Brief hypoxia conditions monocytes to protect reperfused cardiocytes against cell death via the CD11b receptor

Journal of Heart and Lung Transplantation

Volumn 22, Issue 9, 2003, Pages 979-985

  DaCosta, Mark L ^a,d   Yao, Zhenhai ^b   MacPherson, Bradley C ^c   Jayakar, David V ^a   Jeevanandam, Valluvan ^a  

^a UNIVERSITY OF NORTH CAROLINA   (United States)

^b UNIVERSITY OF NORTH CAROLINA SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF CHICAGO   (United States)

^d NATIONAL UNIVERSITY HOSPITAL   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

BLOCKING ANTIBODY; CARBON DIOXIDE; CD11B ANTIGEN; IMMUNOGLOBULIN G; OXYGEN; PROPIDIUM IODIDE; RECEPTOR;

ARTICLE; CELL ADHESION; CELL CULTURE; CELL DEATH; CELL PROTECTION; CELL VIABILITY; CHICK EMBRYO; COCULTURE; CONTROLLED STUDY; EMBRYO; EXPERIMENTAL TEST; FLOW CYTOMETRY; FLOW RATE; HUMAN; HUMAN CELL; HYPOXIA; MONOCYTE; MUSCLE CELL; PH; PRIORITY JOURNAL; PROTEIN EXPRESSION; REOXYGENATION; REPERFUSION; STATISTICAL SIGNIFICANCE; TISSUE FIXATION;

EID: 0042236725     PISSN: 10532498     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1053-2498(02)01161-0     Document Type: Article

References (36)

1. Downey J.M. Ischemic preconditioning nature's own cardioprotective intervention . Trends Cardiovasc Med. 2:1992;170-176.
2. Yao Z., Gross G.J. Acetylcholine mimics ischemic preconditioning via a glibenclamide-sensitive mechanism in dogs. Am J Physiol. 264:1993;H2221-2225.
3. ATP channels. Am J Physiol Heart Circ Physiol. 279:(4):2000;1858-1863.
4. ATP channels in myocytes. Circulation. 103:2001;290-295.
5. Murry C.E., Jennings R.B., Reimer K.A. Preconditioning with ischemia a delay of lethal cell injury in ischemic myocardium . Circulation. 74:1986;1124-1136.
6. Entman M.L., Rossen M.L., Dreyer W.J., Anderson D.C., Taylor A.A., Smith C.W. Inflammation in the course of early myocardial ischemia. FASEB J. 5:1991;2529-2537.
7. Kamikubo Y., Murakami M., Imamura M., Murashita T., Yasuda K., Uede T. Neutrophil-independent myocardial dysfunction during an early stage of global ischemia and reperfusion of isolated hearts. Immunopharmacology. 29:1995;261-271.
8. Birdsall H.H., Green D.M., Trial J., et al. Complement C5a, TGF-beta 1 and MCP-1 in sequence induce the migration of monocytes into ischemic canine myocardium within the first one to five hours after reperfusion. Circulation. 95:1997;684-692.
9. Entman M.L., Youker K., Shoji T., et al. Neutrophil induced oxidative injury of cardiac myocytes A compartmented system requiring CD11b/CD18-ICAM-1 adherence . J Clin Invest. 90:1992;1335-1345.
10. Hansen P.R., Stawski G. Neutrophil mediated damage to isolated myocytes after anoxia and reoxygenation. Cardiovasc Res. 28:1994;565-569.
11. Lucchesi B.R., Werns S.W., Fantone J.C. The role of neutrophil and free radicals in ischemic myocardial injury. J Mol Cell Cardiol. 21:1989;1241-1251.
12. Hill J.H., Ward P.A. The phlogistic role of C3 leukotactic fragments in myocardial infarcts in rats. J Exp Med. 133:1970;885-900.
13. Toyozaki T., Saito T., Takano H., et al. Expression of intercellular adhesion molecule-1 on cardiac myocytes for myocarditis before and during immunosuppressive therapy. Am J Cardiol. 72:1995;441-444.
14. Yamamoto A., Wenthold R.J. Jr, Zhang J., Herman E.H., Ferrans V.J. Immunofluorescence techniques for the identification of immune effector cells in rat heart applications to the study of the myocarditis induced by interleukin-2 . J Mol Cell Cardiol. 27:1995;307-319.
15. Finkel M.S., Oddis C.V., Jacob T.D., Watkins S.C., Hattler B.G., Simmons R.L. Negative inotropic effects of cytokines on the heart mediated by nitric oxide. Science. 257:1992;387-389.
16. Xie Y.W., Wolin M.S. Role of nitric oxide and its interaction with superoxide in the suppression of cardiac muscle mitochondrial respiration Involvement in response to hypoxia-reoxygenation . Circulation. 94:1996;2580-2586.
17. Landay A., Gartland L., Clement L.T. Characterization of a phenotypically distinct subpopulation of Leu-2+ cells which suppress T cell proliferative responses. J Immunol. 131:1983;2757.
18. Schulz R.D., Panas D.L., Catena R., Moncada S., Olley P.M., Lopaschuk G.D. The role of nitric oxide in cardiac depression induced by interleukin-1beta and tumor necrosis factor-alpha. Br J Pharmacol. 114:1995;27-34.
19. Brady A.J., Poole-Wilson P.A., Harding S.E., Warren J.B. Nitric oxide production within cardiac myocytes reduces their contractility in endotoxemia. Am J Physiol Heart Circ Physiol. 263:1992;H1963-1966.
20. Simms M.G., Walley K.R. Activated macrophages decrease rat cardiac myocyte contractility importance of ICAM-1-dependant adhesion . Am J Physiol. 277:(1):1999;253-260.
21. Aziz S., McDonald T.O., Gohra H. Transplant arterial vasculopathy evidence for a dual pattern of endothelial injury and the source of smooth muscle cells in lesions of intimal hyperplasia . J Heart Lung Transplant. 14:1995;S123-136.
22. Wasowska B.A., Zheng X.X., Strom T.B., Kupieck-Weglinski J.W. Adjunctive rapamycin and CsA treatment inhibits monocyte/macrophage associated cytokines/chemokines in sensitized cardiac graft recipients. Transplantation. 71:(8):2001;1179-1183.
23. Xu B., Sakkas L.I., Slachta C.A., et al. Apoptosis in chronic rejection of human cardiac allografts. Transplantation. 71:(8):2001;1137-1146.
24. Fyfe A.I., Stevenson L.W., Harper C.M., et al. Recipient mononuclear cell recognition and adhesion to graft endothelium after human cardiac transplantation Lymphocyte recognition leads to monocyte adhesion . J Clin Invest. 94:(5):1994;2142-2147.
25. Deng M.C., Erren M., Roeder N., et al. T-cell and monocyte subsets, inflammatory molecules, rejection, and hemodynamics early after cardiac transplantation. Transplantation. 65:(9):1998;1255-1261.
26. Yamashita N., Hoshida S., Otsu K., Taniguchi N., Kuzuya T., Hori M. The involvement of cytokines in the second window of ischaemic preconditioning. Br J Pharmacol. 131:2000;415-422.
27. Liu H., McPherson B.C., Zhu X., Da Costa M.L.A., Jeevanandam V., Yao Z. Role of nitric oxide and protein kinase C in acetylcholine-induced cardioprotection. Am J Physiol. 281:2001;H191-197.
28. Barry W.H., Pober J., Marsh J.D., Frankel S.R., Smith T.W. Effects of graded hypoxia on contraction of cultured chick embryo ventricular cells. Am J Physiol. 239:1980;H651-657.
29. Vanden Hoek T.L., Shao Z., Li C., Zak R., Schumacker P.T., Becker L.B. Reperfusion injury on cardiac cardiomyocytes after simulated ischemia. Am J Physiol. 270:1996;H1334-1341.
30. Lo L.W., Koch C.J., Wilson D.F. Calibration of oxygen-dependent quenching of the phosphorescence of Pd-meso-tetra (4-carboxyphenyl) porphine a phosphor with general application for measuring oxygen concentration in biological systems . Anal Biochem. 236:1996;153-160.
31. Wilson D.F., Rumsey W.L., Green T.J., Vanderkooi J.M. The oxygen dependence of mitochondrial oxidative phosphorylation measured by a new optical method for measuring oxygen concentration. J Biol Chem. 263:1988;2712-2718.
32. Chandel N.S., Budinger G.R.S., Schumacker P.T. Molecular oxygen modulates cytochrome c oxidase function. J Biol Chem. 271:1996;18672-18677.
33. Yao Z., Tong J., Tan X., et al. Role of reactive oxygen species in acetylcholine-induced preconditioning in cardiomyocytes. Am J Physiol. 277:1999;H2504-2509.
34. Vanden Hoek T.L., Becker L.B., Shao Z., Li C., Schumacker P.T. Reactive oxygen species released from mitochondria during brief hypoxia induce preconditioning in cardiomyocytes. J Biol Chem. 273:1998;18092-18098.
35. Bond J.M., Herman B., Lemasters J.J. Recovery of cultured rat neonatal cardiomyocytes from hypercontracture after chemical hypoxia. Res Commun Chem Pathol Pharmacol. 71:1991;195-208.
36. Ambrosio G.A., Tritto I., Chiariello M. The role of oxygen free radicals in preconditioning. J Mol Cell Cardiol. 27:1995;1035-1039.