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. 1979 Oct 1;150(4):830–848. doi: 10.1084/jem.150.4.830

T-lymphocyte response to cytochrome c. I. Demonstration of a T-cell heteroclitic proliferative response and identification of a topographic antigenic determinant on pigeon cytochrome c whose immune recognition requires two complementing major histocompatibility complex-linked immune response genes

PMCID: PMC2185679  PMID: 92520

Abstract

The T-lymphocyte proliferative response to pigeon cytochrome c was studied in the mouse. H-2a and H-2k strains were responders to this antigen whereas H-2b, H-2d, H-2f, H-2ja, H-2p, H-2q, H-2r, H-2s, and H- 2u strains were low or nonresponders. Genetic mapping demonstrated that two major histocompatibility complex (MHC)-linked Ir genes control the response, one in I-A, the other in I-E/I-C. The major antigenic determinant recognized in this response was localized by cross- stimulations with species variants and cyanogen bromide cleavage fragments of cytochrome c. It was found to be a topographic surface determinant composed of an isoleucine for valine substitution at residue 3, a glutamine for lysine substitution at residue 100 and a lysine for glutamic acid substitution at residue 104. Tobacco hornworm moth cytochrome c, which contains a glutamine at residue 100 but a terminal lysine at residue 103 (one amino acid closer to the glutamine), stimulated pigeon cytochrome c immune T cells better than the immunogen. This result demonstrates for the first time a functional T-cell heteroclitic proliferative response in a system under Ir gene control. Immunization with the cyanogen bromide cleavage fragments revealed that only pigeon cytochrome c fragment 81-104 was immunogenic. This fragment primed for a T-cell proliferative response whose specificity was nearly identical to that of the T-cell response primed for by the whole molecule, suggesting that the glutamine at 100 and the lysine at 104 form the immunodominant portion of the antigenic site. Furthermore, mixing experiments using the two cross-reacting antigens, hippopotamus cytochrome c and Pekin duck or chicken cytochrome c fragment (81-104), each of which contains only one of the two immunodominant substitutions, demonstrated that the T lymphocytes responding to the major antigenic determinant comprise a single family of clones that recognize both amino acids as part of the same determinant. Thus, two complementing MHC-linked Ir genes can control the immune response to a single antigenic determinant.

