Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1993 Aug;92(2):549–558. doi: 10.1172/JCI116622

Cytomegalovirus infection enhances smooth muscle cell proliferation and intimal thickening of rat aortic allografts.

K B Lemström 1, J H Bruning 1, C A Bruggeman 1, I T Lautenschlager 1, P J Häyry 1
PMCID: PMC294886  PMID: 8394384

Abstract

Inbred DA (AG-B4, RT1a) and WF (AG-B2, RT1v) rats were used as donors and recipients of aortic allografts. The recipient rats were inoculated i.p. either on day 1 (early infection) or on day 60 (late infection) with 10(5) plaque-forming units of rat cytomegalovirus (RCMV). The control rats were left noninfected. The presence of viral infection was demonstrated by plaque assays from biopsies of the salivary glands, liver, and spleen at sacrifice. The rats received 300 microCi[3H]thymidine by i.v. injection 3 h before sacrifice, and the grafts were removed at various time points for histology, immunohistochemistry, and autoradiography. RCMV infection significantly enhanced the generation of allograft arteriosclerosis. Infection at the time of transplantation had two important effects. First, the infection was associated with an early, prominent inflammatory episode and proliferation of inflammatory cells in the allograft adventitia. Second, the viral infection doubled the proliferation rate of smooth muscle cells and the arteriosclerotic alterations in the intima. In late infection the impact of RCMV infection on the allograft histology was nearly nonexistent. RCMV infection showed no effect in syngeneic grafts. These results suggest that early infection is more important to the generation of accelerated allograft arteriosclerosis than late infection, and that an acute alloimmune response must be associated with virus infection, to induce accelerated allograft arteriosclerosis. RCMV-infected aortic allografts, as described here, provide the first experimental model to investigate the interaction between the virus and the vascular wall of the transplant.

