Muscle stem cells on the edge

Current Opinion in Genetics and Development

Volumn 34, Issue , 2015, Pages 24-28

  Doles, Jason D ^a   Olwin, Bradley B ^a  

^a UNIVERSITY OF COLORADO   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MESSENGER RNA; MITOGEN ACTIVATED PROTEIN KINASE P38; RNA;

AGING; CELL ACTIVATION; CELL FUNCTION; CELL METABOLISM; HUMAN; INTRACELLULAR SIGNALING; MUSCLE DISEASE; MUSCLE STEM CELL; OXIDATIVE STRESS; PATHOPHYSIOLOGY; PRIORITY JOURNAL; REVIEW; RNA ANALYSIS; RNA STABILITY; TRANSCRIPTION REGULATION; CELL AGING; CELL DIFFERENTIATION; CELL PROLIFERATION; CYTOLOGY; GENETICS; GROWTH, DEVELOPMENT AND AGING; HOMEOSTASIS; METABOLISM; SIGNAL TRANSDUCTION; SKELETAL MUSCLE; STEM CELL;

CELL AGING; CELL DIFFERENTIATION; CELL PROLIFERATION; HOMEOSTASIS; HUMANS; MUSCLE, SKELETAL; RNA STABILITY; RNA, MESSENGER; SIGNAL TRANSDUCTION; STEM CELLS;

EID: 84937145197     PISSN: 0959437X     EISSN: 18790380     Source Type: Journal    
DOI: 10.1016/j.gde.2015.06.006     Document Type: Review

References (32)