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Selected References

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  1. Barcinski M. A., Rosenthal A. S. Immune response gene control of determinant selection. I. Intramolecular mapping of the immunogenic sites on insulin recognized by guinea pig T and B cells. J Exp Med. 1977 Mar 1;145(3):726–742. doi: 10.1084/jem.145.3.726. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Benacerraf B. A hypothesis to relate the specificity of T lymphocytes and the activity of I region-specific Ir genes in macrophages and B lymphocytes. J Immunol. 1978 Jun;120(6):1809–1812. [PubMed] [Google Scholar]
  3. Brautigan D. L., Ferguson-Miller S., Margoliash E. Mitochondrial cytochrome c: preparation and activity of native and chemically modified cytochromes c. Methods Enzymol. 1978;53:128–164. doi: 10.1016/s0076-6879(78)53021-8. [DOI] [PubMed] [Google Scholar]
  4. Corradin G., Chiller J. M. Lymphocyte specificity to protein antigens. II. Fine specificity of T-cell activation with cytochrome c and derived peptides as antigenic probes. J Exp Med. 1979 Feb 1;149(2):436–447. doi: 10.1084/jem.149.2.436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Corradin G., Harbury H. A. Cleavage of cytochrome c with cyanogen bromide. Biochim Biophys Acta. 1970 Dec 22;221(3):489–496. doi: 10.1016/0005-2795(70)90219-9. [DOI] [PubMed] [Google Scholar]
  6. Dorf M. E., Benacerraf B. Complementation of H-2-linked Ir genes in the mouse. Proc Natl Acad Sci U S A. 1975 Sep;72(9):3671–3675. doi: 10.1073/pnas.72.9.3671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Feldmann R. J., Bing D. H., Furie B. C., Furie B. Interactive computer surface graphics approach to study of the active site of bovine trypsin. Proc Natl Acad Sci U S A. 1978 Nov;75(11):5409–5412. doi: 10.1073/pnas.75.11.5409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. GELL P. G., BENACERRAF B. Studies on hypersensitivity. II. Delayed hypersensitivity to denatured proteins in guinea pigs. Immunology. 1959 Jan;2(1):64–70. [PMC free article] [PubMed] [Google Scholar]
  9. Imanishi T., Mäkelä O. Strain differences in the fine specificity of mouse anti-hapten antibodies. Eur J Immunol. 1973 Jun;3(6):323–330. doi: 10.1002/eji.1830030602. [DOI] [PubMed] [Google Scholar]
  10. Jemmerson R., Margoliash E. Analysis of a complex antigenic site on horse cytochrome c. Adv Exp Med Biol. 1978;98:119–129. doi: 10.1007/978-1-4615-8858-0_6. [DOI] [PubMed] [Google Scholar]
  11. Jones P. P., Murphy D. B., McDevitt H. O. Two-gene control of the expression of a murine Ia antigen. J Exp Med. 1978 Oct 1;148(4):925–939. doi: 10.1084/jem.148.4.925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Keck K. Ir gene control of carrier recognition. III. Cooperative recognition of two or more carrier determinants on insulins of different species. Eur J Immunol. 1977 Nov;7(11):811–816. doi: 10.1002/eji.1830071113. [DOI] [PubMed] [Google Scholar]
  13. Krawinkel U., Cramer M., Melchers I., Imanishi-Kari T., Rajewsky K. Isolated hapten-binding receptors of sensitized lymphocytes. III. Evidence for idiotypic restriction of T-cell receptors. J Exp Med. 1978 May 1;147(5):1341–1347. doi: 10.1084/jem.147.5.1341. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Mandel N., Mandel G., Trus B. L., Rosenberg J., Carlson G., Dickerson R. E. Tuna cytochrome c at 2.0 A resolution. III. Coordinate optimization and comparison of structures. J Biol Chem. 1977 Jul 10;252(13):4619–4636. [PubMed] [Google Scholar]
  15. Margoliash E. The molecular variations of cytochrome c as a function of the evolution of species. Harvey Lect. 1971;66:177–247. [PubMed] [Google Scholar]
  16. McDevitt H. O., Sela M. Genetic control of the antibody response. I. Demonstration of determinant-specific differences in response to synthetic polypeptide antigens in two strains of inbred mice. J Exp Med. 1965 Sep 1;122(3):517–531. doi: 10.1084/jem.122.3.517. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Reichlin M., Eng J. Identifying antigenic determinants on cytochrome C for B and T cells. Adv Exp Med Biol. 1978;98:5–18. doi: 10.1007/978-1-4615-8858-0_2. [DOI] [PubMed] [Google Scholar]
  18. Rosenthal A. S. Determinant selection and macrophage function in genetic control of the immune response. Immunol Rev. 1978;40:136–152. doi: 10.1111/j.1600-065x.1978.tb00404.x. [DOI] [PubMed] [Google Scholar]
  19. Schirrmacher V., Wigzell H. Immune responses against native and chemically modified albumins in mice. II. Effect of electric charge and conformation on the humoral antibody response and on helper T cell responses. J Immunol. 1974 Nov;113(5):1635–1643. [PubMed] [Google Scholar]
  20. Schwartz R. H., Berzofsky J. A., Horton C. L., Schechter A. N., Sachs D. H. Genetic control of the T lymphocyte proliferative response to staphylococcal nuclease: evidence for multiple MHC-linked Ir gene control. J Immunol. 1978 May;120(5):1741–1749. [PubMed] [Google Scholar]
  21. Schwartz R. H., Dorf M. E., Benacerraf B., Paul W. E. The requirement for two complementing Ir-GLphi immune response genes in the T-lymphocyte proliferative response to poly-(Glu53Lys36Phe11). J Exp Med. 1976 Apr 1;143(4):897–905. doi: 10.1084/jem.143.4.897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Schwartz R. H., Paul W. E. T-lymphocyte-enriched murine peritoneal exudate cells. II. Genetic control of antigen-induced T-lymphocyte proliferation. J Exp Med. 1976 Mar 1;143(3):529–540. doi: 10.1084/jem.143.3.529. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Schwartz R. H., Solinger A. M., Ultee M., Margoliash E. Genetic control of the T-lymphocyte proliferative response to cytochrome c. Adv Exp Med Biol. 1978;98:371–386. doi: 10.1007/978-1-4615-8858-0_20. [DOI] [PubMed] [Google Scholar]
  24. Schwartz R. H., Yano A., Stimpfling J. H., Paul W. E. Gene complementation in the T-lymphocyte proliferative response to poly (Glu55Lys36Phe9)n. A demonstration that both immune response gene products must be expressed in the same antigen-presenting cell. J Exp Med. 1979 Jan 1;149(1):40–57. doi: 10.1084/jem.149.1.40. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Sercarz E. E., Yowell R. L., Turkin D., Miller A., Araneo B. A., Adorini L. Different functional specificity repertoires for suppressor and helper T cells. Immunol Rev. 1978;39:108–136. doi: 10.1111/j.1600-065x.1978.tb00398.x. [DOI] [PubMed] [Google Scholar]
  26. Takatsu K., Ishizaka K. Reaginic antibody formation in the mouse. VI. Suppression of IgE and IgG antibody responses to ovalbumin following the administration of high dose urea-denatured antigen. Cell Immunol. 1975 Dec;20(2):276–289. doi: 10.1016/0008-8749(75)90105-7. [DOI] [PubMed] [Google Scholar]
  27. Tanaka N., Yamane T., Tsukihara T., Ashida T., Kakudo M. The crystal structure of bonito (katsuo) ferrocytochrome c at 2.3 A resolution. II. Structure and function. J Biochem. 1975 Jan 1;77(1?):147–162. [PubMed] [Google Scholar]
  28. Toniolo C., Fontana A., Scoffone E. Conformational studies of equilibrium structures in fragments of horse heart cytochrome c. Eur J Biochem. 1975 Jan 2;50(2):367–374. doi: 10.1111/j.1432-1033.1975.tb09812.x. [DOI] [PubMed] [Google Scholar]
  29. Weinberger J. Z., Greene M. I., Benacerraf B., Dorf M. E. Hapten-specific T-cell responses to 4-hydroxy-3-nitrophenyl acetyl. I. Genetic control of delayed-type hypersensitivity by VH and I-A-region genes. J Exp Med. 1979 Jun 1;149(6):1336–1348. doi: 10.1084/jem.149.6.1336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Wolff M. L., Reichlin M. Antigenic specificity of T cell receptors for cytochrome C on guinea pig lymphocytes. Immunochemistry. 1978 May;15(5):289–294. doi: 10.1016/0161-5890(78)90087-1. [DOI] [PubMed] [Google Scholar]

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