Abstract
We have investigated the mechanism(s) by which mitogenic (concanavalin A [Con A], phytohaemagglutinin [PHA] and Lens culinaris agglutinin [LCA]) and non-mitogenic (soybean agglutinin, peanut agglutinin, wheat-germ agglutinin and pokeweed mitogen) lectins mediate, non-specifically, lectin-dependent lymphocytotoxicity (LDCC). We show that non-mitogenic lectins are ineffective mediators of LDCC, due to their inability to mediate effective binding of effector cytotoxic T cells (EC) and target cells (TC), and not to their failure to 'activate' TC-bound EC, as proposed before. Evidence is presented that in LDCC Con A and PHA exert their primary effect(s) by affecting the TC rather than the EC. Although the lectin LCA, unlike Con A and PHA, is equally reactive with either EC or TC, a direct comparison is difficult since the presence of LCA, but not Con A or PHA, during the entire assay is required for optimal kill. Furthermore, all three LDCC-supportive lectins (PHA, Con A and LCA) show a similar TC preference when tested in a EC-TC conjugation assay. Taken together, these results are inconsistent with the theory that lectins mediate LDCC by 'bridging' EC and TC through lectin-binding receptors followed by 'activation' of the TC-bound EC. We would like to suggest that the potential of mitogenic lectins to mediate EC-TC interaction is related to their modification of TC-surface constituents, possibly major histocompatibility complex determinants, rendering them recognizable, non-specifically by EC.
Full text
PDF







Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Berke G., Gabison D. Energy requirements of the binding and lytic steps of T lymphocyte-mediated cytolysis of leukemic cells in vitro. Eur J Immunol. 1975 Oct;5(10):671–675. doi: 10.1002/eji.1830051004. [DOI] [PubMed] [Google Scholar]
- Berke G., Hu V., McVey E., Clark W. R. T lymphocyte-mediated cytolysis. I. A common mechanism for target recognition in specific and lectin-dependent cytolysis. J Immunol. 1981 Aug;127(2):776–781. [PubMed] [Google Scholar]
- Berke G., McVey E., Hu V., Clark W. R. T lymphocyte-mediated cytolysis. II. Role of target cell histocompatibility antigens in recognition and lysis. J Immunol. 1981 Aug;127(2):782–787. [PubMed] [Google Scholar]
- Berke G., Sullivan K. A., Amos B. Rejection of ascites tumor allografts. I. Isolation, characterization, and in vitro reactivity of peritoneal lymphoid effector cells from BALB-c mice immune to EL4 leukosis. J Exp Med. 1972 Jun 1;135(6):1334–1350. doi: 10.1084/jem.135.6.1334. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bernstein D., Klapper D. G., Krause R. M. Use of radioimmunoassays to determine the concentration of streptococcal group-specific antibodies in rabbit antisera. J Immunol. 1975 Jan;114(1 Pt 1):59–63. [PubMed] [Google Scholar]
- Forman J., Möller G. Generation of cytotoxic lymphocytes in mixed lymphocyte reactions. I. Specificity of the effector cells. J Exp Med. 1973 Sep 1;138(3):672–685. doi: 10.1084/jem.138.3.672. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Green W. R., Ballas Z. K., Henney C. S. Studies on the mechanism of lymphocyte-mediated cytolysis. XI. The role of lectin in lectin-dependent cell-mediated cytotoxicity. J Immunol. 1978 Oct;121(4):1566–1572. [PubMed] [Google Scholar]
- Kimura A., Ersson B. Activation of T lymphocytes by lectins and carbohydrate-oxidizing reagents viewed as an immunological recognition of cell-surface modifications seen in the context of "self" major histocompatibility complex antigens. Eur J Immunol. 1981 Jun;11(6):475–483. doi: 10.1002/eji.1830110607. [DOI] [PubMed] [Google Scholar]
- Kuppers R. C., Henney C. S. Studies on the mechanism of lymphocyte-mediated cytolysis. IX. Relationships between antigen recognition and lytic expression in killer T cells. J Immunol. 1977 Jan;118(1):71–76. [PubMed] [Google Scholar]
- Novogrodsky A. Induction of lymphocyte cytotoxicity by modification of the effector or target cells with periodate or with neuraminidase and galactose oxidase. J Immunol. 1975 Mar;114(3):1089–1093. [PubMed] [Google Scholar]
- Novogrodsky A., Katchalski E. Induction of lymphocyte transformation by sequential treatment with neuraminidase and galactose oxidase. Proc Natl Acad Sci U S A. 1973 Jun;70(6):1824–1827. doi: 10.1073/pnas.70.6.1824. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Novogrodsky A., Katchalski E. Membrane site modified on induction of the transformation of lymphocytes by periodate. Proc Natl Acad Sci U S A. 1972 Nov;69(11):3207–3210. doi: 10.1073/pnas.69.11.3207. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Parker W. L., Martz E. Lectin-induced nonlethal adhesions between cytolytic T lymphocytes and antigenically unrecognizable tumor cells and nonspecific "triggering" of cytolysis. J Immunol. 1980 Jan;124(1):25–35. [PubMed] [Google Scholar]
- Schmitt-Verhulst A., Shearer G. M. Effects of sodium periodate modification of lymphocytes on the sensitization and lytic phases of T cell-mediated lympholysis. J Immunol. 1976 Apr;116(4):947–958. [PubMed] [Google Scholar]
