Skip to main content
The Journal of Experimental Medicine logoLink to The Journal of Experimental Medicine
. 1981 Nov 1;154(5):1261–1278. doi: 10.1084/jem.154.5.1261

T cell receptors with allo-major histocompatibility complex specificity from rat and mouse. Similarity of size, plasmin susceptibility, and localization of antigen-binding region

PMCID: PMC2186512  PMID: 6170713

Abstract

Antisera specific for the constant part Ctau of T cell receptor molecules in mice and rats have been produced in rabbits by immunization with idiotype-positive rat T cell molecules. Such antisera could be shown to react with the majority of normal T lymphocytes from both rats and mice. Mixed leukocyte culture-activated T blasts displayed a higher percentage of positive cells than concanovalin A- or phytohemaglutinin-induced T blasts. Lipopolysaccharide-induced B blasts were not reactive with the antiserum. Lyt-1-,2+,3+ blasts displayed a significantly brighter straining than the corresponding Lyt-1+,2-,3- blasts. Isolation of the reactive molecules from T cells by immunosorption yielded a 70,000-dalton single chain polypeptide as the dominant group of molecules. Plasmin caused the chain to split into 45,000- and 25,000-dalton polypeptides, with the smaller fragment displaying antigen-binding capacity. Molecules identical in size and plasma degradation patterns were isolated from Lyt-1+,2-3- and 1-,2+,3+ blasts. Preliminary functional data supported the view that the antiserum is directed against the constant region Ctau relevant receptor structures on immunocompetent T lymphocytes.

Full Text

The Full Text of this article is available as a PDF (1.4 MB).

