Nitric oxide is necessary for a switch from stationary to locomoting phenotype in epithelial cells

American Journal of Physiology - Cell Physiology

Volumn 270, Issue 3 39-3, 1996, Pages

  Noiri, Eisei ^b   Peresleni, Tatyana ^b   Srivastava, Neil ^b   Weber, Pamela ^b   Bahou, Wadie F ^b   Peunova, Natalia ^b   Goligorsky, Michael S ^a  

^a STONY BROOK UNIVERSITY   (United States)

^b NONE

Author keywords

epithelial wound healing; growth factors; migration

Indexed keywords

ANTISENSE OLIGODEOXYNUCLEOTIDE; EPIDERMAL GROWTH FACTOR; NITRIC OXIDE;

ANIMAL CELL; ARTICLE; CELL MIGRATION; CELL MOTILITY; CONTROLLED STUDY; EPITHELIUM CELL; MONOLAYER CULTURE; NONHUMAN; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; WOUND HEALING;

EID: 0029875343     PISSN: 03636143     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpcell.1996.270.3.c794     Document Type: Article

References (52)

1. Abererombie, M., J. E. M. Heaysman, and S. M. Pegrum. The locomotion of fibroblasts in culture. III. Movement of particles on the dorsal surface of the leading lamella. Exp. Cell Res. 62: 389-398, 1970.
2. Abererombie, M., J. E. M. Heaysman, and S. M. Pegrum. The locomotion of fihroblasts in culture. IV Electron microscopy of the leading lamella. Exp. Cell Res. 67: 359-367, 1971.
3. Abererombie, M., J. E. M. Heaysman, and S. M. Pegrum. The locomotion of fibroblasts in culture. V. Surface marking with concanavalin A. Exp. Cell Res. 73: 536-539, 1972.
4. Albina, J. E., C. D. Mills, A. Barbul, C. E. Thurkill, W. L. Henry, B. Mastrofrancesco, and M. D, Caldwell. Arginine metabolism in wounds. Am. J. Physiol. 254 (Endocrinol. Metab. 17): E459-E467, 1988.
5. Albina, J. E., C. D. Mills, W. L. Henry, and M. D. Caldwell. Temporal expression of different pathways of L-arginine metabolism in healing wounds. J. Immunol. 144:3877-3880, 1990.
6. Altschul, S. F., W. Gish, W. Miller, E. W. Myers, and D. J. Lipman. Basic local alignment search tool. J. Mol. Biol. 215: 403-410, 1990.
7. Barrandon, Y., and H. Green. Cell migration is essential for sustained growth of keratinocyte colonies: the roles of transforming growth factor-alpha and epidermal growth factor. Cell 50: 1131-1137, 1987.
8. Bernent, W. M., P. Forscher, and M. S. Mooseker. A novel cytoskeletal structure involved in purse string wound closure and cell polarity maintenance. J. Cell Biol. 121: 565-578, 1993.
9. Blay, J., and K. D. Brown. Epidermal growth factor promotes the chemotactic migration of cultured rat intestinal epithelial cells. J. Cell Physiol. 124: 107-112, 1985.
10. Bretcher, M. S. Endocytosis: relation to capping and cell locomotion. Science Wash. DC 224: 681-686, 1984.
11. Brundage, R. A., K. E. Fogarty, R. A. Tuft, and F. S. Fay. Chernotaxis of newt eosinophils: calcium regulation of the chemotactic response. Am. J. Phvsiol. 265 (Cell Physiol. 34): C1527-C1543, 1993.
12. Clancy, R. M., J. Leszczynska-Piziak, and S. B. Abramson. Nitric oxide stimulates the ADP-ribosylation of actin in human neutrophils. Biochem. Biophys Res. Commun. 191: 847-852, 1993.
13. Condeelis, J. Life at the leading edge: the formation of cell protrusions. Annu. Rev. Cell Biol. 9: 411-444, 1993.
14. Cornwell, T. L., E. Arnold, N. J. Boerth, and T. M. Lincoln. Inhibition of smooth muscle cell growth by nitric oxide and activation of cAMP-dependent protein kinase by cGMP. Am. J. Physiol. 267 (Cell Physiol. 36): C1405-C1413, 1994.
