Identification of a novel developmental mechanism in the generation of mesothelia

Development (Cambridge)

Volumn 139, Issue 16, 2012, Pages 2926-2934

  Winters, Nichelle I ^a   Thomason, Rebecca T ^a   Bader, David M ^a,b  

^a VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VANDERBILT UNIVERSITY   (United States)

Author keywords

Chick; Intestine; Mesothelium; Quail; Splanchnic mesoderm

Indexed keywords

ANIMAL CELL; ARTICLE; CELL LINE; CELL LINEAGE; CELL MATURATION; CHICK; CHIMERA; COELOMATA; EMBRYO; EPICARDIUM; INTESTINE EPITHELIUM CELL; MESOTHELIUM CELL; MORPHOGENESIS; NONHUMAN; PRIMORDIUM; PRIORITY JOURNAL; QUAIL; STEM CELL;

ANIMALS; ANIMALS, GENETICALLY MODIFIED; CELL LINEAGE; CHICK EMBRYO; COTURNIX; EMBRYONIC STEM CELLS; EPITHELIAL CELLS; EPITHELIUM; GREEN FLUORESCENT PROTEINS; INTESTINES; RECOMBINANT PROTEINS; TRANSPLANTATION CHIMERA;

PHASIANIDAE;

EID: 84864297906     PISSN: 09501991     EISSN: 14779129     Source Type: Journal    
DOI: 10.1242/dev.082396     Document Type: Article

References (43)

