Skip to main content
The American Journal of Pathology logoLink to The American Journal of Pathology
. 1997 Aug;151(2):531–538.

Macrophage apoptosis in rat crescentic glomerulonephritis.

H Y Lan 1, H Mitsuhashi 1, Y Y Ng 1, D J Nikolic-Paterson 1, N Yang 1, W Mu 1, R C Atkins 1
PMCID: PMC1858016  PMID: 9250165

Abstract

The fate of macrophages at the site of inflammation is unknown. We investigated this question in a macrophage-mediated model of crescentic glomerulonephritis in which macrophage accumulation is relatively stable despite the presence of high levels of local macrophage proliferation. Accelerated anti-glomerular basement membrane glomerulonephritis was induced in groups of six rats that were killed on day 1, 7, 14, or 21. Macrophage apoptosis was demonstrated in kidney sections by three methods: in situ terminal deoxyribonucleotide transferase (TdT)-mediated dUTP nick end labeling (TUNEL) combined with ED1 antibody immunostaining of macrophages, ED1 immunostaining combined with classical nuclear morphology, and electron microscopy. Substantial macrophage apoptosis became evident on day 14 of the disease, following the appearance of high levels of macrophage proliferation. The parallel relationship between proliferation and apoptosis is the likely explanation for the stabilization of macrophage numbers within the inflamed kidney. A striking feature was that macrophage proliferation and apoptosis was largely restricted to areas of focal damage, such as in the development of glomerular crescents. Increasing levels of macrophage proliferation and apoptosis were evident as crescents developed from a cellular to a fibrocellular phenotype, with a dramatic reduction in both of these processes in the progression to a fibrotic phenotype, suggesting an important role for macrophage apoptosis in the resolution of fibrocellular crescents to an acellular fibrotic structure. In conclusion, this study has identified apoptosis as an important mechanism counterbalancing local proliferation in the regulation of macrophage accumulation at sites of inflammation. Indeed, apoptosis may be a central regulator of the progression and resolution of macrophage-mediated tissue injury.

