaining for Myf-6, myosin heavy chain (MHC), and desmin-specific factors for skeletal muscle development-was performed to confirm skeletal muscle differentiation. An study in a muscle injury model was used to evaluate cell therapy based on naïve stem cells and differentiated myocytes.

Results: Cultured mouse BM-MSCS were positive for CD90 and CD105, and negative for CD45 and CD34. These cells developed into skeletal muscle with strong skeletal muscle differentiation potential, as confirmed by immunohistochemistry for the markers Myf6, MHC, and desmin. The differentiated myocytes showed better repair enhancement than undifferentiated stem cells after transplantations into a mouse model of skeletal muscle atrophy.

Conclusions: Myocytes derived from BM-MSCs may be incorporated into muscular atrophy treatment as a biological strategy for managing skeletal muscle diseases and injuries, thus advancing cell-based clinical treatments.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11526084PMC
http://dx.doi.org/10.1016/j.jtumed.2024.09.004DOI Listing

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