Bone marrow-derived stem cell interactions with adult cardiomyocytes and skeletal myoblasts in vitro

Cardiovascular Revascularization Medicine

Volumn 7, Issue 4, 2006, Pages 222-230

  Baffour, Richard ^a   Pakala, Rajbabu ^a   Hellinga, David ^a   Joner, Michael ^b   Okubagzi, Petros ^a   Epstein, Stephen E ^a   Waksman, Ron ^a  

^a WASHINGTON HOSPITAL CENTER   (United States)

^b CVPATH INSTITUTE   (United States)

Author keywords

Cardiomyocytes; Myoblasts; Stem cells

Indexed keywords

MONOCYTE CHEMOTACTIC PROTEIN 1; SCATTER FACTOR; VASCULOTROPIN;

ARTICLE; BONE MARROW DERIVED MONONUCLEAR CELL CONDITIONED MEDIUM; BONE MARROW DERIVED STEM CELL; BONE MARROW STROMAL CELL CONDITIONED MEDIUM; CELL CONTACT; CELL CULTURE; CELL FUNCTION; CELL INTERACTION; CELL PROLIFERATION; COCULTURE; CONTROLLED STUDY; CULTURE MEDIUM; ENZYME LINKED IMMUNOSORBENT ASSAY; HEART MUSCLE CELL; HEMATOPOIETIC STEM CELL; HUMAN; HUMAN CELL; MYOBLAST; PRIORITY JOURNAL; STROMA CELL;

ANALYSIS OF VARIANCE; BONE MARROW CELLS; CELLS, CULTURED; CHEMOKINE CCL2; ENZYME-LINKED IMMUNOSORBENT ASSAY; HEPATOCYTE GROWTH FACTOR; HUMANS; INSULIN-LIKE GROWTH FACTOR BINDING PROTEIN 1; MYOBLASTS, SKELETAL; MYOCYTES, CARDIAC; STEM CELLS; VASCULAR ENDOTHELIAL GROWTH FACTOR A;

EID: 33845463899     PISSN: 15538389     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.carrev.2006.06.005     Document Type: Article

References (29)

