Tenascin C may regulate the recruitment of smooth muscle cells during coronary artery development

Differentiation

Volumn 81, Issue 5, 2011, Pages 299-306

  Ando, Katsumi ^a   Takahashi, Makiko ^b   Yamagishi, Toshiyuki ^b   Miyagawa Tomita, Sachiko ^c   Imanaka Yoshida, Kyoko ^d,e   Yoshida, Toshimichi ^d,e   Nakajima, Yuji ^b  

^a SAITAMA PREFECTURAL UNIVERSITY   (Japan)

^b OSAKA CITY UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^c TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^d MIE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^e MIE UNIVERSITY   (Japan)

Author keywords

Avian heart; Coronary vessel development; Smooth muscle cell; Tenascin C

Indexed keywords

ALPHA SMOOTH MUSCLE ACTIN; NEUTRALIZING ANTIBODY; TENASCIN;

ANGIOGENESIS; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CHICK; CHIMERA; CONTROLLED STUDY; CORONARY ARTERY; EMBRYO; EMBRYO PATTERN FORMATION; ENDOTHELIUM CELL; HEART; HEART DEVELOPMENT; HEART MUSCLE CELL; MYOFIBROBLAST; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROEPICARDIAL ORGAN; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; QUAIL; SMOOTH MUSCLE FIBER;

ACTINS; ANIMALS; CELL CULTURE TECHNIQUES; CELL DIFFERENTIATION; CHICK EMBRYO; CORONARY VESSELS; HEART; IMMUNOHISTOCHEMISTRY; MUSCLE DEVELOPMENT; MUSCLE, SMOOTH, VASCULAR; ORGANOGENESIS; PERICARDIUM; QUAIL; TENASCIN;

AVES; PHASIANIDAE;

EID: 79958134271     PISSN: 03014681     EISSN: 14320436     Source Type: Journal    
DOI: 10.1016/j.diff.2011.03.002     Document Type: Article

References (51)

1. Ando K., Nakajima Y., Yamagishi T., Yamamoto S., Nakamura H. Development of proximal coronary arteries in quail embryonic heart: multiple capillaries penetrating the aortic sinus fuse to form main coronary trunk. Circ. Res. 2004, 94:346-352.
2. Ballard V.L.T., Sharma A., Duignan I., Holm J.M., Chin A., Choi R., Hajjar K.A., Wong S.-C., Edelberg J.M. Vascular tenascin-c regulates cardiac endothelial phenotype and neovascularization. FASEB J. 2006, 20:717-719.
3. Bogers A.J.J.C., Gittenberger-de, Groot A.C., Poelmann R.E., Péault B.M., Huysmans H.A. Development of the origin of the coronary arteries, a matter of ingrowth or outgrowth?. Anat. Embryol. 1989, 180:437-441.
4. Castellon R., Caballero S., Hamdi H.K., Atilano S.R., Aoki A.M., Tarnuzzer R.W., Kenney M.C., Grant M.B., Ljubimov A.V. Effects of tenascin-C on normaland diabetic retinal endothelial cells in culture. Invest. Ophthalmol. Vis. Sci. 2002, 43:2758-2766.
5. Compton L.A., Potash D.A., Mundell N.A., Barnett J.V. Transforming growth factor-Β induces loss of epithelial character and smooth muscle cell differentiation in epicardial cells. Dev. Dyn. 2006, 235:82-93.
6. Crossin K.L., Hoffman S. Expression of adhesion molecules during the formation and differentiation of the avian endocardial cushion tissue. Dev. Biol. 1991, 145:277-286.
7. Gurevicius K., Kuang F., Stoenica L., Irintchev A., Gureviciene I., Dityatev A., Schachner M., Tanila H. Genetic ablation of tenascin-C expression leads to abnormal hippocampal CA1 structure and electrical activity in vivo. Hippocampus 2009, 19:1232-1246.
8. Hamburger V., Hamilton H.L. A series of normal stages in the development of the chick embryo. Dev. Dyn. 1992, 195:231-272.
9. Hellström M., Kalén M., Lindahl P., Abramsson A., Betsholtz C. Role of PDGF-B and PDGFR-beta in recruitment of vascular smooth muscle cells and pericytes during embryonic blood vessel formation in the mouse. Development 1999, 126:3047-3055.
10. Hirakow R. Development of the cardiac blood vessels in staged human embryos. Acta. Anat 1983, 115:220-230.
11. Hiruma T., Hirakow R. Epicardial formation in embryonic chick heart: computer-aided reconstruction, scanning, and transmission electron microscopic studies. Am. J. Anat. 1989, 184:129-138.
12. Hurle J.M., Garcia-Martinez V., Ros M.A. Immunofluorescent localization of tenascin during the morphogenesis of the outflow tract of the chick embryo heart. Anat. Embryol. 1990, 181:149-155.
13. Imanaka-Yoshida K., Hiroe M., Nishikawa T., Ishiyama S., Shimojo T., Ohta Y., Sakakura T., Yoshida T. Tenascin-C modulates adhesion of cardiomyocytes to extracellular matrix during tissue remodeling after myocardial infarction. Lab. Invest. 2001, 81:1015-1024.
14. Imanaka-Yoshida K., Matsuura R., Isaka N., Nakano T., Sakakura T., Yoshida T. Serial extracellular matrix changes in neointimal lesions of human coronary artery after percutaneous transluminal coronary angioplasty: clinical significance of early tenascin-C expression. Virchows. Arch. 2001, 439:185-190.
15. Imanaka-Yoshida K., Matsumoto K., Hara M., Sakakura T., Yoshida T. The dynamic expression of tenascin-C and tenascin-X during early heart development in the mouse. Differentiation 2003, 71:291-298.
16. Imanaka-Yoshida K., Hiroe M., Yoshida T. Interaction between cell and extracellular matrix in heart disease: multiple roles of tenascin-C in tissue remodeling. Histol. Histopathol. 2004, 19:517-525.
17. Ishii K., Imanaka-Yoshida K., Yoshida T., Sugimura Y. Role of stromal tenascin-C in mouse prostatic development and epithelial cell differentiation. Dev. Biol. 2008, 324:310-319.
18. Ishii Y., Langberg J., Rosborough K., Mikawa T. Endothelial cell lineages of the heart. Cell Tissue Res. 2009, 335:67-73.
19. Ishigaki, T., Imanaka-Yoshida, K., Shimojo, N., Matsushima, S., Taki, W., Yoshida, T.. Tenascin-C enhances crosstalk signaling of integrin αvΒ3/PDGFR-Β complex by SRC recruitment promoting PDGF-induced proliferation and migration in smooth muscle cells. J. Cell Physiol.. (Epub ahead).
20. Jallo G.I., Friedlander D.R., Kelly P.J., Wisoff J.H., Grumet M., Zagzag D. Tenascin-C expression in the cyst wall and fluid of human brain tumors correlates with angiogenesis. Neurosurgery 1997, 41:1052-1059.
21. Jiang X., Rowitch D.H., Soriano P., McMahon A.P., Sucov H.M. Fate of the mammalian cardiac neural crest. Development 2000, 127:1607-1616.
22. Jones F.S., Jones P.L. The tenascin family of ECM glycoproteins: Structure, function, and regulation during embryonic development and tissue remodeling. Dev. Dyn. 2000, 218:235-259.
23. Kataoka H., Takakura N., Nishikawa S., Tsuchida K., Kodama H., Kunisada T., Risau W., Kita T., Nishikawa S.I. Expressions of PDGF receptor alpha, c-Kit and Flk1 genes clustering in mouse chromosome 5 define distinct subsets of nascent mesodermal cells. Dev. Growth Differ 1997, 39:729-740.
24. Kattan J., Dettman R.W., Bristow J. Formation and remodeling of the coronary vascular bed in the embryonic avian heart. Dev. Dyn. 2004, 230:34-43.
25. Landerholm T.E., Dong X.R., Lu J., Belaguli N.S., Schwartz R.J., Majesky M.W. A role for serum response factor in coronary smooth muscle differentiation from proepicardial cells. Development 1999, 126:2053-2062.
26. Männer J. Does the subepicardial mesenchyme contribute myocardioblasts to the myocardium of the chick embryo heart? A quail-chick chimera study tracing the fate of the epicardial primordium. Anat. Rec. 1999, 255:212-226.
27. Matsui H., Sakabe M., Sakata H., Yanagawa N., Ikeda K., Yamagishi T., Nakajima Y. Induction of initial heart -actin, smooth muscle -αctin, in chick pregastrula epiblast: The role of hypoblast and fibroblast growth factor-8. Dev. Growth. Differ. 2008, 50:143-157.
28. Mellgren A.M., Smith C.L., Olsen G.S., Eskiocak B., Zhou B., Kazi M.N., Ruiz F.R., Pu W.T., Tallquist M.D. Platelet-derived growth factor receptor Β signaling is required for efficient epicardial cell migration and development of two distinct coronary vascular smooth muscle Cell populations. Circ. Res. 2008, 103:1393-1401.
29. Metzger R.J., Klein O.D., Martin G.R., Krasnow M.A. The branching programme of mouse lung development. Nature 2008, 453:733-735.
30. Midwood K.S., Orend G. The role of tenascin-C in tissue injury and tumorigenesis. J. Cell Commun. Signal 2009, 3:287-310.
31. Mikawa T., Gourdie R.G. Pericardial mesoderm generates a population of coronary smooth muscle cells migrating into the heart along with ingrowth of the epicardial organ. Dev. Biol. 1996, 174:221-232.
32. Mu H., Ohashi R., Lin P., Yao Q., Chen C. Cellular and molecular mechanisms of coronary vessel development. Vasc. Med. 2005, 10:37-44.
33. Nahirney P.C., Mikawa T., Fischman D.A. Evidence for an extracellular matrix bridge guiding proepicardial cell migration to the myocardium of chick embryos. Dev. Dyn. 2003, 227:511-523.
34. Nishioka T., Onishi K., Shimojo N., Nagano Y., Matsusaka H., Ikeuchi M., Ide T., Tsutsui H., Hiroe M., Yoshida T., Imanaka-Yoshida K. Tenascin-C may aggravate left ventricular remodeling and function after myocardial infarction in mice. Am. J. Physiol. Heart Circ. Physiol. 2010, 298:H1072-H1078.
35. Olivey H.E., Compton L.A., Barnett J.V. Coronary vessel development: the epicardium delivers. Trends. Cardiovasc. Med. 2004, 14:247-251.
36. Paik D.C., Fu C., Bhattacharya J., Tilson M.D. Ongoing angiogenesis in blood vessels of the abdominal aortic aneurysm. Exp. Mol. Med. 2004, 36:524-533.
37. Poelmann R.E., Gittenberger-de, Groot A.C., Mentink M.M., Bokenkamp R., Hogers B. Development of the cardiac coronary vascular endothelium, studied with antiendothelial antibodies, in chicken-quail chimeras. Circ. Res. 1993, 73:559-568.
38. Ratajska A., Czarnowska E., Ciszek B. Embryonic development of the proepicardium and coronary vessels. Int. J. Dev. Biol. 2008, 52:229-236.
39. Red-Horse K., Ueno H., Weissman I.L., Krasnow M.A. Coronary arteries form by developmental reprogramming of venous cells. Nature 2010, 464:549-553.
40. Reese D.E., Mikawa T., Bader D.M. Development of the coronary vessel system. Circ. Res. 2002, 91:761-768.
41. Saga Y., Yagi T., Ikawa Y., Sakakura T., Aizawa S. Mice develop normally without tenascin. Genes Dev. 1992, 6:1821-1831.
42. Tamaoki M., Imanaka-Yoshida K., Yokoyama K., Nishioka T., Inada H., Hiroe M., Sakakura T., Yoshida T. Tenascin-C regulates recruitment of myofibroblasts during tissue repair after myocardial injury. Am. J. Pathol. 2005, 167:71-80.
43. Tanaka K., Hiraiwa N., Hashimoto H., Yamazaki Y., Kusakabe M. Tenascin-C regulates angiogenesis in tumor through the regulation of vascular endothelial growth factor expression. Int. J. Cancer 2004, 108:31-40.
44. Tucker R.P., Chiquet-Ehrismann R. The regulation of tenascin expression by tissue microenvironments. Biochim. Biophys. Acta 2009, 1793:888-892.
45. Sugi Y., Markwald R.R. Formation and early morphogenesis of endocardial endothelial precursor cells and the role of endoderm. Dev. Biol. 1996, 175:66-83.
46. Van Den Akker N.M.S., Lie-Venema H., Maas S., Eralp I., DeRuiter M.C., Poelmann R.E., Gittenberger-De, Groot A.C. Platelet-derived growth factors in the developing avian heart and maturating coronary vasculature. Dev. Dyn. 2005, 233:1579-1588.
47. Waldo K.L., Willner W., Kirby M.L. Origin of the proximal coronary artery stems and a review of ventricular vascularization in the chick embryo. Am. J. Anat. 1990, 188:109-120.
48. Verzi M.P., McCulley D.J., De Val S., Dodou E., Black B.L. The right ventricle, outflow tract, and ventricular septum comprise a restricted expression domain within the secondary/anterior heart field. Dev. Biol. 2005, 287:134-145.
49. Vrancken Peeters M.-P.F.M., Gittenberger-de, Groot A.C., Mentink M.M.T., Hungerford J.E., Little C.D., Poelmann R.E. The development of the coronary vessels and their differentiation into arteries and veins in the embryonic quail heart. Dev. Dyn. 1997, 208:338-348.
50. Zagzag D., Shiff B., Jallo G.I., Greco M.A., Blanco C., Cohen H., Hukin J., Allen J.C., Fridlander D.R. Tenascin-C promotes microvascular cell migration and phosphorylation of focal adhesion kinase. Cancer Res. 2002, 62:2660-2668.
51. Zhang H.Y., Kluge M., Timpl R., Chu M.L., Ekblom P. The extracellular matrix glycoproteins BM-90 and tenascin are expressed in the mesenchyme at sites of endothelial-mesenchymal conversion in the embryonic mouse heart. Differentiation 2006, 52:211-220.