Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1962 Oct 1;116(4):407–422. doi: 10.1084/jem.116.4.407

INTRACELLULAR LOCALIZATION AND QUANTITATION OF TRITIATED ANTIGENS IN RETICULOENDOTHELIAL TISSUES OF MICE DURING SECONDARY AND HYPERIMMUNE RESPONSES

Audrey N Roberts 1, Felix Haurowitz 1
PMCID: PMC2137631  PMID: 13974279

Abstract

Autoradiography and quantitative radiochemical techniques have been used to determine intracellular localization of tritium and the quantity of tissue-bound tritium, respectively, following injections of H3-aniline azo PGG or H3-arsanilazo PGG to yield hyperimmune or secondary response stimulation in mice. Autoradiography revealed intracytoplasmic localization of grains in macrophages of spleen and lung sections, and in Kupffer cells of liver sections following intravenous and subcutaneous injections of H3-aniline azo PGG. Quantitation of tissue section surface radioactivities in the windowless flow counter and scintillation counter, and of dissolved tissue section activities in the scintillation counter, showed that greatest radioactivity was present in lung tissue, with less in spleen, liver, and mesenteric lymph nodes from these hyperimmunized mice. Autoradiographic studies on tissue sections from mice in secondary response stimulation after subcutaneous foot-pad injections of H3-arsanilazo PGG, showed intracellular and extracellular grains over regional popliteal node sections, with intracytoplasmic grain localization over macrophages and pyroninophilic plasmacytes. Scattered macrophages in spleen and lung sections also contained intracytoplasmic radioactivity. Clusters of antibody-synthesizing cells in the regional lymph nodes were demonstrated with fluorescence microscopy, and these cells were compared to similar cells possessing radioactivity as observed in the section autoradiographs. An occasional Russell body plasma cell containing specific antibody was observed in splenic impressions. Windowless flow counting showed that greatest radioactivity was in regional node sections, with less in spleen and lung, and none in contralateral lymph nodes. A quantitative comparison between windowless flow counting and autoradiography revealed that 20 counts were required to yield one silver grain.

Full Text

The Full Text of this article is available as a PDF (1.3 MB).