1. Orlic D., Kajstura J., Chimenti S., Jakoniuk I., Anderson S., Li B., Pickel J., McKay R., Nadal-Ginard B., Bodine D., Leri A., and Anversa P. Bone marrow cells regenerate infarcted myocardium. Nature 410 (2001) 701-705
2. Kocher A., Schuster M., Szabolcs M., Takuma S., Burkhoff D., Wang J., Homma S., Edwards N., and Itescu S. Neovascularization of ischemic myocardium by human bone-marrow-derived angioblasts prevents cardiomyocyte apoptosis, reduces remodeling and improves cardiac function. Nat Med 7 (2001) 430-436
3. Fuchs S., Baffour R., Zhou Y., Shou M., Pierre A., Tio F., Weissman N., Leon M., Epstein S., and Kornowski R. Transendocardial delivery of autologous bone marrow enhances collateral perfusion and regional function in pigs with chronic experimental myocardial ischemia. J Am Coll Cardiol 37 (2001) 1726-1732
4. Fuchs S., Satler L., Kornowski R., Okubagzi P., Weisz G., Baffour R., Waksman R., Weissman N., Cerqueira M., Leon M., and Epstein S. Catheter-based autologous bone marrow myocardial injection in no-option patients with advanced coronary artery disease: a feasibility study. J Am Coll Cardiol 41 (2003) 1721-1724
5. Wollert K., Meyer G., Lotz J., Ringes-Lichtenberg S., Lippolt P., Breidenbach C., Fichtner S., Korte T., Hornig B., Messinger D., Arseniev L., Hertenstein B., Ganser A., and Drexler H. Intracoronary autologous bone-marrow cell transfer after myocardial infarction: the BOOST randomised controlled clinical trial. Lancet 364 (2004) 141-148
6. Taylor D., Atkins B., Hungspreugs P., Jones T., Reedy M., Hutcheson K., Glower D., and Kraus W. Regenerating functional myocardium: improved performance after skeletal myoblast transplantation. Nat Med 4 (1998) 929-933
7. Menasche P., Hagege A., Scorsin M., Pouzet B., Desnos M., Duboc D., Schwartz K., Vilquin J., and Marolleau J. Myoblast transplantation for heart failure. Lancet 357 27 (2001) 279-280
8. +-enriched cell population into cardiomyocytes, endothelial cells, and smooth muscle cells in vivo. Circulation 108 (2003) 2070-2073
9. Soukiasian H., Czer L., Avital I., Aoki T., Kim Y., Umehara Y., Pass J., Tabrizi R., Magliato K., Fontana G., Cheng W., Demetriou A., and Trento A. A novel sub-population of bone marrow-derived myocardial stem cells: potential autologous cell therapy in myocardial infarction. J Heart Lung Transplant 23 (2004) 873-880
10. Ziegelhoeffer T., Fernandez B., Kostin S., Heil M., Voswinckel R., Helisch A., and Schaper W. Bone marrow-derived cells do not incorporate into the adult growing vasculature. Circ Res 94 (2004) 230-238
11. Fukuhara S., Tomita S., Nakatani T., Yutani C., and Kitamura S. Endogenous bone-marrow-derived stem cells contribute only a small proportion of regenerated myocardium in the acute infarction model. J Heart Lung Transplant 24 (2005) 67-72
12. Kinnaird T., Stabile E., Burnett M., and Epstein S. Bone-marrow-derived cells for enhancing collateral development: mechanisms, animal data, and initial clinical experiences. Circ Res 95 (2004) 354-363
13. Heil M., Ziegelhoeffer T., Mees B., and Schaper W. A different outlook on the role of bone marrow stem cells in vascular growth: bone marrow delivers software not hardware. Circ Res 94 (2004) 573-574
14. Dai W., Hale S., Martin B., Kuang J., Dow J., Wold L., and Kloner R. Allogeneic mesenchymal stem cell transplantation in postinfarcted rat myocardium: short- and long-term effects. Circulation 112 (2005) 214-223
15. Beltrami A., Urbanek K., Kajstura J., Yan S., Finato N., Bussani R., Nadal-Ginard B., Silvestri F., Leri A., Beltrami C., and Anversa P. Evidence that human cardiac myocytes divide after myocardial infarction. N Engl J Med 344 (2001) 1750-1757
16. Kajstura J., Leri A., Finato N., Di Loreto C., Beltrami C., and Anversa P. Myocyte proliferation in end-stage cardiac failure in humans. Proc Natl Acad Sci U S A 95 (1998) 8801-8805
17. Iwase T., Nagaya N., Fujii T., Itoh T., Murakami S., Matsumoto T., Kangawa K., and Kitamura S. Comparison of angiogenic potency between mesenchymal stem cells and mononuclear cells in a rat model of hindlimb ischemia. Cardiovasc Res 66 (2005) 543-551
18. Carvalho K., Guarita-Souza L., Rebelatto C., Senegaglia A., Hansen P., Mendonca J., Cury C., Francisco J., and Brofman P. Could the coculture of skeletal myoblasts and mesenchymal stem cells be a solution for postinfarction myocardial scar?. Transplant Proc 36 (2004) 991-992
19. Ott H., Bonaros N., Marksteiner R., Wolf D., Margreiter E., Schachner T., Laufer G., and Hering S. Combined transplantation of skeletal myoblasts and bone marrow stem cells for myocardial repair in rats. Eur J Cardiothorac Surg 25 (2004) 627-634
20. Laguens R., Cabeza Meckert P., Vera Janavel G., Del Valle H., Lascano E., Negroni J., Werba P., Cuniberti L., Martinez V., Melo C., Papouchado M., Ojeda R., Criscuolo M., and Crottogini A. Entrance in mitosis of adult cardiomyocytes in ischemic pig hearts after plasmid-mediated rhVEGF165 gene transfer. Gene Ther 9 (2002) 1676-1681
21. Kardami E. Stimulation and inhibition of cardiac myocyte proliferation in vitro. Mol Cell Biochem 92 (1990) 129-135
22. Sundgren N., Giraud G., Schultz J., Lasarev M., Stork P., and Thornburg K. Extracellular signal-regulated kinase and phosphoinositol-3 kinase mediate IGF-1 induced proliferation of fetal sheep cardiomyocytes. Am J Physiol Regul Integr Comp Physiol 285 (2003) R1481-R1489
23. Hamamoto M., Tomita S., Nakatani T., Yutani C., Yamashiro S., Sueda T., Yagihara T., and Kitamura S. Granulocyte-colony stimulating factor directly enhances proliferation of human troponin I-positive cells derived from idiopathic dilated cardiomyopathy through specific receptors. J Heart Lung Transplant 23 (2004) 1430-1437
24. Halevy O., and Cantley L. Differential regulation of the phosphoinositide 3-kinase and MAP kinase pathways by hepatocyte growth factor vs. insulin-like growth factor-I in myogenic cells. Exp Cell Res 297 (2004) 224-234
25. Foulstone E., Huser C., Crown A., Holly J., and Stewart C. Differential signaling mechanisms predisposing primary human skeletal muscle cells to altered proliferation and differentiation: roles of IGF-I and TNFalpha. Exp Cell Res 294 (2004) 223-235
26. Spangenburg E., and Booth F. Multiple signaling pathways mediate LIF-induced skeletal muscle satellite cell proliferation. Am J Physiol Cell Physiol 283 (2002) C204-C211
27. Rangappa S., Entwistle J., Wechsler A., and Kresh J. Cardiomyocyte-mediated contact programs human mesenchymal stem cells to express cardiogenic phenotype. J Thorac Cardiovasc Surg 126 (2003) 124-132
28. Matsusaka T., Katori H., Inagami T., Fogo A., and Ichikawa I. Communication between myocytes and fibroblasts in cardiac remodeling in angiotensin chimeric mice. J Clin Invest 103 (1999) 1451-1458
29. Formigli L., Francini F., Tani A., Squecco R., Nosi D., Polidori L., Nistri S., Chiappini L., Cesati V., Pacini A., Perna A., Orlandini G., Zecchi Orlandini S., and Bani D. Morphofunctional integration between skeletal myoblasts and adult cardiomyocytes in coculture is favored by direct cell-cell contacts and relaxin treatment. Am J Physiol Cell Physiol 288 (2005) C795-C804