Selected References

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

  1. Anker H. S. A solubilizable acrylamide gel for electrophoresis. FEBS Lett. 1970 Apr 16;7(3):293–293. doi: 10.1016/0014-5793(70)80185-5. [DOI] [PubMed] [Google Scholar]
  2. Bach B. A., Greene M. I., Benacerraf B., Nisonoff A. Mechanisms of regulation of cell-mediated immunity. IV. Azobenzenearsonate-specific suppressor factor(s) bear cross-reactive idiotypic determinants the expression of which is linked to the heavy-chain allotype linkage group of genes. J Exp Med. 1979 May 1;149(5):1084–1098. doi: 10.1084/jem.149.5.1084. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Binz H., Frischknecht H., Shen F. W., Wigzell H. Idiotypic determinants on T-cell subpopulations. J Exp Med. 1979 Apr 1;149(4):910–922. doi: 10.1084/jem.149.4.910. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Binz H., Wigzell H., Bazin H. T-cell idiotypes are linked to immunoglobulin heavy chain genes. Nature. 1976 Dec 16;264(5587):639–642. doi: 10.1038/264639a0. [DOI] [PubMed] [Google Scholar]
  5. Binz H., Wigzell H. Idiotypic, alloantigen-reactive T lymphocyte receptors and their use to induce specific transplantation tolerance. Prog Allergy. 1977;23:154–198. [PubMed] [Google Scholar]
  6. Binz H., Wigzell H. Shared idiotypic determinants on B and T lymphocytes reactive against the same antigenic determinants. I. Demonstration of similar or identical idiotypes on IgG molecules and T-cell receptors with specificity for the same alloantigens. J Exp Med. 1975 Jul 1;142(1):197–211. doi: 10.1084/jem.142.1.197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Binz H., Wigzell H. Shared idiotypic determinants on B and T lymphocytes reactive against the same antigenic determinants. II. Determination of frequency and characteristics of idiotypic T and B lymphocytes in normal rats using direct visualization. J Exp Med. 1975 Nov 1;142(5):1218–1230. doi: 10.1084/jem.142.5.1218. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Binz H., Wigzell H. Shared idiotypic determinants on B and T lymphocytes reactive against the same antigenic determinants. III. Physical fractionation of specific immunocompetent T lymphocytes by affinity chromatography using anti-idiotypic antibodies. J Exp Med. 1975 Nov 1;142(5):1231–1240. doi: 10.1084/jem.142.5.1231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Binz H., Wigzell H. Shared idiotypic determinants on B and T lymphocytes reactive against the same antigenic determinants. V. Biochemical and serological characteristics of naturally occurring, soluble antigen-binding T-lymphocyte-derived molecules. Scand J Immunol. 1976;5(5):559–571. doi: 10.1111/j.1365-3083.1976.tb00311.x. [DOI] [PubMed] [Google Scholar]
  10. Brondz B. D. Complex specificity of immune lymphocytes in allogeneic cell cultures. Folia Biol (Praha) 1968;14(2):115–131. [PubMed] [Google Scholar]
  11. Crone M., Koch C., Simonsen M. The elusive T cell receptor. Transplant Rev. 1972;10:36–56. doi: 10.1111/j.1600-065x.1972.tb01538.x. [DOI] [PubMed] [Google Scholar]
  12. Dorval G., Welsh K. I., Wigzell H. A radioimmunoassay of cellular surface antigens on living cells using iodinated soluble protein A from Staphylococcus aureus. J Immunol Methods. 1975 Jun;7(2-3):237–250. doi: 10.1016/0022-1759(75)90021-6. [DOI] [PubMed] [Google Scholar]
  13. Eichmann K., Ben-Neriah Y., Hetzelberger D., Polke C., Givol D., Lonai P. Correlated expression of VH framework and VH idiotypic determinants on T helper cells and on functionally undefined T cells binding group A streptococcal carbohydrate. Eur J Immunol. 1980 Feb;10(2):105–112. doi: 10.1002/eji.1830100207. [DOI] [PubMed] [Google Scholar]
  14. Eichmann K., Rajewsky K. Induction of T and B cell immunity by anti-idiotypic antibody. Eur J Immunol. 1975 Oct;5(10):661–666. doi: 10.1002/eji.1830051002. [DOI] [PubMed] [Google Scholar]
  15. Feldmann M., Beverley P., Erb P., Howie S., Kontiainen S., Maoz A., Mathies M., McKenzie I., Woody J. Current concepts of the antibody response: heterogeneity of lymphoid cells, interactions, and factors. Cold Spring Harb Symp Quant Biol. 1977;41(Pt 1):113–118. doi: 10.1101/sqb.1977.041.01.015. [DOI] [PubMed] [Google Scholar]
  16. Fenner M., Frischknecht H., Binz H., Lindenmann J., Wigzell H. Alloantigens derived from stimulator cells and bound onto MLC-activated rat T lymphoblasts. Scand J Immunol. 1979;9(6):553–562. doi: 10.1111/j.1365-3083.1979.tb03284.x. [DOI] [PubMed] [Google Scholar]
  17. Fresno M., Mc-Vay Boudreau L., Nabel G., Cantor H. Biologic properties of a purified antigen-specific suppressive glycopeptide. Transplant Proc. 1981 Mar;13(1 Pt 2):1124–1127. [PubMed] [Google Scholar]
  18. Frischknecht H., Binz H., Wigzell H. Induction of specific transplantation immune reactions using anti-idiotypic antibodies. J Exp Med. 1978 Feb 1;147(2):500–514. doi: 10.1084/jem.147.2.500. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Germain R. N., Ju S. T., Kipps T. J., Benacerraf B., Dorf M. E. Shared idiotypic determinants on antibodies and T-cell-derived suppressor factor specific for the random terpolymer L-glutamic acid60-L-alanine30-L-tyrosine10. J Exp Med. 1979 Mar 1;149(3):613–622. doi: 10.1084/jem.149.3.613. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Golstein P., Erik M. D., Svedmyr A. J., Wigzell H. Cells mediating specific in vitro cytotoxicity. I. Detection of receptor-bearing lymphocytes. J Exp Med. 1971 Dec 1;134(6):1385–1402. doi: 10.1084/jem.134.6.1385. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Hengartner H., Meo T., Müller E. Assignment of genes for immunoglobulin kappa and heavy chains to chromosomes 6 and 12 in mouse. Proc Natl Acad Sci U S A. 1978 Sep;75(9):4494–4498. doi: 10.1073/pnas.75.9.4494. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Hämmerling G. J., Black S. J., Berek C., Eichmann K., Rajewsky K. Idiotypic analysis of lymphocytes in vitro. II. Genetic control of T-helper cell responsiveness to anti-idiotypic antibody. J Exp Med. 1976 Apr 1;143(4):861–869. doi: 10.1084/jem.143.4.861. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Kimura A. K. Inhibition of specific cell-mediated cytotoxicity by anti-T-cell receptor antibody. J Exp Med. 1974 Apr 1;139(4):888–901. doi: 10.1084/jem.139.4.888. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Kontiainen S., Feldmann M. Structural characteristics of antigen-specific suppressor factors: definition of 'constant' region and 'variable' region determinants. Thymus. 1979 Sep;1(1-2):59–79. [PubMed] [Google Scholar]
  25. Krawinkel U., Cramer M., Berek C., Hämmerling G., Black S. J., Rajewsky K., Eichmann K. On the structure of the T-cell receptor for antigen. Cold Spring Harb Symp Quant Biol. 1977;41(Pt 1):285–294. doi: 10.1101/sqb.1977.041.01.034. [DOI] [PubMed] [Google Scholar]
  26. Kurosawa Y., von Boehmer H., Haas W., Sakano H., Trauneker A., Tonegawa S. Identification of D segments of immunoglobulin heavy-chain genes and their rearrangement in T lymphocytes. Nature. 1981 Apr 16;290(5807):565–570. doi: 10.1038/290565a0. [DOI] [PubMed] [Google Scholar]
  27. Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970 Aug 15;227(5259):680–685. doi: 10.1038/227680a0. [DOI] [PubMed] [Google Scholar]
  28. Miller J. F., Mitchell G. F. Thymus and antigen-reactive cells. Transplant Rev. 1969;1:3–42. doi: 10.1111/j.1600-065x.1969.tb00135.x. [DOI] [PubMed] [Google Scholar]
  29. Nabel G., Fresno M., Chessman A., Cantor H. Use of cloned populations of mouse lymphocytes to analyze cellular differentiation. Cell. 1981 Jan;23(1):19–28. doi: 10.1016/0092-8674(81)90266-x. [DOI] [PubMed] [Google Scholar]
  30. Nisbet N. W., Simonsen M., Zaleski M. The frequency of antigen-sensitive cells in tissue transplantation. A commentary on clonal selection. J Exp Med. 1969 Mar 1;129(3):459–467. doi: 10.1084/jem.129.3.459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Owen F. L. Polyclonal activation of Ts cells with antiserum directed against an IGH-1 linked candidate for a T-cell receptor constant region marker. J Supramol Struct. 1980;14(2):175–182. doi: 10.1002/jss.400140206. [DOI] [PubMed] [Google Scholar]
  32. Owen F. L., Riblet R., Taylor B. A. The T suppressor cell alloantigen Tsud maps near immunoglobulin allotype genes and may be an heavy chain constant-region marker on a T cell receptor. J Exp Med. 1981 Apr 1;153(4):801–810. doi: 10.1084/jem.153.4.801. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Pacifico A., Capra J. D. T cell hybrids with arsonate specificity. I. Initial characterization of antigen-specific T cell products that bear a cross-reactive idiotype and determinants encoded by the murine major histocompatibility complex. J Exp Med. 1980 Nov 1;152(5):1289–1301. doi: 10.1084/jem.152.5.1289. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Raff M. C., Feldmann M., De Petris S. Monospecificity of bone marrow-derived lymphocytes. J Exp Med. 1973 Apr 1;137(4):1024–1030. doi: 10.1084/jem.137.4.1024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Sunday M. E., Benacerraf B., Dorf M. E. Hapten-specific T cell responses to 4-hydroxy-3-nitrophenyl acetyl. VI. Evidence for different T cell receptors in cells that mediate H-21-restricted and H-2D-restricted cutaneous sensitivity responses. J Exp Med. 1980 Dec 1;152(6):1554–1562. doi: 10.1084/jem.152.6.1554. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Sunday M. E., Benacerraf B., Dorf M. E. Hapten-specific T cell responses to 4-hydroxy-3-nitrophenyl acetyl. VIII. Suppressor cell pathways in cutaneous sensitivity responses. J Exp Med. 1981 Apr 1;153(4):811–822. doi: 10.1084/jem.153.4.811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Taniguchi M., Saito T., Tada T. Antigen-specific suppressive factor produced by a transplantable I-J bearing T-cell hybridoma. Nature. 1979 Apr 5;278(5704):555–558. doi: 10.1038/278555a0. [DOI] [PubMed] [Google Scholar]
  38. Thèze J., Waltenbaugh C., Dorf M. E., Benacerraf B. Immunosuppressive factor(s) specific for L-glutamic acid50-L-tyrosine50 (GT) II. Presence of I-J determinants on the GT-suppressive factor. J Exp Med. 1977 Jul 1;146(1):287–292. doi: 10.1084/jem.146.1.287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Valbuena O., Marcu K. B., Croce C. M., Huebner K., Weigert M., Perry R. P. Chromosomal locations of mouse immunoglobulin genes. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2883–2887. doi: 10.1073/pnas.75.6.2883. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Wigzell H., Andersson B. Cell separation on antigen-coated columns. Elimination of high rate antibody-forming cells and immunological memory cells. J Exp Med. 1969 Jan 1;129(1):23–36. doi: 10.1084/jem.129.1.23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Wilson D. B., Blyth JL NOWELL P. C. Quantitative studies on the mixed lymphocyte interaction in rats. 3. Kinetics of the response. J Exp Med. 1968 Nov 1;128(5):1157–1181. doi: 10.1084/jem.128.5.1157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Zinkernagel R. M., Doherty P. C. MHC-restricted cytotoxic T cells: studies on the biological role of polymorphic major transplantation antigens determining T-cell restriction-specificity, function, and responsiveness. Adv Immunol. 1979;27:51–177. doi: 10.1016/s0065-2776(08)60262-x. [DOI] [PubMed] [Google Scholar]

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

RESOURCES