1. Acencio, M. M., Vargas, F. S., Marchi, E., Carnevale, G. G., Teixeira, L. R., Antonangelo, L. and Broaddus, V. C. (2007). Pleural mesothelial cells mediate inflammatory and profibrotic responses in talc-induced pleurodesis. Lung 185, 343-348.
2. Aroeira, L. S., Aguilera, A., Selgas, R., Ramírez-Huesca, M., Pérez-Lozano, M. L., Cirugeda, A., Bajo, M. A., del Peso, G., Sánchez-Tomero, J. A., Jiménez-Heffernan, J. A. et al. (2005). Mesenchymal conversion of mesothelial cells as a mechanism responsible for high solute transport rate in peritoneal dialysis: role of vascular endothelial growth factor. Am. J. Kidney Dis. 46, 938-948.
3. Asahina, K., Zhou, B., Pu, W. T. and Tsukamoto, H. (2011). Septum transversum-derived mesothelium gives rise to hepatic stellate cells and perivascular mesenchymal cells in developing mouse liver. Hepatology 53, 983-995.
4. Braun, N., Alscher, D. M., Fritz, P., Edenhofer, I., Kimmel, M., Gaspert, A., Reimold, F., Bode-Lesniewska, B., Ziegler, U., Biegger, D. et al. (2011). Podoplanin-positive cells are a hallmark of encapsulating peritoneal sclerosis. Nephrol. Dial. Transplant. 26, 1033-1041.
5. Chegini, N. (2008). TGF-beta system: the principal profibrotic mediator of peritoneal adhesion formation. Semin. Reprod. Med. 26, 298-312.
6. Decologne, N., Kolb, M., Margetts, P. J., Menetrier, F., Artur, Y., Garrido, C., Gauldie, J., Camus, P. and Bonniaud, P. (2007). TGF-beta1 induces progressive pleural scarring and subpleural fibrosis. J. Immunol. 179, 6043-6051.
7. Dettman, R. W., Denetclaw, W., Jr, Ordahl, C. P. and Bristow, J. (1998). Common epicardial origin of coronary vascular smooth muscle, perivascular fibroblasts, and intermyocardial fibroblasts in the avian heart. Dev. Biol. 193, 169-181.
8. Devuyst, O., Margetts, P. J. and Topley, N. (2010). The pathophysiology of the peritoneal membrane. J. Am. Soc. Nephrol. 21, 1077-1085.
9. Eralp, I., Lie-Venema, H., DeRuiter, M. C., van den Akker, N. M., Bogers, A. J., Mentink, M. M., Poelmann, R. E. and Gittenberger-de Groot, A. C. (2005). Coronary artery and orifice development is associated with proper timing of epicardial outgrowth and correlated Fas-ligand-associated apoptosis patterns. Circ. Res. 96, 526-534.
10. Gittenberger-de Groot, A. C., Vrancken Peeters, M. P., Bergwerff, M., Mentink, M. M. and Poelmann, R. E. (2000). Epicardial outgrowth inhibition leads to compensatory mesothelial outflow tract collar and abnormal cardiac septation and coronary formation. Circ. Res. 87, 969-971.
11. Hamburger, V. and Hamilton, H. L. (1992). A series of normal stages in the development of the chick embryo. 1951. Dev. Dyn. 195, 231-272.
12. Ho, E. and Shimada, Y. (1978). Formation of the epicardium studied with the scanning electron microscope. Dev. Biol. 66, 579-585.
13. Ishii, Y., Langberg, J. D., Hurtado, R., Lee, S. and Mikawa, T. (2007). Induction of proepicardial marker gene expression by the liver bud. Development 134, 3627-3637.
14. Ishii, Y., Garriock, R. J., Navetta, A. M., Coughlin, L. E. and Mikawa, T. (2010). BMP signals promote proepicardial protrusion necessary for recruitment of coronary vessel and epicardial progenitors to the heart. Dev. Cell 19, 307-316.
15. Kawaguchi, M., Bader, D. M. and Wilm, B. (2007). Serosal mesothelium retains vasculogenic potential. Dev. Dyn. 236, 2973-2979.
16. King, T. E., Jr, Pardo, A. and Selman, M. (2011). Idiopathic pulmonary fibrosis. Lancet 378, 1949-1961.
17. Kruithof, B. P., van Wijk, B., Somi, S., Kruithof-de Julio, M., Pérez Pomares, J. M., Weesie, F., Wessels, A., Moorman, A. F. and van den Hoff, M. J. (2006). BMP and FGF regulate the differentiation of multipotential pericardial mesoderm into the myocardial or epicardial lineage. Dev. Biol. 295, 507-522.
18. Lassiter, R. N., Dude, C. M., Reynolds, S. B., Winters, N. I., Baker, C. V. and Stark, M. R. (2007). Canonical Wnt signaling is required for ophthalmic trigeminal placode cell fate determination and maintenance. Dev. Biol. 308, 392-406.
19. Manasek, F. J. (1969). Embryonic development of the heart. II. Formation of the epicardium. J. Embryol. Exp. Morphol. 22, 333-348.
20. Männer, J., Schlueter, J. and Brand, T. (2005). Experimental analyses of the function of the proepicardium using a new microsurgical procedure to induce loss-of-proepicardial-function in chick embryos. Dev. Dyn. 233, 1454-1463.
21. McGlinn, E. and Mansfield, J. H. (2011). Detection of gene expression in mouse embryos and tissue sections. Methods Mol. Biol. 770, 259-292.
22. Mikawa, T. and Gourdie, R. G. (1996). Pericardial mesoderm generates a population of coronary smooth muscle cells migrating into the heart along with ingrowth of the epicardial organ. Dev. Biol. 174, 221-232.
23. Minot, C.-S. (1890). The mesoderm and the coelom of vertebrates. Am. Nat. 24, 877-898.
24. Moore, K. L. and Persaud, T. V. N. (1998). The Developing Human: Clinically Oriented Embryology. Philadelphia: Saunders.
25. Morimoto, M., Liu, Z., Cheng, H. T., Winters, N., Bader, D. and Kopan, R. (2010). Canonical Notch signaling in the developing lung is required for determination of arterial smooth muscle cells and selection of Clara versus ciliated cell fate. J. Cell Sci. 123, 213-224.
26. Mutsaers, S. E. (2002). Mesothelial cells: their structure, function and role in serosal repair. Respirology 7, 171-191.
27. Mutsaers, S. E. and Wilkosz, S. (2007). Structure and function of mesothelial cells. Cancer Treat. Res. 134, 1-19.
28. Mutsaers, S. E., Prele, C. M., Brody, A. R. and Idell, S. (2004). Pathogenesis of pleural fibrosis. Respirology 9, 428-440.
29. Osler, M. E. and Bader, D. M. (2004). Bves expression during avian embryogenesis. Dev. Dyn. 229, 658-667.
30. Pérez-Pomares, J. M., Carmona, R., González-Iriarte, M., Macías, D., Guadix, J. A. and Muñoz-Chápuli, R. (2004). Contribution of mesothelium-derived cells to liver sinusoids in avian embryos. Dev. Dyn. 229, 465-474.
31. Que, J., Wilm, B., Hasegawa, H., Wang, F., Bader, D. and Hogan, B. L. (2008). Mesothelium contributes to vascular smooth muscle and mesenchyme during lung development. Proc. Natl. Acad. Sci. USA 105, 16626-16630.
32. Schlueter, J., Männer, J. and Brand, T. (2006). BMP is an important regulator of proepicardial identity in the chick embryo. Dev. Biol. 295, 546-558.
33. Schulte, I., Schlueter, J., Abu-Issa, R., Brand, T. and Männer, J. (2007). Morphological and molecular left-right asymmetries in the development of the proepicardium: a comparative analysis on mouse and chick embryos. Dev. Dyn. 236, 684-695.
34. Shelton, E. L., Poole, S. D., Reese, J. and Bader, D. M. (2012). Omental grafting: a cell-based therapy for blood vessel repair. J. Tissue Eng. Regen. Med. doi: 10.1002/term.528.
35. Takaba, K., Jiang, C., Nemoto, S., Saji, Y., Ikeda, T., Urayama, S., Azuma, T., Hokugo, A., Tsutsumi, S., Tabata, Y. et al. (2006). A combination of omental flap and growth factor therapy induces arteriogenesis and increases myocardial perfusion in chronic myocardial ischemia: evolving concept of biologic coronary artery bypass grafting. J. Thorac. Cardiovasc. Surg. 132, 891-899.
36. Venters, S. J., Dias da Silva, M. R. and Hyer, J. (2008). Murine retroviruses reengineered for lineage tracing and expression of toxic genes in the developing chick embryo. Dev. Dyn. 237, 3260-3269.
37. Wilm, B., Ipenberg, A., Hastie, N. D., Burch, J. B. and Bader, D. M. (2005). The serosal mesothelium is a major source of smooth muscle cells of the gut vasculature. Development 132, 5317-5328.
38. Wu, M., Smith, C. L., Hall, J. A., Lee, I., Luby-Phelps, K. and Tallquist, M. D. (2010). Epicardial spindle orientation controls cell entry into the myocardium. Dev. Cell 19, 114-125.
39. Yáñez-Mó, M., Lara-Pezzi, E., Selgas, R., Ramírez-Huesca, M., Domínguez-Jiménez, C., Jiménez-Heffernan, J. A., Aguilera, A., Sánchez-Tomero, J. A., Bajo, M. A., Alvarez, V. et al. (2003). Peritoneal dialysis and epithelial-tomesenchymal transition of mesothelial cells. N. Engl. J. Med. 348, 403-413.
40. Yung, S. and Chan, T. M. (2009). Intrinsic cells: mesothelial cells - central players in regulating inflammation and resolution. Perit. Dial. Int. 29 Suppl. 2, S21-S27.
41. Zhang, Q. X., Magovern, C. J., Mack, C. A., Budenbender, K. T., Ko, W. and Rosengart, T. K. (1997). Vascular endothelial growth factor is the major angiogenic factor in omentum: mechanism of the omentum-mediated angiogenesis. J. Surg. Res. 67, 147-154.
42. Zhou, B. and Pu, W. T. (2011). Epicardial epithelial-to-mesenchymal transition in injured heart. J. Cell. Mol. Med. 15, 2781-2783.
43. Zhou, B., Honor, L. B., He, H., Ma, Q., Oh, J. H., Butterfield, C., Lin, R. Z., Melero-Martin, J. M., Dolmatova, E., Duffy, H. S. et al. (2011). Adult mouse epicardium modulates myocardial injury by secreting paracrine factors. J. Clin. Invest. 121, 1894-1904.