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International Journal of Experimental Pathology logoLink to International Journal of Experimental Pathology
. 1993 Jun;74(3):259–266.

Binding of the two polypeptide chains of dengue virus-induced suppressor cytokine to its receptor isolated from macrophages.

R Mukherjee 1, P Chaturvedi 1, U C Chaturvedi 1
PMCID: PMC2002161  PMID: 8334075

Abstract

Dengue type 2 virus (DV)-induced suppressor cytokine (SF) is composed of two polypeptide chains (alpha and beta) and has a receptor on macrophages (M phi), which has been purified. The present study was undertaken to study the binding of the two polypeptide chains of SF to M phi and its purified receptor (SF-R) protein. It was observed that both alpha and beta-chains of SF, purified by high performance liquid chromatography (HPLC), bound to M phi cell, but only alpha-chain bound to SF-R protein. Only H-2A positive M phi bound SF. Anti-H-2Ak mAb blocked the binding of SF to M phi but had no effect on binding of SF to SF-R. Both anti-SF-antiserum and anti-SF-R-antiserum blocked the binding of SF to M phi. The binding of the beta-chain of SF to M phi was blocked by anti-H-2Ak mAb while the anti-SF-R-antiserum blocked the binding of alpha-chain on M phi. Thus, the alpha-chain of SF binds to SF-R and the beta-chain binds to H-2A determinants on M phi.

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Selected References

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

  1. Chaturvedi P., Mukherjee R., Chaturvedi U. C., Mathur A. Dengue virus-induced helper cytokine has two polypeptide chains which bear different determinants. Int J Exp Pathol. 1991 Dec;72(6):665–672. [PMC free article] [PubMed] [Google Scholar]
  2. Chaturvedi U. C., Bhargava A., Mathur A. Production of cytotoxic factor in the spleen of dengue virus-infected mice. Immunology. 1980 Aug;40(4):665–671. [PMC free article] [PubMed] [Google Scholar]
  3. Chaturvedi U. C., Nagar R., Gulati L., Mathur A. Variable effects of dengue virus-induced cytotoxic factors on different subpopulations of macrophages. Immunology. 1987 Jul;61(3):297–301. [PMC free article] [PubMed] [Google Scholar]
  4. Chaturvedi U. C., Pahwa M., Mathur A. Dengue virus-induced helper T cells. Indian J Med Res. 1987 Jul;86:1–8. [PubMed] [Google Scholar]
  5. Chaturvedi U. C., Shukla M. I., Mathur A. Role of macrophages in the transmission of dengue virus-induced suppressor signal to a subpopulation of T lymphocytes. Ann Immunol (Paris) 1982 Jan-Feb;133C(1):83–96. doi: 10.1016/0769-2625(82)90008-3. [DOI] [PubMed] [Google Scholar]
  6. JERNE N. K., NORDIN A. A. Plaque formation in agar by single antibody-producing cells. Science. 1963 Apr 26;140(3565):405–405. [PubMed] [Google Scholar]
  7. Jayaraman S., Bellone C. J. Hapten-specific responses to the phenyltrimethylamino hapten. V. A single chain antigen-binding I-J+ first-order T suppressor factor requires antigen to induce anti-idiotypic second-order suppressor T cells. J Immunol. 1985 Feb;134(2):1010–1018. [PubMed] [Google Scholar]
  8. Kapp J. A., Sorensen C. M., Pierce C. W. Antigen-specific suppressor T cell interactions. II. Characterization of two different types of suppressor T cell factors specific for L-glutamic acid50-L-tyrosine50 (GT) and L-glutamic acid60-L-alanine30-L-tyrosine10 (GAT). J Exp Med. 1983 Dec 1;158(6):1962–1978. doi: 10.1084/jem.158.6.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Khanna M., Chaturvedi U. C. Purification and amino-terminal sequence of the dengue virus-induced cytotoxic factor. Int J Exp Pathol. 1992 Feb;73(1):43–49. [PMC free article] [PubMed] [Google Scholar]
  10. Klyczek K. K., Cantor H., Hayes C. E. T cell surface I-J glycoprotein. Concerted action of chromosome-4 and -17 genes forms an epitope dependent on alpha-D-mannosyl residues. J Exp Med. 1984 Jun 1;159(6):1604–1617. doi: 10.1084/jem.159.6.1604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Krupen K., Araneo B. A., Brink L., Kapp J. A., Stein S., Wieder K. J., Webb D. R. Purification and characterization of a monoclonal T-cell suppressor factor specific for poly(LGlu60LAla30LTyr10). Proc Natl Acad Sci U S A. 1982 Feb;79(4):1254–1258. doi: 10.1073/pnas.79.4.1254. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. 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]
  13. Noelle R. J., Snow E. C. Cognate interactions between helper T cells and B cells. Immunol Today. 1990 Oct;11(10):361–368. doi: 10.1016/0167-5699(90)90142-v. [DOI] [PubMed] [Google Scholar]
  14. Sanders V. M., Snyder J. M., Uhr J. W., Vitetta E. S. Characterization of the physical interaction between antigen-specific B and T cells. J Immunol. 1986 Oct 15;137(8):2395–2404. [PubMed] [Google Scholar]
  15. Shukla M. I., Chaturvedi U. C. Dengue virus-induced suppressor factor stimulates production of prostaglandin to mediate suppression. J Gen Virol. 1981 Oct;56(Pt 2):241–249. doi: 10.1099/0022-1317-56-2-241. [DOI] [PubMed] [Google Scholar]
  16. Shukla M. I., Chaturvedi U. C. Study of the target cell of the dengue virus-induced suppressor signal. Br J Exp Pathol. 1984 Apr;65(2):267–273. [PMC free article] [PubMed] [Google Scholar]
  17. Shukla M. I., Dalakoti H., Chaturvedi U. C. Ly phenotype of T lymphocytes producing dengue virus-induced immunosuppressive factors. Indian J Exp Biol. 1982 Jul;20(7):525–528. [PubMed] [Google Scholar]

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