15. Gailit, J., D. Colflesh, I. Rabiner, J. Simone, and M. S. Goligorsky. Redistribution and dysfunction of integrins in cultured renal epithelial cells exposed to oxidative stress. Am J. Physiol. 264 (Renal Fluid Electrolyte Physiol. 33): F149-F157, 1993.
16. Garg, U. C., and A, Hassid. Nitric oxide-generating vasodilators and 8-bromo-cyclic guanosine monophosphate inhibit mitogenesis and proliferation of cultured rat vascular smooth muscle cells. J. Clin. Invest. 83: 1774-1777, 1989.
17. Gherardi, E., and M. Stocker. Hepatocyte growth factor-scatter factor: mitogen, motogen and Met. Cancer Cells 3: 227-232, 1991.
18. 3, DAG, and protein kinase C in newt eosinophils. J. Cell Biol. 127: 489-503, 1994.
19. 15N]nitrate in biological fluids. Anal. Biochem. 126: 131-138, 1982.
20. Hall, C. L., C. Wang, L. A. Lange, and E. A. Turley. Hyaluronan and the hyaluronan receptor RHAMM promote focal adhesion turnover and transient tyrosine kinase activity. J. Cell Biol. 126: 575-588, 1994.
21. Heck, D. E., D. L. Laskin, C. R. Gardner, and J. D. Laskin. Epidermal growth factor suppresses nitric oxide and hydrogen peroxide production by keratinocytes. Potential role for nitric oxide in the regulation of wound healing. J. Biol. Chem. 267: 21277-21280, 1992.
22. Henderson, S. A., P. H. Lee, E. E. Aeberhard, J. W. Adams, L. J. Ignarro, W. J. Murphy, and M. P. Sherman. Nitric oxide reduces early growth response-1 gene expression in rat lung macrophages treated with interferon-γ and lipopolysaccharide. J. Biol. Chem. 269: 25239-25242, 1994.
23. Hendey, B., C. B. Klee, and F. R. Maxfleld. Inhibition of neutrophil chemokinesis on vitronectin by inhibitors of calcineurin. Science Wash. DC 258: 296-299, 1992.
24. Hess, D. T., S. I. Patterson, D. N. Smith, and J. H. P. Skene. Neuronal growth cone collapse and inhibition of protein fatty acylation by nitnc oxide Nature Lond. 366: 562-565, 1993.
25. Ichimori, K., H. Ishida, M. Fukabori, H. Nakazawa, and E. Murakami. Practical nitric oxide measurement employing a nitric oxide-sensitive electrode. Rev. Sci. Instrum. 65: 1-5, 1994.
26. Kartha, S., and F. G. Toback. Adenine nucleotides stimulate migration in wounded cultures of kidney epithelial cells. J. Clin. Invest. 90: 288-292, 1992.
27. Ketteler, M., W. A. Border, and N. A. Noble. Cytokines and L-arginine in renal injury and repair. Am. J. Physiol. 267 (Renal Fluid Electrolyte Physiol. 36): F197-F207, 1994.
28. Kirk, S. J., M. Hurson, M. C. Regan, D. R. Holt, H. L. Wasserkrug, and A. Barbul. Arginine stimulates wound healing and immune function in elderly human beings. Surgery 114: 155-160, 1993
29. Leibovich, S. J., P. J. Polverini, T. W. Fong, L. A. Harlow, and A. E. Koch. Production of angiogenic activity by human monocytes requires an L-arginine/nitric oxide-synthase-dependent effector mechanism. Proc. Natl. Acad. Sci. USA 91: 4190-4194, 1994.
30. Marletta, M. A. Nitric oxide synthase: aspects concerning structure and catalysis. Cell 78: 927-930, 1994.
31. Marks, P. W., and F. R. Maxfield. Transient increases in cytosolic free calcium appear to be required for the migration of adherent human neutrophils. J. Cell Biol. 110: 43-52, 1990.
32. McCormack, S. A., J.-Y. Wang, M. J. Viar, L. Tague, P. J. A, Davies, and L. R. Johnson. Polyamines influence transglutaminase activity and cell migration in two cell lines. Am. J. Physiol. 267 (Cell Physiol. 36): C706-C714, 1994.
33. Mignatti, P., T. Morimoto, and D. B. Rifkin. Basic fibroblast growth factor released by single isolated cells stimulates their migration in an autocrine manner. Proc. Natl. Acad. Sci. USA 88: 11007-11011, 1991.
34. Nakao-Hayashi, J., H. Ito, T. Kanayasu, I. Morita, and S. Mirota. Stimulatory effects of insulin and insulin-like growth factor I on migration and tube formation by vascular endothelial cells. Atherosclerosis 92:141-149, 1992.
35. Nathan, C., and Q.-W. Xie. Nitric oxide synthases: roles, tolls, and controls. Cell 78: 915-918, 1994.
36. Nusrat, A., C. Delp, and J. L. Madara. Intestinal epithelial restitution: characterization of a cell culture model and mapping of cytoskeletal elements in migrating cells. J. Clin. Invest. 89: 1501-1511, 1992.
37. Obolenskaya, M., A. Schulzc-Specking, B. Plaumann, K. Frenzer, N. Freudenberg, and K, Decker. Nitric oxide production by cells isolated from regenerating rat liver. Biochem. Biophys. Res. Commun. 204: 1305-1311, 1994.
38. Pipili-Synetos, E., E. Sakkoula, and M. E. Maragoudakis. Nitric oxide is involved in the regulation of angiogenesis. Br. J. Pharmacol. 108: 855-857, 1993.
39. Reyes, A. A., B. H. Porras, F. I. Chasalow, and S. Klahr. L-Arginine decreases the infiltration of the kidney by macrophages in obstructive nephropathy and puromycin-induced nephrosis. Kidney Int. 45: 1346-1354, 1994.
40. Ruth, P., G. Wang, I. Boekhoff, B. May, A. Pfeifer, R. Penner, M. Korth, H. Breer, and F. Hofmann. Transfected cGMP-dependent protein kinase suppresses calcium transients by inhibition of inositol 1,4,5-trisphosphate production. Proc. Natl. Acad. Sci. USA 90: 2623-2627, 1993.
41. Schmidt, C. E., A. F. Horwitz, D. A. Lauffenburger, and M. P. Sheetz. Integrin-cytoskeletal interactions in migrating fibroblasts are dynamic, asymmetric, and regulated. J. Cell Biol. 123:977-991, 1993.
42. Seifert, E., G. Rettura, and S. M. Levenson. Arginine: an essential amino acid for injured rats. Surgery 84: 224-230, 1978.
43. Shibuki, K. An electrochemical microprobe for detecting nitric oxide release in brain tissue. Neurosci. Res. 9:69-76, 1990.
44. Shimonaka, M., and Y. Yamaguchi. Purification and biological characterization of epitaxin, a fibroblast-derived motility factor for epithelial cells. J. Biol. Chem. 269: 14284-14289, 1994.
45. Singer, S. J., and A. Kupfer. The directed migration of eukaryotic cells. Annu. Rev. Cell Biol. 2: 337-365, 1986
46. Stadnyk, A. W. Cytokine production by epithelial cells. FASEB J. 8: 1041-1047, 1994.
47. Stamler, J. S., D. J. Singel, and J. Loscalzo. Biochemistry of nitric oxide and its redox-activated forms. Science Wash. DC 258: 1898-1902, 1992.
48. Theriot, J. A., and T. J. Mitchison. Actin microfllament dynamics in locomoting cells. Nature Lond. 352: 126-131, 1991.
49. B receptor in endothelial cells. Receptor coupling to nitric oxide synthase. J. Biol. Chem. 269: 21778-21785, 1994.
50. Tsukahara, H., D, V. Gordienko, B. Tonshoff, M. C. Gelato, and M. S. Goligorsky. Direct demonstration of insulin-like growth factor-I-induced nitric oxide production by endothelial cells. Kidney Int. 45: 598-604, 1994.
51. Vincent, S. R., and H. Kimura. Histochemical mapping of nitric oxide synthase in the rat brain. Neuroscience 46: 755-784, 1992.
52. Zhang, G., T. Ichimura, A. Wallin, M. Kan, and J. L. Stevens. Regulation of rat proximal tubule epithelial cell growth by fibroblast growth factors, insulin-like growth factor-1 and transforming growth factor-β, and analysis of fibroblast growth factors in rat kidney. J. Cell. Physiol. 148:295-305, 1991.