Full text

PDF
549

Images in this article

Selected References

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

  1. Barnhart G. R., Pascoe E. A., Mills A. S., Szentpetery S., Eich D. M., Mohanakumar T., Hastillo A., Thompson J. A., Hess M. L., Lower R. R. Accelerated coronary arteriosclerosis in cardiac transplant recipients. Transplant Rev (Orlando) 1987;1:31–46. doi: 10.1016/s0955-470x(87)80004-6. [DOI] [PubMed] [Google Scholar]
  2. Beck S., Barrell B. G. Human cytomegalovirus encodes a glycoprotein homologous to MHC class-I antigens. Nature. 1988 Jan 21;331(6153):269–272. doi: 10.1038/331269a0. [DOI] [PubMed] [Google Scholar]
  3. Benditt E. P., Barrett T., McDougall J. K. Viruses in the etiology of atherosclerosis. Proc Natl Acad Sci U S A. 1983 Oct;80(20):6386–6389. doi: 10.1073/pnas.80.20.6386. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Billingham M. E. Histopathology of graft coronary disease. J Heart Lung Transplant. 1992 May-Jun;11(3 Pt 2):S38–S44. [PubMed] [Google Scholar]
  5. Bruggeman C. A., Debie W. M., Grauls G., Majoor G., van Boven C. P. Infection of laboratory rats with a new cytomegalo-like virus. Arch Virol. 1983;76(3):189–199. doi: 10.1007/BF01311103. [DOI] [PubMed] [Google Scholar]
  6. Bruggeman C. A., Meijer H., Bosman F., van Boven C. P. Biology of rat cytomegalovirus infection. Intervirology. 1985;24(1):1–9. doi: 10.1159/000149612. [DOI] [PubMed] [Google Scholar]
  7. Bruggeman C. A., Meijer H., Dormans P. H., Debie W. M., Grauls G. E., van Boven C. P. Isolation of a cytomegalovirus-like agent from wild rats. Arch Virol. 1982;73(3-4):231–241. doi: 10.1007/BF01318077. [DOI] [PubMed] [Google Scholar]
  8. Bruning J. H., Debie W. H., Dormans P. H., Meijer H., Bruggeman C. A. The development and characterization of monoclonal antibodies against rat cytomegalovirus induced antigens. Arch Virol. 1987;94(1-2):55–70. doi: 10.1007/BF01313725. [DOI] [PubMed] [Google Scholar]
  9. Dummer J. S., White L. T., Ho M., Griffith B. P., Hardesty R. L., Bahnson H. T. Morbidity of cytomegalovirus infection in recipients of heart or heart-lung transplants who received cyclosporine. J Infect Dis. 1985 Dec;152(6):1182–1191. doi: 10.1093/infdis/152.6.1182. [DOI] [PubMed] [Google Scholar]
  10. Fabricant C. G., Fabricant J., Litrenta M. M., Minick C. R. Virus-induced atherosclerosis. J Exp Med. 1978 Jul 1;148(1):335–340. doi: 10.1084/jem.148.1.335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Friedman H. M., Macarak E. J., MacGregor R. R., Wolfe J., Kefalides N. A. Virus infection of endothelial cells. J Infect Dis. 1981 Feb;143(2):266–273. doi: 10.1093/infdis/143.2.266. [DOI] [PubMed] [Google Scholar]
  12. Fujinami R. S., Nelson J. A., Walker L., Oldstone M. B. Sequence homology and immunologic cross-reactivity of human cytomegalovirus with HLA-DR beta chain: a means for graft rejection and immunosuppression. J Virol. 1988 Jan;62(1):100–105. doi: 10.1128/jvi.62.1.100-105.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Gao S. Z., Alderman E. L., Schroeder J. S., Silverman J. F., Hunt S. A. Accelerated coronary vascular disease in the heart transplant patient: coronary arteriographic findings. J Am Coll Cardiol. 1988 Aug;12(2):334–340. doi: 10.1016/0735-1097(88)90402-0. [DOI] [PubMed] [Google Scholar]
  14. Grattan M. T., Moreno-Cabral C. E., Starnes V. A., Oyer P. E., Stinson E. B., Shumway N. E. Cytomegalovirus infection is associated with cardiac allograft rejection and atherosclerosis. JAMA. 1989 Jun 23;261(24):3561–3566. [PubMed] [Google Scholar]
  15. HAYFLICK L. THE LIMITED IN VITRO LIFETIME OF HUMAN DIPLOID CELL STRAINS. Exp Cell Res. 1965 Mar;37:614–636. doi: 10.1016/0014-4827(65)90211-9. [DOI] [PubMed] [Google Scholar]
  16. Hajjar D. P. Warner-Lambert/Parke-Davis Award Lecture. Viral pathogenesis of atherosclerosis. Impact of molecular mimicry and viral genes. Am J Pathol. 1991 Dec;139(6):1195–1211. [PMC free article] [PubMed] [Google Scholar]
  17. Hendrix M. G., Dormans P. H., Kitslaar P., Bosman F., Bruggeman C. A. The presence of cytomegalovirus nucleic acids in arterial walls of atherosclerotic and nonatherosclerotic patients. Am J Pathol. 1989 May;134(5):1151–1157. [PMC free article] [PubMed] [Google Scholar]
  18. Hendrix M. G., Salimans M. M., van Boven C. P., Bruggeman C. A. High prevalence of latently present cytomegalovirus in arterial walls of patients suffering from grade III atherosclerosis. Am J Pathol. 1990 Jan;136(1):23–28. [PMC free article] [PubMed] [Google Scholar]
  19. Hosenpud J. D., Shipley G. D., Wagner C. R. Cardiac allograft vasculopathy: current concepts, recent developments, and future directions. J Heart Lung Transplant. 1992 Jan-Feb;11(1 Pt 1):9–23. [PubMed] [Google Scholar]
  20. Hruban R. H., Wu T. C., Beschorner W. E., Cameron D. E., Ambinder R. F., Baumgartner W. A., Reitz B. A., Hutchins G. M. Cytomegalovirus nucleic acids in allografted hearts. Hum Pathol. 1990 Sep;21(9):981–982. doi: 10.1016/0046-8177(90)90186-9. [DOI] [PubMed] [Google Scholar]
