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. 1973 Dec;73(3):549–568.

The Importance of the Included Serum Proteins in the Immune Response in Rabbits to a Rat Skin Xenograft

Cecil A Krakower, Seymour A Greenspon
PMCID: PMC1904097  PMID: 4271965

Abstract

Various substances were isolated from rat skin including, protein-dermatan sulfate, certain other species of heavy and light protein-mucopolysaccharides, five electrophoretically separable nonstructural glycoproteins and a crude and two “purified” variants of structural glycoproteins. When the serum proteins contaminating these substances were removed as completely as possible, none of these produced an accelerated immune response to a rat skin graft in appropriately preimmunized rabbits, and none of those that were tested had a blocking effect on the immune response. On the other hand, the contaminated products and undenatured and denatured rat serum produced accelerated immune responses to a rat skin graft in appropriately preimmunized rabbits. These observations, together with those on skin reactions to the isolated products and to rat serum in rabbits sensitized by rat skin grafts, emphasize the importance of the included serum proteins in the immune response to this type of xenograft.

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Selected References

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  1. BITTER T., MUIR H. M. A modified uronic acid carbazole reaction. Anal Biochem. 1962 Oct;4:330–334. doi: 10.1016/0003-2697(62)90095-7. [DOI] [PubMed] [Google Scholar]
  2. GERBER B. R., FRANKLIN E. C., SCHUBERT M. Ultracentrifugal fractionation of bovine nasal chondromucoprotein. J Biol Chem. 1960 Oct;235:2870–2875. [PubMed] [Google Scholar]
  3. GLICK D., GRUNBAUM B. W. Studies in histochemistry. XLV. Determination of hydroxyproline in microgram amounts of tissue. Arch Biochem Biophys. 1956 Nov;65(1):260–267. doi: 10.1016/0003-9861(56)90192-8. [DOI] [PubMed] [Google Scholar]
  4. GREEN J. P., ROBINSON J. D., Jr Cerebroside sulfate (sulfatide A) in some organs of the rat and in a mast cell tumor. J Biol Chem. 1960 Jun;235:1621–1624. [PubMed] [Google Scholar]
  5. Graf B., de Kozak Y., Pouliquen Y., Calvet M. A., Faure J. P. Ultrastructural study of the resorption of corneal xenografts in rabbits. Exp Eye Res. 1972 Nov;14(3):283–288. doi: 10.1016/0014-4835(72)90015-2. [DOI] [PubMed] [Google Scholar]
  6. Leibowitz H. M., Luzzio A. J. Transplantation antigens in keratoplasty. I. Isolation of a soluble fraction with transplantation antigen activity. Arch Ophthalmol. 1970 Feb;83(2):215–222. doi: 10.1001/archopht.1970.00990030217016. [DOI] [PubMed] [Google Scholar]
  7. Leibowitz H. M., Luzzio A. J. Transplantation antigens in xenogeneic keratoplasty. II. Insoluble corneal fractions. Arch Ophthalmol. 1970 Nov;84(5):645–649. doi: 10.1001/archopht.1970.00990040647018. [DOI] [PubMed] [Google Scholar]
  8. MALAWISTA I., SCHUBERT M. Chondromucoprotein: new extraction method and alkaline degradation. J Biol Chem. 1958 Jan;230(1):535–544. [PubMed] [Google Scholar]
  9. Moczar M., Robert L. Extraction and fractzonation of the media of the thoracic aorta: isolation and characterization of structural glycoproteins. Atherosclerosis. 1970 Jan-Feb;11(1):7–25. doi: 10.1016/0021-9150(70)90004-3. [DOI] [PubMed] [Google Scholar]
  10. NEUMAN R. E., LOGAN M. A. The determination of hydroxyproline. J Biol Chem. 1950 May;184(1):299–306. [PubMed] [Google Scholar]
  11. Nerenberg S. T., Ganger C., DeMarco L. Rapid fluorescent "staining" of nondenatured protein bands in agar and polyacrylamide gels. Anal Biochem. 1971 Oct;43(2):564–574. doi: 10.1016/0003-2697(71)90288-0. [DOI] [PubMed] [Google Scholar]
  12. Nerenberg S. T., Pogojeff G. Liebig condenser disk electrophoresis. Am J Clin Pathol. 1969 Feb;51(2):229–237. doi: 10.1093/ajcp/51.2.229. [DOI] [PubMed] [Google Scholar]
  13. Pal S., Doganges P. T., Schubert M. The separation of new forms of the proteinpolysaccharides of bovine nasal cartilage. J Biol Chem. 1966 Sep 25;241(18):4261–4266. [PubMed] [Google Scholar]
  14. Perper R. J., Okimoto J. T., Cochrum K. C., Ramsey N., Najarian J. S. A rapid method for purification of large quantities of anti-lymphocytic serum. Proc Soc Exp Biol Med. 1967 Jun;125(2):575–580. doi: 10.3181/00379727-125-32150. [DOI] [PubMed] [Google Scholar]
  15. RADHAKRISHNAMURTHY B., FISHKIN A. F., HUBBELL G. J., BERENSON G. S. FURTHER STUDIES OF GLYCOPROTEINS FROM A CARDIOVASCULAR CONNECTIVE TISSUE. Arch Biochem Biophys. 1964 Jan;104:19–26. doi: 10.1016/s0003-9861(64)80029-1. [DOI] [PubMed] [Google Scholar]
  16. Robert L., Payrau P., Pouliquen Y., Parlebras J., Robert B. Role of a structural glycoprotein of corneal stroma in transplantation immunity. Nature. 1965 Jul 24;207(995):383–385. doi: 10.1038/207383a0. [DOI] [PubMed] [Google Scholar]
  17. Stroehmann I., DeWitt C. W. Rat transplantation antigens. I. Extraction and partial purification of a soluble antigen. Immunology. 1972 Dec;23(6):921–928. [PMC free article] [PubMed] [Google Scholar]
  18. Toole B. P., Lowther D. A. Dermatan sulfate-protein: isolation from and interaction with collagen. Arch Biochem Biophys. 1968 Dec;128(3):567–578. doi: 10.1016/0003-9861(68)90064-7. [DOI] [PubMed] [Google Scholar]

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