Skeletal muscle tissue is repaired and maintained for the lifetime of mammalian organisms with the exception of functional muscle loss and atrophy in the aged. The adult stem cell thought to be responsible for re- generating and maintaining skeletal muscle tissue is the satellite cell, so named for its anatomical localization in skeletal muscle tissue sandwiched between the plasma membrane of the myofiber and the extracellular matrix. This unique niche imposes asymmetry on the satellite cell, allowing signaling from the external environment as well as from the underlying myofiber. The mechanisms involved in the renewal of the satellite cell are not well understood as a number of groups have identified subsets of satellite cells that exhibit enhanced engraftment into skeletal muscle tissue. A number of groups, including ours have shown that engrafted satellite cells are capable of self-renewal during skeletal muscle repair. A number of important questions regarding satellite cell self-renewal have not been addressed. When do satellite cells self-renew? How are satellite cell numbers maintained? What mechanisms are responsible for satellite cell self-renewal? Are all satellite cells equivalent? These basic questions regarding satellite cell self-renewal remain unanswered. Additional analysis has revealed that satellite-SP cells express JamB, a junctional adhesion protein involved in cell polarity, which binds the Par complex is present in satellite-SP cells. Second, Jam-B cells express Par-3, which is asymmetric and co-localizes with asymmetric Syndecan-4. When prospectively isolated, Syndecan-4+/Jam-B+ cultures maintain Pax7 expressing """"""""reserve"""""""" cells while Pax7 is not detectable in Syndecan-4+Jam-B- satellite cell ex- plants, which all terminally differentiate. Our recently submitted manuscript provides evidence for a signaling pathway whereby asymmetric localization of Par complex in turn asymmetrically activates p38????MAPK inducing MyoD in one daughter cell during the first satellite cell division following explant. The other daughter fails to induce MyoD and re-acquires a quiescent """"""""reserve"""""""" phenotype. We propose that Syndecan-4 and Jam- B signaling coordinated by extracellular signals commits a satellite cell to asymmetric division. A primary goal of our experimental plan is to test this hypothesis and provide evidence for a Syndecan-47Jam-B complex that is required for asymmetric division of satellite cells.

Public Health Relevance

Skeletal muscle is essential for respiration, locomotion, and elimination of waste. Severe loss of skeletal muscle is catastrophic, shortening lifespan, dramatically reducing overall quality of life and incurring significant health care costs. Severe loss of muscle function occurs during normal aging and in neuromuscular diseases. The loss of skeletal muscle function is likely due to loss of regenerative capacity and the ability of adult muscle stem cells to renew themselves. We propose research to better understand how adult muscle stem cells are regulated aiding in the development of stem cell therapies.

National Institute of Health (NIH)
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Research Project (R01)
Project #
Application #
Study Section
Skeletal Muscle and Exercise Physiology Study Section (SMEP)
Program Officer
Boyce, Amanda T
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
University of Colorado at Boulder
Schools of Arts and Sciences
United States
Zip Code
Pawlikowski, Bradley; Vogler, Thomas Orion; Gadek, Katherine et al. (2017) Regulation of skeletal muscle stem cells by fibroblast growth factors. Dev Dyn 246:359-367
Hall, Monica N; Hall, John K; Cadwallader, Adam B et al. (2017) Transplantation of Skeletal Muscle Stem Cells. Methods Mol Biol 1556:237-244
Harper, Shavonn C; Brack, Andrew; MacDonnell, Scott et al. (2016) Is Growth Differentiation Factor 11 a Realistic Therapeutic for Aging-Dependent Muscle Defects? Circ Res 118:1143-50; discussion 1150
Pisconti, Addolorata; Banks, Glen B; Babaeijandaghi, Farshad et al. (2016) Loss of niche-satellite cell interactions in syndecan-3 null mice alters muscle progenitor cell homeostasis improving muscle regeneration. Skelet Muscle 6:34
Chenette, Devon M; Cadwallader, Adam B; Antwine, Tiffany L et al. (2016) Targeted mRNA Decay by RNA Binding Protein AUF1 Regulates Adult Muscle Stem Cell Fate, Promoting Skeletal Muscle Integrity. Cell Rep 16:1379-1390
Pawlikowski, Bradley; Pulliam, Crystal; Betta, Nicole Dalla et al. (2015) Pervasive satellite cell contribution to uninjured adult muscle fibers. Skelet Muscle 5:42
Bustos, Francisco; de la Vega, Eduardo; Cabezas, Felipe et al. (2015) NEDD4 Regulates PAX7 Levels Promoting Activation of the Differentiation Program in Skeletal Muscle Precursors. Stem Cells 33:3138-51
Doles, Jason D; Olwin, Bradley B (2015) Muscle stem cells on the edge. Curr Opin Genet Dev 34:24-8
Hausburg, Melissa A; Doles, Jason D; Clement, Sandra L et al. (2015) Post-transcriptional regulation of satellite cell quiescence by TTP-mediated mRNA decay. Elife 4:e03390
Bernet, Jennifer D; Doles, Jason D; Hall, John K et al. (2014) p38 MAPK signaling underlies a cell-autonomous loss of stem cell self-renewal in skeletal muscle of aged mice. Nat Med 20:265-71

Showing the most recent 10 out of 20 publications