Metamorphosis of mesothelial cells with active horizontal motility in tissue culture

Scientific Reports

Volumn 3, Issue , 2013, Pages

  Nagai, Hirotaka ^a   Chew, Shan Hwu ^a   Okazaki, Yasumasa ^a   Funahashi, Satomi ^a   Namba, Takashi ^a   Kato, Takuya ^a   Enomoto, Atsushi ^a   Jiang, Li ^a   Akatsuka, Shinya ^a   Toyokuni, Shinya ^a  

^a NAGOYA UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; APOPTOSIS; ARTICLE; CELL HYPOXIA; CELL LINE; CELL MOTION; CULTURE TECHNIQUE; CYTOLOGY; EPITHELIUM CELL; METABOLISM; MOUSE; TRANSCELLULAR CELL MIGRATION; ULTRASTRUCTURE;

ANIMALS; APOPTOSIS; CELL CULTURE TECHNIQUES; CELL HYPOXIA; CELL LINE; CELL MOVEMENT; EPITHELIAL CELLS; MICE; TRANSCELLULAR CELL MIGRATION;

MLCS; MLOWN;

EID: 84873118296     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep01144     Document Type: Article

References (33)

1. Mutsaers, S. E. Mesothelial cells: their structure, function and role in serosal repair. Respirology 7, 171-191 (2002).
2. Herrick, S. E. & Mutsaers, S. E. Mesothelial progenitor cells and their potential in tissue engineering. Int. J. Biochem. Cell Biol. 36, 621-642 (2004). (Pubitemid 38316819)
3. Andrews, P. M. & Porter, K. R. The ultrastructural morphology and possible functional significance of mesothelial microvilli. Anat. Rec. 177, 409-426 (1973).
4. Fedorko, M. E. & Hirsch, J. G. Studies on transport of macromolecules and small particles across mesothelial cells of the mouse omentum. I. Morphologic aspects. Exp. Cell Res. 69, 113-127 (1971).
5. Yung, S. & Chan, T. M. Intrinsic cells: mesothelial cells-central players in regulating inflammation and resolution. Perit. Dial. Int. 29 Suppl 2, S21-27 (2009).
6. Van Der Wal, B. C., Hofland, L. J. Marquet, R. L., Van Koetsveld, P. M., Van Rossen, M. E. & Van Eijck, C.H. Paracrine interactions between mesothelial and colon-carcinoma cells in a rat model. Int. J. Cancer 73, 885-890 (1997). (Pubitemid 127483046)
7. Hu, Q., Akatsuka, S., Yamashita, Y., Ohara, H., Nagai, H., Okazaki, Y., Takahashi, T. & Toyokuni, S. Homozygous deletion of CDKN2A/2B is a hallmark of iron-induced high-grade rat mesothelioma. Lab. Invest. 90, 360-373 (2010).
8. Nagai, H., Okazaki, Y., Chew, S. H., Misawa, N., Yamashita, Y., Akatsuka, S., Ishihara, T., Yamashita, K., Yoshikawa, Y., Yasui, H., Jiang, L., Ohara, H., Takahashi, T., Ichihara, G., Kostarelos, K., Miyata, Y., Shinohara, H. & Toyokuni, S. Diameter and rigidity of multiwalled carbon nanotubes are critical factors in mesothelial injury and carcinogenesis. Proc. Natl. Acad. Sci. USA 108, E1330-1338 (2011).
9. Akatsuka, S., Yamashita, Y.,Ohara, H., Liu, Y. T., Izumiya, M.,Abe, K.,Ochiai, M., Jiang, L., Nagai, H., Okazaki, Y., Murakami, H., Sekido, Y., Arai, E., Kanai, Y., Hino, O., Takahashi, T., Nakagama, H. & Toyokuni, S. Fenton reaction induced cancer in wild type rats recapitulates genomic alterations observed in human cancer. PLoS One 7, e43403 (2012).
10. Jiang, L., Akatsuka, S., Nagai, H., Chew, S. H., Ohara, H., Okazaki, Y., Yamashita, Y., Yoshikawa, Y., Yasui, H., Ikuta, K., Sasaki, K., Kohgo, Y., Hirano, S., Shinohara, Y., Kohyama, N., Takahashi, T. & Toyokuni, S. Iron overload signature in chrysotile-induced malignant mesothelioma. J. Pathol. 228, 366-377 (2012).
11. Nagai, H. & Toyokuni, S. Differences and similarities between carbon nanotubes and asbestos fibers during mesothelial carcinogenesis: shedding light on fiber entry mechanism. Cancer Sci. 103, 1378-1390 (2012).
12. Dobbie, J. W., Zaki, M. & Wilson, L. Ultrastructural studies on the peritoneum with special reference to chronic ambulatory peritoneal dialysis. Scott. Med. J. 26, 213-223 (1981). (Pubitemid 11009121)
13. Di Paolo, S., Gesualdo, L., Ranieri, E., Grandaliano, G. & Schena, F. P. High glucose concentration induces the overexpression of transforming growth factor-beta through the activation of a platelet-derived growth factor loop in human mesangial cells. Am. J. Pathol. 149, 2095-2106 (1996). (Pubitemid 26415226)
