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. 1951 Jan 31;93(2):173–188. doi: 10.1084/jem.93.2.173

LOCALIZATION OF ANTIGEN IN TISSUE CELLS

VI. THE FATE OF INJECTED FOREIGN PROTEINS IN THE MOUSE

Albert H Coons 1, Elizabeth H Leduc 1, Melvin H Kaplan 1; With the Technical Assistance of Jeanne M. Connolly1
PMCID: PMC2136059  PMID: 14803641

Abstract

The fate of three proteins, crystalline hen's egg albumin, crystalline bovine plasma albumin, and human plasma γ-globulin, was traced after intravenous injection into mice. This was done by preparing frozen sections of quick-frozen tissue, allowing what foreign protein might be present in the section to react with homologous antibody labelled with fluorescein, and examining the section under the fluorescence microscope. By this means, which employs the serological specificity of the protein as a natural "marker," all three of these proteins were found in the cells of the reticulo-endothelial system, the connective tissue, the vascular endothelium, the lymphocytes of spleen and lymph node, and the epithelium of the kidney tubules, the liver, and in very small amounts in the adrenal. The central nervous system was not studied. All three persisted longest in the reticulo-endothelial system and the connective tissue, and in the doses employed egg white (10 mg.) was no longer detectable after 1 day, bovine albumin (10 mg.) after 2 days, and human γ-globulin (4 mg.) after 6 days, although in a somewhat higher dose (10 mg.) human γ-globulin persisted longer than 8 days. Egg albumin differed from the others in not being detectable in the cells of the renal glomerulus. It was found that each of the three proteins was present in the nuclei of each cell type enumerated above, often in higher concentration than in the cytoplasm. Further, some of the nuclei not only contained antigen, soon after injection, but were also surrounded by a bright ring associated with the nuclear membrane. By means of photographic records under the fluorescence microscope of sections stained for antigen, and direct observation under the light microscope of the same field subsequently stained with hematoxylin and eosin, it could be determined that the antigen was not adsorbed to chromatin or nucleoli, but was apparently in solution in the nuclear sap.

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Selected References

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  1. COONS A. H., KAPLAN M. H. Localization of antigen in tissue cells; improvements in a method for the detection of antigen by means of fluorescent antibody. J Exp Med. 1950 Jan 1;91(1):1–13. doi: 10.1084/jem.91.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. CRAMPTON C. F., HAUROWITZ F. The intracellular distribution in rabbit liver of injected antigens labeled with I131. Science. 1950 Sep 15;112(2907):300–302. doi: 10.1126/science.112.2907.300. [DOI] [PubMed] [Google Scholar]
  3. GITLIN D. Distribution of azo-proteins in the tissues of the normal mouse. Proc Soc Exp Biol Med. 1950 May;74(1):138–142. doi: 10.3181/00379727-74-17834. [DOI] [PubMed] [Google Scholar]
  4. HILL A. G. S., DEANE H. W., COONS A. H. Localization of antigen in tissue cells; V. Capsular polysaccharide of Friedländer bacillus, type B, in the mouse. J Exp Med. 1950 Jul 1;92(1):35–44. doi: 10.1084/jem.92.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Harris T. N., Ehrich W. E. THE FATE OF INJECTED PARTICULATE ANTIGENS IN RELATION TO THE FORMATION OF ANTIBODIES. J Exp Med. 1946 Jul 31;84(2):157–165. [PMC free article] [PubMed] [Google Scholar]
  6. Hawn C. V., Janeway C. A. HISTOLOGICAL AND SEROLOGICAL SEQUENCES IN EXPERIMENTAL HYPERSENSITIVITY. J Exp Med. 1947 May 31;85(6):571–590. doi: 10.1084/jem.85.6.571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Heidelberger M., Kendall F. E. A QUANTITATIVE THEORY OF THE PRECIPITIN REACTION : III. THE REACTION BETWEEN CRYSTALLINE EGG ALBUMIN AND ITS HOMOLOGOUS ANTIBODY. J Exp Med. 1935 Oct 31;62(5):697–720. doi: 10.1084/jem.62.5.697. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. KAPLAN M. E., COONS A. H., DEANE H. W. Localization of antigen in tissue cells; cellular distribution of pneumococcal polysaccharides types II and III in the mouse. J Exp Med. 1950 Jan 1;91(1):15-30, 4 pl. doi: 10.1084/jem.91.1.15. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. 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]
  10. Landsteiner K. SEROLOGICAL REACTIVITY OF HYDROLYTIC PRODUCTS FROM SILK. J Exp Med. 1942 Mar 1;75(3):269–276. doi: 10.1084/jem.75.3.269. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. OLIVER J. The structure of the metabolic process in the nephron. J Mt Sinai Hosp N Y. 1948 Nov–Dec;15(4):175–222. [PubMed] [Google Scholar]
  12. 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]
  13. Schechtman A. M., Nishihara T. Serological Relationships between Nucleus, Cytoplasm, and Cytoplasmic Products and the Concept of Complementary Molecules. Science. 1950 Apr 7;111(2884):357–359. doi: 10.1126/science.111.2884.357. [DOI] [PubMed] [Google Scholar]
  14. Smetana H. The Permeability of the Renal Glomeruli of Several Mammalian Species to Labelled Proteins. Am J Pathol. 1947 Mar;23(2):255–267. [PMC free article] [PubMed] [Google Scholar]

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