Full text

PDF
531

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Atkins R. C., Nikolic-Paterson D. J., Song Q., Lan H. Y. Modulators of crescentic glomerulonephritis. J Am Soc Nephrol. 1996 Nov;7(11):2271–2278. doi: 10.1681/ASN.V7112271. [DOI] [PubMed] [Google Scholar]
  2. Baker A. J., Mooney A., Hughes J., Lombardi D., Johnson R. J., Savill J. Mesangial cell apoptosis: the major mechanism for resolution of glomerular hypercellularity in experimental mesangial proliferative nephritis. J Clin Invest. 1994 Nov;94(5):2105–2116. doi: 10.1172/JCI117565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Bellingan G. J., Caldwell H., Howie S. E., Dransfield I., Haslett C. In vivo fate of the inflammatory macrophage during the resolution of inflammation: inflammatory macrophages do not die locally, but emigrate to the draining lymph nodes. J Immunol. 1996 Sep 15;157(6):2577–2585. [PubMed] [Google Scholar]
  4. Cleveland J. L., Ihle J. N. Contenders in FasL/TNF death signaling. Cell. 1995 May 19;81(4):479–482. doi: 10.1016/0092-8674(95)90068-3. [DOI] [PubMed] [Google Scholar]
  5. Damoiseaux J. G., Döpp E. A., Calame W., Chao D., MacPherson G. G., Dijkstra C. D. Rat macrophage lysosomal membrane antigen recognized by monoclonal antibody ED1. Immunology. 1994 Sep;83(1):140–147. [PMC free article] [PubMed] [Google Scholar]
  6. Desmoulière A., Redard M., Darby I., Gabbiani G. Apoptosis mediates the decrease in cellularity during the transition between granulation tissue and scar. Am J Pathol. 1995 Jan;146(1):56–66. [PMC free article] [PubMed] [Google Scholar]
  7. Dijkstra C. D., Döpp E. A., Joling P., Kraal G. The heterogeneity of mononuclear phagocytes in lymphoid organs: distinct macrophage subpopulations in the rat recognized by monoclonal antibodies ED1, ED2 and ED3. Immunology. 1985 Mar;54(3):589–599. [PMC free article] [PubMed] [Google Scholar]
  8. Gavrieli Y., Sherman Y., Ben-Sasson S. A. Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation. J Cell Biol. 1992 Nov;119(3):493–501. doi: 10.1083/jcb.119.3.493. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Goto M., Matsuno K., Yamaguchi Y., Ezaki T., Ogawa M. Proliferation kinetics of macrophage subpopulations in a rat experimental pancreatitis model. Arch Histol Cytol. 1993 Mar;56(1):75–82. doi: 10.1679/aohc.56.75. [DOI] [PubMed] [Google Scholar]
  10. Grigg J. M., Savill J. S., Sarraf C., Haslett C., Silverman M. Neutrophil apoptosis and clearance from neonatal lungs. Lancet. 1991 Sep 21;338(8769):720–722. doi: 10.1016/0140-6736(91)91443-x. [DOI] [PubMed] [Google Scholar]
  11. Holzman L. B., Wiggins R. C. Consequences of glomerular injury. Glomerular crescent formation. Semin Nephrol. 1991 May;11(3):346–353. [PubMed] [Google Scholar]
  12. Hruby Z. W., Shirota K., Jothy S., Lowry R. P. Antiserum against tumor necrosis factor-alpha and a protease inhibitor reduce immune glomerular injury. Kidney Int. 1991 Jul;40(1):43–51. doi: 10.1038/ki.1991.177. [DOI] [PubMed] [Google Scholar]
  13. Hughes J., Johnson R. J., Mooney A., Hugo C., Gordon K., Savill J. Neutrophil fate in experimental glomerular capillary injury in the rat. Emigration exceeds in situ clearance by apoptosis. Am J Pathol. 1997 Jan;150(1):223–234. [PMC free article] [PubMed] [Google Scholar]
  14. Kerr P. G., Nikolic-Paterson D. J., Lan H. Y., Tesch G., Rainone S., Atkins R. C. Deoxyspergualin suppresses local macrophage proliferation in rat renal allograft rejection. Transplantation. 1994 Sep 15;58(5):596–601. doi: 10.1097/00007890-199409150-00012. [DOI] [PubMed] [Google Scholar]
  15. Lan H. Y., Mu W., Nikolic-Paterson D. J., Atkins R. C. A novel, simple, reliable, and sensitive method for multiple immunoenzyme staining: use of microwave oven heating to block antibody crossreactivity and retrieve antigens. J Histochem Cytochem. 1995 Jan;43(1):97–102. doi: 10.1177/43.1.7822770. [DOI] [PubMed] [Google Scholar]
  16. Lan H. Y., Nikolic-Paterson D. J., Atkins R. C. Trafficking of inflammatory macrophages from the kidney to draining lymph nodes during experimental glomerulonephritis. Clin Exp Immunol. 1993 May;92(2):336–341. doi: 10.1111/j.1365-2249.1993.tb03401.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lan H. Y., Nikolic-Paterson D. J., Mu W., Atkins R. C. Local macrophage proliferation in the progression of glomerular and tubulointerstitial injury in rat anti-GBM glomerulonephritis. Kidney Int. 1995 Sep;48(3):753–760. doi: 10.1038/ki.1995.347. [DOI] [PubMed] [Google Scholar]
