Satellite cells isolated from aged or dystrophic muscle exhibit a reduced capacity to promote angiogenesis in vitro

Biochemical and Biophysical Research Communications

Volumn 440, Issue 3, 2013, Pages 399-404

  Rhoads, R P ^a,b   Flann, K L ^a   Cardinal, T R ^a   Rathbone, C R ^a   Liu, X ^a   Allen, R E ^a  

^a UNIVERSITY OF ARIZONA   (United States)

^b VIRGINIA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY   (United States)

Author keywords

Aging; Angiogenesis; Muscular dystrophy; Satellite cell; Skeletal muscle

Indexed keywords

HYPOXIA INDUCIBLE FACTOR 1ALPHA; MESSENGER RNA; VASCULOTROPIN;

ADIPOSE TISSUE; ANGIOGENESIS; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL ISOLATION; CELL PROLIFERATION; CONTROLLED STUDY; DUCHENNE MUSCULAR DYSTROPHY; GENE EXPRESSION; IN VITRO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN SECRETION; RAT; SATELLITE CELL; SKELETAL MUSCLE; WILD TYPE;

MUS; RATTUS;

AGING; ANGIOGENESIS; MUSCULAR DYSTROPHY; SATELLITE CELL; SKELETAL MUSCLE;

AGING; ANIMALS; CELL SEPARATION; CELLS, CULTURED; COCULTURE TECHNIQUES; GENE EXPRESSION REGULATION; HYPOXIA-INDUCIBLE FACTOR 1, ALPHA SUBUNIT; MICE; MICE, INBRED MDX; MUSCULAR DYSTROPHIES; NEOVASCULARIZATION, PHYSIOLOGIC; RATS; RATS, SPRAGUE-DAWLEY; SATELLITE CELLS, SKELETAL MUSCLE; VASCULAR ENDOTHELIAL GROWTH FACTOR A;

EID: 84888130476     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2013.09.085     Document Type: Article

References (33)