  21. Iwamoto G. K., Monick M. M., Clark B. D., Auron P. E., Stinski M. F., Hunninghake G. W. Modulation of interleukin 1 beta gene expression by the immediate early genes of human cytomegalovirus. J Clin Invest. 1990 Jun;85(6):1853–1857. doi: 10.1172/JCI114645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Johnson D. E., Alderman E. L., Schroeder J. S., Gao S. Z., Hunt S., DeCampli W. M., Stinson E., Billingham M. Transplant coronary artery disease: histopathologic correlations with angiographic morphology. J Am Coll Cardiol. 1991 Feb;17(2):449–457. doi: 10.1016/s0735-1097(10)80114-7. [DOI] [PubMed] [Google Scholar]
  23. Keller R., Peitchel R., Goldman J. N., Goldman M. An IgG-Fc receptor induced in cytomegalovirus-infected human fibroblasts. J Immunol. 1976 Mar;116(3):772–777. [PubMed] [Google Scholar]
  24. Loebe M., Schüler S., Zais O., Warnecke H., Fleck E., Hetzer R. Role of cytomegalovirus infection in the development of coronary artery disease in the transplanted heart. J Heart Transplant. 1990 Nov-Dec;9(6):707–711. [PubMed] [Google Scholar]
  25. MacGregor R. R., Friedman H. M., Macarak E. J., Kefalides N. A. Virus infection of endothelial cells increases granulocyte adherence. J Clin Invest. 1980 Jun;65(6):1469–1477. doi: 10.1172/JCI109811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. McDonald K., Rector T. S., Braulin E. A., Kubo S. H., Olivari M. T. Association of coronary artery disease in cardiac transplant recipients with cytomegalovirus infection. Am J Cardiol. 1989 Aug 1;64(5):359–362. doi: 10.1016/0002-9149(89)90535-3. [DOI] [PubMed] [Google Scholar]
  27. Melnick J. L., Adam E., DeBakey M. E. Possible role of cytomegalovirus in atherogenesis. JAMA. 1990 Apr 25;263(16):2204–2207. [PubMed] [Google Scholar]
  28. Melnick J. L., Petrie B. L., Dreesman G. R., Burek J., McCollum C. H., DeBakey M. E. Cytomegalovirus antigen within human arterial smooth muscle cells. Lancet. 1983 Sep 17;2(8351):644–647. doi: 10.1016/s0140-6736(83)92529-1. [DOI] [PubMed] [Google Scholar]
  29. Mennander A., Tiisala S., Halttunen J., Yilmaz S., Paavonen T., Häyry P. Chronic rejection in rat aortic allografts. An experimental model for transplant arteriosclerosis. Arterioscler Thromb. 1991 May-Jun;11(3):671–680. doi: 10.1161/01.atv.11.3.671. [DOI] [PubMed] [Google Scholar]
  30. Reddehase M. J., Keil G. M., Koszinowski U. H. The cytolytic T lymphocyte response to the murine cytomegalovirus. I. Distinct maturation stages of cytolytic T lymphocytes constitute the cellular immune response during acute infection of mice with the murine cytomegalovirus. J Immunol. 1984 Jan;132(1):482–489. [PubMed] [Google Scholar]
  31. Reddehase M. J., Keil G. M., Koszinowski U. H. The cytolytic T lymphocyte response to the murine cytomegalovirus. II. Detection of virus replication stage-specific antigens by separate populations of in vivo active cytolytic T lymphocyte precursors. Eur J Immunol. 1984 Jan;14(1):56–61. doi: 10.1002/eji.1830140111. [DOI] [PubMed] [Google Scholar]
  32. Ross R. The pathogenesis of atherosclerosis--an update. N Engl J Med. 1986 Feb 20;314(8):488–500. doi: 10.1056/NEJM198602203140806. [DOI] [PubMed] [Google Scholar]
  33. Ross R., Wight T. N., Strandness E., Thiele B. Human atherosclerosis. I. Cell constitution and characteristics of advanced lesions of the superficial femoral artery. Am J Pathol. 1984 Jan;114(1):79–93. [PMC free article] [PubMed] [Google Scholar]
  34. Sharples L. D., Caine N., Mullins P., Scott J. P., Solis E., English T. A., Large S. R., Schofield P. M., Wallwork J. Risk factor analysis for the major hazards following heart transplantation--rejection, infection, and coronary occlusive disease. Transplantation. 1991 Aug;52(2):244–252. doi: 10.1097/00007890-199108000-00012. [DOI] [PubMed] [Google Scholar]
  35. Shellam G. R., Allan J. E., Papadimitriou J. M., Bancroft G. J. Increased susceptibility to cytomegalovirus infection in beige mutant mice. Proc Natl Acad Sci U S A. 1981 Aug;78(8):5104–5108. doi: 10.1073/pnas.78.8.5104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Smiley M. L., Mar E. C., Huang E. S. Cytomegalovirus infection and viral-induced transformation of human endothelial cells. J Med Virol. 1988 Jun;25(2):213–226. doi: 10.1002/jmv.1890250212. [DOI] [PubMed] [Google Scholar]
  37. Span A. H., Grauls G., Bosman F., van Boven C. P., Bruggeman C. A. Cytomegalovirus infection induces vascular injury in the rat. Atherosclerosis. 1992 Mar;93(1-2):41–52. doi: 10.1016/0021-9150(92)90198-p. [DOI] [PubMed] [Google Scholar]
  38. Stals F. S., Bosman F., van Boven C. P., Bruggeman C. A. An animal model for therapeutic intervention studies of CMV infection in the immunocompromised host. Arch Virol. 1990;114(1-2):91–107. doi: 10.1007/BF01311014. [DOI] [PubMed] [Google Scholar]
  39. The Registry of the International Society for Heart and Lung Transplantation: ninth official report--1992. J Heart Lung Transplant. 1992 Jul-Aug;11(4 Pt 1):599–606. [PubMed] [Google Scholar]
  40. Tumilowicz J. J., Gawlik M. E., Powell B. B., Trentin J. J. Replication of cytomegalovirus in human arterial smooth muscle cells. J Virol. 1985 Dec;56(3):839–845. doi: 10.1128/jvi.56.3.839-845.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Wentworth B. B., French L. Plaque assay of cytomegalovirus strains of human origin. Proc Soc Exp Biol Med. 1970 Nov;135(2):253–258. doi: 10.3181/00379727-135-35031. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES