| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Regular Articles |
From the Department of Surgery, Division of Surgical Research, Brown University and Rhode Island Hospital, Providence, Rhode Island
Tissue injury initiates a temporally ordered sequence of local cellular and metabolic responses presumably necessary for successful repair. Previous investigations demonstrated that metabolic evidence for nitric oxide synthase (NOS) activity is detectable in wounds only during the initial 48 to 72 hours of the repair process. Present results identify the cell types contributing inducible NOS (iNOS) to experimental wounds in rats. iNOS antigen was expressed in most macrophages present in wounds 6 to 24 hours after injury, and these cells exhibited NAPDH diaphorase and NOS activity. Polymorphonuclear leukocytes contained little iNOS antigen and no NADPH diaphorase activity and were minimally able to convert L-arginine to L-citrulline. The frequency of iNOS-positive macrophages declined on days 3 and 5 after wounding. By day 10, most macrophages in the wound were negative for iNOS. These cells, however, acquired iNOS antigen and activity in culture. Wound fluids, but not normal rat serum, suppressed the induction of iNOS during culture. Findings indicate that the expression of iNOS in healing wounds is restricted to macrophages present during the early phases of repair and that components of wound fluid suppress the induction of iNOS in macrophages in late wounds. Polymorphonuclear leukocytes contribute little iNOS activity to the healing wound.
This article has been cited by other articles:
![]() |
R. Torgler, S. E. Bongfen, J. C. Romero, A. Tardivel, M. Thome, and G. Corradin Sporozoite-Mediated Hepatocyte Wounding Limits Plasmodium Parasite Development via MyD88-Mediated NF-{kappa}B Activation and Inducible NO Synthase Expression J. Immunol., March 15, 2008; 180(6): 3990 - 3999. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Cetin, C. L. Leaphart, J. Li, I. Ischenko, M. Hayman, J. Upperman, R. Zamora, S. Watkins, H. R. Ford, J. Wang, et al. Nitric oxide inhibits enterocyte migration through activation of RhoA-GTPase in a SHP-2-dependent manner Am J Physiol Gastrointest Liver Physiol, May 1, 2007; 292(5): G1347 - G1358. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. A. Haroon, K. Amin, X. Jiang, and M. O. Arcasoy A Novel Role for Erythropoietin During Fibrin-Induced Wound-Healing Response Am. J. Pathol., September 1, 2003; 163(3): 993 - 1000. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Mahoney, J. Reichner, L. Robinson Bostom, B. Mastrofrancesco, W. Henry, and J. Albina Bacterial Colonization and the Expression of Inducible Nitric Oxide Synthase in Murine Wounds Am. J. Pathol., December 1, 2002; 161(6): 2143 - 2152. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. E. Albina, B. Mastrofrancesco, J. A. Vessella, C. A. Louis, W. L. Henry Jr., and J. S. Reichner HIF-1 expression in healing wounds: HIF-1alpha induction in primary inflammatory cells by TNF-alpha Am J Physiol Cell Physiol, December 1, 2001; 281(6): C1971 - C1977. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. P. Wang, X. Guo, M. W. L. Koo, B. C. Y. Wong, S. K. Lam, Y. N. Ye, and C. H. Cho Protective role of heme oxygenase-1 on trinitrobenzene sulfonic acid-induced colitis in rats Am J Physiol Gastrointest Liver Physiol, August 1, 2001; 281(2): G586 - G594. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Guhring, M. Gorig, M. Ates, O. Coste, H. U. Zeilhofer, A. Pahl, K. Rehse, and K. Brune Suppressed Injury-Induced Rise in Spinal Prostaglandin E2 Production and Reduced Early Thermal Hyperalgesia in iNOS-Deficient Mice J. Neurosci., September 1, 2000; 20(17): 6714 - 6720. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. J. Meszaros, J. S. Reichner, and J. E. Albina Macrophage-Induced Neutrophil Apoptosis J. Immunol., July 1, 2000; 165(1): 435 - 441. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. FRANK, B. STALLMEYER, H. KÄMPFER, N. KOLB, and J. PFEILSCHIFTER Nitric oxide triggers enhanced induction of vascular endothelial growth factor expression in cultured keratinocytes (HaCaT) and during cutaneous wound repair FASEB J, November 1, 1999; 13(14): 2002 - 2014. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |