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. 1974 Aug;71(8):3124–3128. doi: 10.1073/pnas.71.8.3124

Selective Thymic Localization of Murine Leukemia Virus-Related Antigens in C57BL/Ka Mice after Inoculation with Radiation Leukemia Virus

Alain Declève 1, Chikako Sato 1, Miriam Lieberman 1, Henry S Kaplan 1
PMCID: PMC388634  PMID: 4370358

Abstract

The tissue distribution and extent of virus-specific antigen expression were studied by immunofluorescence as a function of time and of lymphoma development in adult C57BL/Ka (Fv-1b) mice after intravenous injection of radiation leukemia virus, a B-tropic murine leukemia virus. Viral antigens were detected earlier in the thymus (1 week) than in the bone marrow, spleen, or lymph nodes (2-3 weeks). Despite an initial virus-induced thymic involution, the percentage of immunofluorescence-positive cells in the thymus rapidly increased thereafter to 65-80%, at which level it remained until 9 weeks, at which time increases in size and weight, histological changes, and an increased number of blastoid cells indicated the onset of lymphoma development in the thymus. In contrast, the percentage of immunofluorescence-positive cells in the bone marrow, spleen, and nodes remained low, and gradually decreased to zero within 8 weeks after thymectomy. The selective thymic localization of antigens induced by radiation leukemia virus in C57BL/Ka mice is in striking contrast to the previously reported ubiquitous tissue distribution of the Gross-AKR virus, an N-tropic virus, in its natural host, the Fv-1n, AKR strain with a high incidence of leukemia.

Keywords: immunofluorescence, thymus, bone marrow

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Selected References

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

  1. Boiron M., Lévy J. P., Périès J. In vitro investigations on murine leukemia viruses. Prog Med Virol. 1967;9:341–391. [PubMed] [Google Scholar]
  2. DOELL R. G., CARNES W. H. Urethan induction of thymic lymphoma in C57bl mice. Nature. 1962 May 12;194:588–589. doi: 10.1038/194588a0. [DOI] [PubMed] [Google Scholar]
  3. Decleve A., Gerber G. B., Leonard A., Lambiet-Collier M., Sassen A., Maisin J. R. Regneration of thymus, spleen and bone marrow in x-irradiated AKR mice. Radiat Res. 1972 Aug;51(2):318–332. [PubMed] [Google Scholar]
  4. Declève A., Niwa O., Hilgers J., Kaplan H. S. An improved murine leukemia virus immunofluorescence assay. Virology. 1974 Feb;57(2):491–502. doi: 10.1016/0042-6822(74)90188-3. [DOI] [PubMed] [Google Scholar]
  5. Duplan J. F. Recherches sur l'action leucémogène des extraits de tissus de souris C57BL. Bull Assoc Fr Etud Cancer. 1965 Apr-Jun;52(2):117–125. [PubMed] [Google Scholar]
  6. Haran-Ghera N. A leukemogenic filtrable agent from chemically-induced lymphoid leukemia in C57BL mice. Proc Soc Exp Biol Med. 1967 Mar;124(3):697–699. doi: 10.3181/00379727-124-31827. [DOI] [PubMed] [Google Scholar]
  7. Haran-Ghera N., Lieberman M., Kaplan H. S. Direct action of a leukemogenic virus on the thymus. Cancer Res. 1966 Mar;26(3):438–442. [PubMed] [Google Scholar]
  8. Haran-Ghera N. The mechanism of radiation action in leukemogenesis. 3. Thymolytic effect induced by the leukemogenic agent. Isr J Med Sci. 1968 Nov-Dec;4(6):1169–1180. [PubMed] [Google Scholar]
  9. Hilgers J., Nowinski R. C., Geering G., Hardy W. Detection of avian and mammalian oncogenic RNA viruses (oncornaviruses) by immunofluorescence. Cancer Res. 1972 Jan;32(1):98–106. [PubMed] [Google Scholar]
  10. Igel H. J., Huebner R. J., Turner H. C., Kotin P., Falk H. L. Mouse leukemia virus activation by chemical carcinogens. Science. 1969 Dec 26;166(3913):1624–1626. doi: 10.1126/science.166.3913.1624. [DOI] [PubMed] [Google Scholar]
  11. KAPLAN H. S. Influence of thymectomy, splenectomy, and gonadectomy on incidence of radiation-induced lymphoid tumors in strain C57 black mice. J Natl Cancer Inst. 1950 Aug;11(1):83–90. [PubMed] [Google Scholar]
  12. Kaplan H. S. On the natural history of the murine leukemias: presidential address. Cancer Res. 1967 Aug;27(8):1325–1340. [PubMed] [Google Scholar]
  13. LIEBERMAN M., HARAN-GHERA N., KAPLAN H. S. POTENTIATION OF VIRUS LEUKAEMOGENESIS IN C57BL MICE BY X-IRRADIATION OR URETHANE. Nature. 1964 Jul 25;203:420–422. doi: 10.1038/203420b0. [DOI] [PubMed] [Google Scholar]
  14. LIEBERMAN M., KAPLAN H. S. Leukemogenic activity of filtrates from radiation-induced lymphoid tumors of mice. Science. 1959 Aug 14;130(3372):387–388. doi: 10.1126/science.130.3372.387. [DOI] [PubMed] [Google Scholar]
  15. Lieberman M., Kaplan H. S. Lymphoid tumor induction by mouse thymocytes infected in vitro with radiation leukemia virus. Natl Cancer Inst Monogr. 1966 Sep;22:549–557. [PubMed] [Google Scholar]
  16. MILLER J. F. Analysis of the thymus influence in leukaemogenesis. Nature. 1961 Jul 15;191:248–249. doi: 10.1038/191248a0. [DOI] [PubMed] [Google Scholar]
  17. Metcalf D. Histologic and transplantation studies on preleukemic thymus of the AKR mouse. J Natl Cancer Inst. 1966 Oct;37(4):425–442. [PubMed] [Google Scholar]
  18. Micklem H. S., Ford C. E., Evans E. P., Gray J. Interrelationships of myeloid and lymphoid cells: studies with chromosome-marked cells transfused into lethally irradiated mice. Proc R Soc Lond B Biol Sci. 1966 Jul 19;165(998):78–102. doi: 10.1098/rspb.1966.0059. [DOI] [PubMed] [Google Scholar]
  19. Niwa O., Decléve A., Liberman M., Kaplan H. S. Adaptation of plaque assay methods to the in vitro quantitation of the radiation leukemia virus. J Virol. 1973 Jul;12(1):68–73. doi: 10.1128/jvi.12.1.68-73.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pincus T., Hartley J. W., Rowe W. P. A major genetic locus affecting resistance to infection with murine leukemia viruses. I. Tissue culture studies of naturally occurring viruses. J Exp Med. 1971 Jun 1;133(6):1219–1233. doi: 10.1084/jem.133.6.1219. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Pincus T., Rowe W. P., Lilly F. A major genetic locus affecting resistance to infection with murine leukemia viruses. II. Apparent identity to a major locus described for resistance to friend murine leukemia virus. J Exp Med. 1971 Jun 1;133(6):1234–1241. doi: 10.1084/jem.133.6.1234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. RUDALI G., SILBERMAN C. APPARITION DE LEUC'EMIES CHEZ DES SOURIS C57B1 APR'ES GREFFE D'ORGANES NORMAUX ISOLOGUES. Nouv Rev Fr Hematol. 1965 Jan-Feb;5:63–67. [PubMed] [Google Scholar]
  23. Rowe W. P., Pincus T. Quantitative studies of naturally occurring murine leukemia virus infection of AKR mice. J Exp Med. 1972 Feb 1;135(2):429–436. doi: 10.1084/jem.135.2.429. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. SIEGLER R., RICH M. A. UNILATERAL HISTOGENESIS OF AKR THYMIC LYMPHOMA. Cancer Res. 1963 Nov;23:1669–1678. [PubMed] [Google Scholar]

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