1. Chargé S.B., Rudnicki M.A. Cellular and molecular regulation of muscle regeneration. Physiol. Rev. 2004, 84:209-238.
2. Relaix F., Zammit P.S. Satellite cells are essential for skeletal muscle regeneration: the cell on the edge returns centre stage. Development 2012, 139:2845-2856.
3. Christov C., Chretien F., Abou-Khalil R., Bassez G., Vallet G., Authier F.J., Bassaglia Y., Shinin V., Tajbakhsh S., Chazaud B., Gherardi R.K. Muscle satellite cells and endothelial cells: close neighbors and privileged partners. Mol. Biol. Cell 2007, 18:1397-1409.
4. Rhoads R.P., Johnson R.M., Rathbone C.R., Liu X., Temm-Grove C., Sheehan S.M., Hoying J.B., Allen R.E. Satellite cell mediated angiogenesis coincides with a functional hypoxia-inducible factor (HIF) pathway. Am. J. Physiol. Cell Physiol. 2009, 296:C1321-8.
5. Markley J.M., Faulkner J.A., Carlson B.M. Regeneration of skeletal muscle after grafting in monkeys. Plast. Reconstr. Surg. 1978, 62:415-422.
6. Hansen-Smith F.M., Carlson B.M. Cellular responses to free grafting of the extensor digitorum longus muscle of the rat. J. Neurol. Sci. 1979, 41:149-173.
7. Hansen-Smith F.M., Carlson B.M., Irwin K.L. Revascularization of the freely grafted extensor digitorum longus muscle in the rat. Am. J. Anat. 1980, 158:65-82.
8. Jang Y.C., Sinha M., Cerletti M., Dall'Osso C., Wagers A.J. Skeletal muscle stem cells: effects of aging and metabolism on muscle regenerative function. Cold Spring Harb. Symp. Quant. Biol. 2011, 76:101-111.
9. Rüegg M.A., Glass D.J. Molecular mechanisms and treatment options for muscle wasting diseases. Annu. Rev. Pharmacol. Toxicol. 2011, 51:373-395.
10. Webster C., Blau H.M. Accelerated age-related decline in replicative life-span of Duchenne muscular dystrophy myoblasts: implications for cell and gene therapy. Somat. Cell Mol. Genet. 1990, 16:557-565.
11. Snow M.H. The effects of aging on satellite cells in skeletal muscles of mice and rats. Cell Tissue Res. 1977, 185:399-408.
12. Schultz E., Lipton B.H. Skeletal muscle satellite cells: changes in proliferation potential as a function of age. Mech. Ageing Dev. 1982, 20:377-383.
13. Schultz E., Jaryszak D.L. Effects of skeletal muscle regeneration on the proliferation potential of satellite cells. Mech. Ageing Dev. 1985, 30:63-72.
14. Brack A.S., Rando T.A. Intrinsic changes and extrinsic influences of myogenic stem cell function during aging. Stem Cell Rev. 2007, 3:226-237.
15. Lee A.S., Anderson J.E., Joya J.E., Head S.I., Pather N., Kee A.J., Gunning P.W., Hardeman E.C. Aged skeletal muscle retains the ability to fully regenerate functional architecture. Bioarchitecture 2013, 3:25-37.
16. Decary S., Mouly V., Hamida C.B., Sautet A., Barbet J.P., Butler-Browne G.S. Replicative potential and telomere length in human muscle: implications for satellite cell mediated gene therapy. Hum. Gene Ther. 1997, 8:1429-1438.
17. Nguyen F., Guigand L., Goubault-Leroux I., Wyers M., Cherel Y. Microvessel density in muscles of dogs with golden retriever muscular dystrophy. Neuromuscul. Disord. 2005, 15:154-163.
18. Ryan N.A., Zwetsloot K.A., Westerkamp L.M., Hickner R.C., Pofahl W.E., Gavin T.P. Lower skeletal muscle capillarization and VEGF expression in aged vs. young men. J. Appl. Physiol. 2006, 100:178-185.
19. Allen R.E., Temm-Grove C.J., Sheehan S.M., Rice G. Skeletal muscle satellite cell cultures. Methods Cell Biol. 1998, 52:155-176.
20. Rathbone C.R., Yamanouchi K., Chen X.K., Nevoret-Bell C.J., Rhoads R.P., Allen R.E. Effects of transforming growth factor-beta (TGF-β1) on satellite cell activation and survival during oxidative stress. J. Muscle Res. Cell Motil. 2011, 32:99-109.
21. Hoying J.B., Boswell C.A., Williams S.K. Angiogenic potential of microvessel fragments established in three-dimensional collagen gels. In Vitro Cell. Dev. Biol. Anim. 1996, 32:409-419.
22. Vartanian K.B., Chen H.Y.S., Kennedy J., Beck S.K., Ryaby J.T., Wang H., Hoying J.B. The non-proteolytically active thrombin peptide TP508 stimulates angiogenic sprouting. J. Cell. Physiol. 2006, 206:175-180.
23. Schmalbruch H., Hellhammer U. The number of satellite cells in normal human muscle. Anat. Rec. 1976, 185:279-287.
24. Hoffman E.P., Brown R.H., Kunkel L.M. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 1987, 51:919-928.
25. Sicinski P., Geng Y., Ryder-Cook A.S., Barnard E.A., Darlison M.G., Barnard P.J. The molecular basis of muscular dystrophy in the mdx mouse: a point mutation. Science 1989, 244:1578-1580.
26. Pastoret C., Sebille A. Age-related differences in regeneration of dystrophic (mdx) and normal muscle in the mouse. Muscle Nerve 1995, 18:1147-1154.
27. Pastoret C., Sebille A. Mdx mice show progressive weakness and muscle deterioration with age. J. Neurosci. 1995, 129:97-105.
28. Lefaucheur J.P., Pastoret C., Sebille A. Phenotype of dystrophinopathy in old mdx mice. Anat. Rec. 1995, 242:70-76.
29. Blau H.M., Webster C., Pavlath G.K. Defective myoblasts identified in Duchenne muscular dystrophy. Proc. Natl. Acad. Sci. USA 1983, 80:4856-4860.
30. Heslop L., Morgan J.E., Partridge T.A. Evidence for a myogenic stem cell that is exhausted in dystrophic muscle. J. Cell Sci. 2000, 113:2299-2308.
31. Messina S., Mazzeo A., Bitto A., Aguennouz M., Migliorato A., De Pasquale M.G., Minutoli L., Altavilla D., Zentilin L., Giacca M., Squadrito F., Vita G. VEGF overexpression via adeno-associated virus gene transfer promotes skeletal muscle regeneration and enhances muscle function in mdx mice. FASEB J. 2007, 21:3737-3746.
32. Deasy B.M., Feduska J.M., Payne T.R., Li Y., Ambrosio F., Huard J. Effect of VEGF on the regenerative capacity of muscle stem cells in dystrophic skeletal muscle. Mol. Ther. 2009, 17:1788-1798.
33. Wagatsuma A. Effect of aging on expression of angiogenesis-related factors in mouse skeletal muscle. Exp. Gerontol. 2006, 41:49-54.