1. Kuang S., Kuroda K., Le Grand F., Rudnicki M.A. Asymmetric self-renewal and commitment of satellite stem cells in muscle. Cell 2007, 129:999-1010.
2. Rudnicki M.A., Schnegelsberg P.N., Stead R.H., Braun T., Arnold H.H., Jaenisch R. MyoD or Myf-5 is required for the formation of skeletal muscle. Cell 1993, 75:1351-1359.
3. Cornelison D.D., Olwin B.B., Rudnicki M.A., Wold B.J. MyoD(-/-) satellite cells in single-fiber culture are differentiation defective and MRF4 deficient. Dev Biol 2000, 224:122-137.
4. Jones N.C., Tyner K.J., Nibarger L., Stanley H.M., Cornelison D.D.W., Fedorov Y.V., Olwin B.B. The p38{alpha}/{beta} MAPK functions as a molecular switch to activate the quiescent satellite cell. J Cell Biol 2005, 169:105-116.
5. Crist C.G., Montarras D., Buckingham M. Muscle satellite cells are primed for myogenesis but maintain quiescence with sequestration of Myf5 mRNA targeted by microRNA-31 in mRNP granules. Cell Stem Cell 2012, 11:118-126.
6. Farina N.H., Hausburg M., Dalla Betta N., Pulliam C., Srivastava D., Cornelison D.D., Olwin B.B. A role for RNA post-transcriptional regulation in satellite cell activation. Skelet Muscle 2012, 2:21.
7. Cornelison D.D.W., Wold B.J. Single-cell analysis of regulatory gene expression in quiescent and activated mouse skeletal muscle satellite cells. Dev Biol 1997, 191:270-283.
8. Jones N.C., Fedorov Y.V., Rosenthal R.S., Olwin B.B. ERK1/2 is required for myoblast proliferation but is dispensable for muscle gene expression and cell fusion. J Cell Physiol 2001, 186:104-115.
9. Troy A., Cadwallader A.B., Fedorov Y., Tyner K., Tanaka K.K., Olwin B.B. Coordination of satellite cell activation and self-renewal by par-complex-dependent asymmetric activation of p38α/β MAPK. Cell Stem Cell 2012, 11:541-553.
10. Bernet J.D., Doles J.D., Hall J.K., Kelly Tanaka K., Carter T.A., Olwin B.B. p38 MAPK signaling underlies a cell-autonomous loss of stem cell self-renewal in skeletal muscle of aged mice. Nat Med 2014, 20:265-271.
11. Cosgrove B.D., Gilbert P.M., Porpiglia E., Mourkioti F., Lee S.P., Corbel S.Y., Llewellyn M.E., Delp S.L., Blau H.M. Rejuvenation of the muscle stem cell population restores strength to injured aged muscles. Nat Med 2014, 20:255-264.
12. Siegel A.L., Atchison K., Fisher K.E., Davis G.E., Cornelison D.D.W. 3D timelapse analysis of muscle satellite cell motility. Stem Cells 2009, 27:2527-2538.
13. Chen C., Liu Y., Liu R., Ikenoue T., Guan K.-L., Liu Y., Zheng P. TSC-mTOR maintains quiescence and function of hematopoietic stem cells by repressing mitochondrial biogenesis and reactive oxygen species. J Exp Med 2008, 205:2397-2408.
14. Rodgers J.T., King K.Y., Brett J.O., Cromie M.J., Charville G.W., Maguire K.K., Brunson C., Mastey N., Liu L., et al. mTORC1 controls the adaptive transition of quiescent stem cells from G0 to G(Alert). Nature 2014, 510:393-396.
15. Hausburg M.A., Doles J.D., Clement S.L., Cadwallader A.B., Hall M.N., Blackshear P.J., Lykke-Andersen J., Olwin B.B. Post-transcriptional regulation of satellite cell quiescence by TTP-mediated mRNA decay. Elife 2015, 4:e03390.
16. Cheung T.H., Quach N.L., Charville G.W., Liu L., Park L., Edalati A., Yoo B., Hoang P., Rando T.A. Maintenance of muscle stem-cell quiescence by microRNA-489. Nature 2012, 482:524-528.
17. Jash S., Dhar G., Ghosh U., Adhya S. Role of the mTORC1 complex in satellite cell activation by RNA-induced mitochondrial restoration: dual control of cyclin D1 through microRNAs. Mol Cell Biol 2014, 34:3594-3606.
18. Brengues M., Teixeira D., Parker R. Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies. Science 2005, 310:486-489.
19. Bhattacharyya S.N., Habermacher R., Martine U., Closs E.I., Filipowicz W. Relief of microRNA-mediated translational repression in human cells subjected to stress. Cell 2006, 125:1111-1124.
20. Lai W.S., Parker J.S., Grissom S.F., Stumpo D.J., Blackshear P.J. Novel mRNA targets for tristetraprolin (TTP) identified by global analysis of stabilized transcripts in TTP-deficient fibroblasts. Mol Cell Biol 2006, 26:9196-9208.
21. Fardaei M., Rogers M.T., Thorpe H.M., Larkin K., Hamshere M.G., Harper P.S., Brook J.D. Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells. Hum Mol Genet 2002, 11:805-814.
22. Klar J., Sobol M., Melberg A., Mäbert K., Ameur A., Johansson A.C.V., Feuk L., Entesarian M., Orlén H., et al. Welander distal myopathy caused by an ancient founder mutation in TIA1 associated with perturbed splicing. Hum Mutat 2013, 34:572-577.
23. Corbeil-Girard L.-P., Klein A.F., Sasseville A.M.-J., Lavoie H., Dicaire M.-J., Saint-Denis A., Pagé M., Duranceau A., Codère F., et al. PABPN1 overexpression leads to upregulation of genes encoding nuclear proteins that are sequestered in oculopharyngeal muscular dystrophy nuclear inclusions. Neurobiol Dis 2005, 18:551-567.
24. Olivé M., Janué A., Moreno D., Gámez J., Torrejón-Escribano B., Ferrer I. TAR DNA-binding protein 43 accumulation in protein aggregate myopathies. J Neuropathol Exp Neurol 2009, 68:262-273.
25. Malatesta M., Perdoni F., Muller S., Zancanaro C., Pellicciari C. Nuclei of aged myofibres undergo structural and functional changes suggesting impairment in RNA processing. Eur J Histochem 2009, 53:97-106.
26. Malatesta M., Giagnacovo M., Costanzo M., Cisterna B., Cardani R., Meola G. Muscleblind-like1 undergoes ectopic relocation in the nuclei of skeletal muscles in myotonic dystrophy and sarcopenia. Eur J Histochem 2013, 57:e15.
27. Deleault K.M., Skinner S.J., Brooks S.A. Tristetraprolin regulates TNF TNF-alpha mRNA stability via a proteasome dependent mechanism involving the combined action of the ERK and p38 pathways. Mol Immunol 2008, 45:13-24.
28. Skriner K., Hueber W., Süleymanoglu E., Höfler E., Krenn V., Smolen J., Steiner G. AUF1, the regulator of tumor necrosis factor alpha messenger RNA decay, is targeted by autoantibodies of patients with systemic rheumatic diseases. Arthritis Rheum 2008, 58:511-520.
29. Zhang L., Lee J.E., Wilusz J., Wilusz C.J. The RNA-binding protein CUGBP1 regulates stability of tumor necrosis factor mRNA in muscle cells: implications for myotonic dystrophy. J Biol Chem 2008, 283:22457-22463.
30. Piecyk M., Wax S., Beck A.R., Kedersha N., Gupta M., Maritim B., Chen S., Gueydan C., Kruys V., et al. TIA-1 is a translational silencer that selectively regulates the expression of TNF-alpha. EMBO J 2000, 19:4154-4163.
31. Tahir T.A., Singh H., Brindle N.P.J. The RNA binding protein hnRNP-K mediates post-transcriptional regulation of uncoupling protein-2 by angiopoietin-1. Cell Signal 2014, 26:1379-1384.
32. Briata P., Forcales S.V., Ponassi M., Corte G., Chen C.-Y., Karin M., Puri P.L., Gherzi R. p38-dependent phosphorylation of the mRNA decay-promoting factor KSRP controls the stability of select myogenic transcripts. Mol Cell 2005, 20:891-903.