Selected References

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

  1. BOYDEN S. V. The adsorption of proteins on erythrocytes treated with tannic acid and subsequent hemagglutination by antiprotein sera. J Exp Med. 1951 Feb;93(2):107–120. doi: 10.1084/jem.93.2.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. CHENG H. F., DICKS M., SHELLHAMER R. H., BROWN E. S., ROBERTS A. N., HAUROWITZ F. Localization of antigens by autoradiography. Proc Soc Exp Biol Med. 1961 Jan;106:93–97. doi: 10.3181/00379727-106-26248. [DOI] [PubMed] [Google Scholar]
  3. COONS A. H., LEDUC E. H., CONNOLLY J. M. Studies on antibody production. I. A method for the histochemical demonstration of specific antibody and its application to a study of the hyperimmune rabbit. J Exp Med. 1955 Jul 1;102(1):49–60. doi: 10.1084/jem.102.1.49. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. COONS A. H., LEDUC E. H., KAPLAN M. H. Localization of antigen in tissue cells. VI. The fate of injected foreign proteins in the mouse. J Exp Med. 1951 Feb;93(2):173–188. doi: 10.1084/jem.93.2.173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. CRAMPTON C. F., RELLER H. H., HAUROWITZ F. Deposition of beef serum gamma-globulin in rabbit organs and subcellular fractions. J Immunol. 1953 Nov;71(5):319–324. [PubMed] [Google Scholar]
  6. CRAMPTON C. F., RELLER H. H., HAUROWITZ F. Persistence of C14 anthranil-azo-ovalbumin in injected rabbits. Proc Soc Exp Biol Med. 1952 Jul;80(3):448–451. doi: 10.3181/00379727-80-19653. [DOI] [PubMed] [Google Scholar]
  7. DIXON F. J., WEIGLE W. O., ROBERTS J. C. Comparison of antibody responses associated with the transfer of rabbit lymph-node, peritoneal exudate, and thymus cells. J Immunol. 1957 Jan;78(1):56–62. [PubMed] [Google Scholar]
  8. FISHMAN M. Antibody formation in vitro. J Exp Med. 1961 Dec 1;114:837–856. doi: 10.1084/jem.114.6.837. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GARVEY J. S., CAMPBELL D. H. Studies of the retention and properties of S35 labeled antigen in livers of immunized rabbits. J Immunol. 1956 Jan;76(1):36–45. [PubMed] [Google Scholar]
  10. GARVEY J. S., CAMPBELL D. H. The in vivo identification in liver tissue of an S35 azo label with its protein carrier. Arch Biochem Biophys. 1958 Feb;73(2):507–508. doi: 10.1016/0003-9861(58)90294-7. [DOI] [PubMed] [Google Scholar]
  11. GARVEY J. S., CAMPBELL D. H. The retention of S35-labelled bovine serum albumin in normal and immunized rabbit liver tissue. J Exp Med. 1957 Apr 1;105(4):361–372. doi: 10.1084/jem.105.4.361. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. GAVOSTO F., FICQ A. Radioautographic study of the localization of tobacco mosaic virus antigen. Nature. 1953 Aug 29;172(4374):406–407. doi: 10.1038/172406a0. [DOI] [PubMed] [Google Scholar]
  13. GITLIN D., LANDING B. H., WHIPPLE A. Composition of mitochondrial preparations in relation to intracellular localization of azoprotein in the mouse. Proc Soc Exp Biol Med. 1951 Nov;78(2):631–635. doi: 10.3181/00379727-78-19164. [DOI] [PubMed] [Google Scholar]
  14. HAUROWITZ F., CRAMPTON C. F. The fate in rabbits of intravenously injected I131-iodoovalbumin. J Immunol. 1952 Jan;68(1):73–85. [PubMed] [Google Scholar]
  15. HAUROWITZ F. Use of radioisotopes in immunochemical research. Ergeb Mikrobiol Immunitatsforsch Exp Ther. 1961;34:1–26. doi: 10.1007/978-3-662-38352-0_1. [DOI] [PubMed] [Google Scholar]
  16. HAWKINS J. D., HAUROWITZ F. The recovery of injected antigens from rat spleens. Biochem J. 1961 Jul;80:200–210. doi: 10.1042/bj0800200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. KRUSE H., McMASTER P. D. The distribution and storage of blue antigenic azoproteins in the tissues of mice. J Exp Med. 1949 Nov;90(5):425–446. doi: 10.1084/jem.90.5.425. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  19. MARSHALL J. D., EVELAND W. C., SMITH C. W. Superiority of fluorescein isothiocyanate (Riggs) for fluorescent-antibody technic with a modification of its application. Proc Soc Exp Biol Med. 1958 Aug-Sep;98(4):898–900. doi: 10.3181/00379727-98-24222. [DOI] [PubMed] [Google Scholar]
  20. RIGGS J. L., SEIWALD R. J., BURCKHALTER J. H., DOWNS C. M., METCALF T. G. Isothiocyanate compounds as fluorescent labeling agents for immune serum. Am J Pathol. 1958 Nov-Dec;34(6):1081–1097. [PMC free article] [PubMed] [Google Scholar]
  21. ROBERTS J. C., Jr, DIXON F. J., WEIGLE W. O. Antibody-producing lymph node cells and peritoneal exudate cells; morphologic studies of transfers to immunologically inert rabbits. AMA Arch Pathol. 1957 Sep;64(3):324–332. [PubMed] [Google Scholar]
  22. ROBERTSON J. S., BOND V. P., CRONKITE E. P. Resolution and image spread in autoradiographs of tritium-labeled cells. Int J Appl Radiat Isot. 1959 Nov;7:33–37. doi: 10.1016/0020-708x(59)90277-7. [DOI] [PubMed] [Google Scholar]
  23. ROBERTSON J. S. The response of the macrophage to antigenic azoprotein, studies in the rabbit ear chamber preparation. Aust J Exp Biol Med Sci. 1952 Feb;30(1):59–71. doi: 10.1038/icb.1952.6. [DOI] [PubMed] [Google Scholar]
  24. STAVITSKY A. B. Micromethods for the study of proteins and antibodies. I. Procedure and general applications of hemagglutination and hemagglutination-inhibition reactions with tannic acid and protein-treated red blood cells. J Immunol. 1954 May;72(5):360–367. [PubMed] [Google Scholar]
  25. Sabin F. R. CELLULAR REACTIONS TO A DYE-PROTEIN WITH A CONCEPT OF THE MECHANISM OF ANTIBODY FORMATION. J Exp Med. 1939 Jun 30;70(1):67–82. doi: 10.1084/jem.70.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Smetana H., Johnson F. R. The Origin of Colloid and Lipoid Droplets in the Epithelial Cells of the Renal Tubules. Am J Pathol. 1942 Nov;18(6):1029–1049. [PMC free article] [PubMed] [Google Scholar]
  27. TERRES G., WOLINS W. Immune degradation in passively sensitized mice. I. Degradation of antigen as a function of the amount of antigen and antibody used. J Immunol. 1959 Jul;83(1):9–16. [PubMed] [Google Scholar]

Articles from The Journal of Experimental Medicine are provided here courtesy of The Rockefeller University Press

RESOURCES