  18. Lan H. Y., Nikolic-Paterson D. J., Mu W., Vannice J. L., Atkins R. C. Interleukin-1 receptor antagonist halts the progression of established crescentic glomerulonephritis in the rat. Kidney Int. 1995 May;47(5):1303–1309. doi: 10.1038/ki.1995.185. [DOI] [PubMed] [Google Scholar]
  19. Lan H. Y., Paterson D. J., Atkins R. C. Initiation and evolution of interstitial leukocytic infiltration in experimental glomerulonephritis. Kidney Int. 1991 Sep;40(3):425–433. doi: 10.1038/ki.1991.229. [DOI] [PubMed] [Google Scholar]
  20. Lan H. Y., Yang N., Metz C., Mu W., Song Q., Nikolic-Paterson D. J., Bacher M., Bucala R., Atkins R. C. TNF-alpha up-regulates renal MIF expression in rat crescentic glomerulonephritis. Mol Med. 1997 Feb;3(2):136–144. [PMC free article] [PubMed] [Google Scholar]
  21. Morel-Maroger Striker L., Killen P. D., Chi E., Striker G. E. The composition of glomerulosclerosis. I. Studies in focal sclerosis, crescentic glomerulonephritis, and membranoproliferative glomerulonephritis. Lab Invest. 1984 Aug;51(2):181–192. [PubMed] [Google Scholar]
  22. Noronha I. L., Krüger C., Andrassy K., Ritz E., Waldherr R. In situ production of TNF-alpha, IL-1 beta and IL-2R in ANCA-positive glomerulonephritis. Kidney Int. 1993 Mar;43(3):682–692. doi: 10.1038/ki.1993.98. [DOI] [PubMed] [Google Scholar]
  23. Savill J. S., Wyllie A. H., Henson J. E., Walport M. J., Henson P. M., Haslett C. Macrophage phagocytosis of aging neutrophils in inflammation. Programmed cell death in the neutrophil leads to its recognition by macrophages. J Clin Invest. 1989 Mar;83(3):865–875. doi: 10.1172/JCI113970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Schmied M., Breitschopf H., Gold R., Zischler H., Rothe G., Wekerle H., Lassmann H. Apoptosis of T lymphocytes in experimental autoimmune encephalomyelitis. Evidence for programmed cell death as a mechanism to control inflammation in the brain. Am J Pathol. 1993 Aug;143(2):446–452. [PMC free article] [PubMed] [Google Scholar]
  25. Shimizu A., Kitamura H., Masuda Y., Ishizaki M., Sugisaki Y., Yamanaka N. Apoptosis in the repair process of experimental proliferative glomerulonephritis. Kidney Int. 1995 Jan;47(1):114–121. doi: 10.1038/ki.1995.13. [DOI] [PubMed] [Google Scholar]
  26. Shimizu A., Masuda Y., Kitamura H., Ishizaki M., Sugisaki Y., Yamanaka N. Apoptosis in progressive crescentic glomerulonephritis. Lab Invest. 1996 May;74(5):941–951. [PubMed] [Google Scholar]
  27. Silva F. G., Hoyer J. R., Pirani C. L. Sequential studies of glomerular crescent formation in rats with antiglomerular basement membrane-induced glomerulonephritis and the role of coagulation factors. Lab Invest. 1984 Oct;51(4):404–415. [PubMed] [Google Scholar]
  28. Thepen T., Claassen E., Hoeben K., Brevé J., Kraal G. Migration of alveolar macrophages from alveolar space to paracortical T cell area of the draining lymph node. Adv Exp Med Biol. 1993;329:305–310. doi: 10.1007/978-1-4615-2930-9_51. [DOI] [PubMed] [Google Scholar]
  29. Thompson C. B. Apoptosis in the pathogenesis and treatment of disease. Science. 1995 Mar 10;267(5203):1456–1462. doi: 10.1126/science.7878464. [DOI] [PubMed] [Google Scholar]
  30. Tipping P. G., Leong T. W., Holdsworth S. R. Tumor necrosis factor production by glomerular macrophages in anti-glomerular basement membrane glomerulonephritis in rabbits. Lab Invest. 1991 Sep;65(3):272–279. [PubMed] [Google Scholar]
  31. Waseem N. H., Lane D. P. Monoclonal antibody analysis of the proliferating cell nuclear antigen (PCNA). Structural conservation and the detection of a nucleolar form. J Cell Sci. 1990 May;96(Pt 1):121–129. doi: 10.1242/jcs.96.1.121. [DOI] [PubMed] [Google Scholar]
  32. Yoshioka K., Takemura T., Murakami K., Okada M., Yagi K., Miyazato H., Matsushima K., Maki S. In situ expression of cytokines in IgA nephritis. Kidney Int. 1993 Oct;44(4):825–833. doi: 10.1038/ki.1993.317. [DOI] [PubMed] [Google Scholar]
  33. van Furth R. Origin and turnover of monocytes and macrophages. Curr Top Pathol. 1989;79:125–150. [PubMed] [Google Scholar]

Articles from The American Journal of Pathology are provided here courtesy of American Society for Investigative Pathology

RESOURCES