14. Ellis, H. The cause and prevention of postoperative intraperitoneal adhesions. Surg. Gynecol. Obstet. 133, 497-511 (1971).
15. Nagai, H. & Toyokuni, S. Biopersistent fiber-induced inflammation and carcinogenesis: lessons learned from asbestos toward safety of fibrous nanomaterials. Arch. Biochem. Biophys. 502, 1-7 (2010).
16. Mutsaers, S. E., Whitaker, D. & Papadimitriou, J. M. Mesothelial regeneration is not dependent on subserosal cells. J. Pathol. 190, 86-92 (2000). (Pubitemid 30053358)
17. Whitaker, D. & Papadimitriou, J. Mesothelial healing: morphological and kinetic investigations. J. Pathol. 145, 159-175 (1985). (Pubitemid 15138587)
18. Ryan, G. B., Grobety, J. & Majno, G. Mesothelial injury and recovery. Am. J. Pathol. 71, 93-112 (1973).
19. Foley-Comer, A. J., Herrick, S. E., Al-Mishlab, T., Prele, C. M., Laurent, G. J. & Mutsaers, S. E. Evidence for incorporation of free-floating mesothelial cells as a mechanism of serosal healing. J. Cell Sci. 115, 1383-1389 (2002). (Pubitemid 34428696)
20. Bolen, J.W., Hammar, S. P.&Mcnutt, M. A. Reactive and neoplastic serosal tissue. Alight-microscopic, ultrastructural, and immunocytochemical study. Am. J. Surg. Pathol. 10, 34-47 (1986). (Pubitemid 16108565)
21. Pampinella, F., Roelofs, M., Castellucci, E., Chiavegato, A., Guidolin, D., Passerini-Glazel, G., Pagano, F. & Sartore, S. Proliferation of submesothelial mesenchymal cells during early phase of serosal thickening in the rabbit bladder is accompanied by transient keratin 18 expression. Exp. Cell Res. 223, 327-339 (1996). (Pubitemid 26089090)
22. Mutsaers, S. E., Whitaker, D. & Papadimitriou, J. M. Stimulation of mesothelial cell proliferation by exudate macrophages enhances serosal wound healing in a murine model. Am. J. Pathol. 160, 681-692 (2002). (Pubitemid 34160346)
23. Fotev, Z., Whitaker, D.&Papadimitriou, J. M. Role of macrophages in mesothelial healing. J. Pathol. 151, 209-219 (1987). (Pubitemid 17066282)
24. Mutsaers, S. E. The mesothelial cell. Int. J. Biochem. Cell Biol. 36, 9-16 (2004). (Pubitemid 37338468)
25. Yap, A. S.&Kovacs, E. M. Direct cadherin-activated cell signaling: a view from the plasma membrane. J. Cell Biol. 160, 11-16 (2003). (Pubitemid 36091712)
26. Hazan, R. B., Qiao, R., Keren, R., Badano, I. & Suyama, K. Cadherin switch in tumor progression. Ann. N. Y. Acad. Sci. 1014, 155-163 (2004). (Pubitemid 38594801)
27. Hott, J. W., Sparks, J. A., Godbey, S. W. & Antony, V. B. Mesothelial cell response to pleural injury: thrombin-induced proliferation and chemotaxis of rat pleural mesothelial cells. Am. J. Respir. Cell Mol. Biol. 6, 421-425 (1992).
28. Nasreen, N., Mohammed, K. A., Galffy, G.,Ward,M. J. & Antony, V. B. MCP-1 in pleural injury: CCR2 mediates haptotaxis of pleural mesothelial cells. Am. J. Physiol.-Lung Cell. Mol. Physiol. 278, L591-598 (2000). (Pubitemid 30152517)
29. Strukova, S. M. Thrombin as a regulator of inflammation and reparative processes in tissues. Biochemistry (Mosc). 66, 8-18 (2001). (Pubitemid 33640786)
30. Shireman, P. K., Contreras-Shannon, V., Ochoa, O., Karia, B. P.,Michalek, J. E. & Mcmanus, L. M. MCP-1 deficiency causes altered inflammation with impaired skeletal muscle regeneration. J. Leukoc. Biol. 81, 775-785 (2007). (Pubitemid 46393555)
31. Topley, N., Brown, Z., Jorres, A., Westwick, J., Davies, M., Coles G.A. & Williams J.D. Human peritoneal mesothelial cells synthesize interleukin-8. Synergistic induction by interleukin-1 beta and tumor necrosis factor-alpha. Am. J. Pathol. 142, 1876-1886 (1993). (Pubitemid 24057082)
32. Topley, N., Jorres, A., Luttmann,W., Petersen, M. M., Lang, M. J. Thierauch, K.H., Muller, C., Coles, G. A., Davies, M. & Williams, J. D. Human peritoneal mesothelial cells synthesize interleukin-6: induction by IL-1 beta and TNF alpha. Kidney Int. 43, 226-233 (1993). (Pubitemid 23167470)
33. Eigenbrod, T., Park, J. H.,Harder, J., Iwakura, Y.&Nunez, G. Cutting edge: critical role for mesothelial cells in necrosis-induced inflammation through the recognition of IL-1 alpha released from dying cells. J. Immunol. 181, 8194-8198 (2008).