Humoral immunostimulation. IV. Role of complement
Abstract
When L cells were treated with anti-L-cell antibody in medium containing heat-inactivated fetal calf serum, nucleoside uptake and cell growth were stimulated. The response was markedly increased when fresh, unheated sera from calves, guinea pigs, humans, mice, or rabbits were also present. The factors in unheated serum responsible for the enhancement of immunostimulation were studied. Using low concentrations of sera deficient in various complement (C) components and low concentrations of antibody no augmentation of immunostimulation was seen with Clr-deficient human serum, C2-deficient human serum, C2,4-deficient human serum, C4-deficient guinea pig serum, C3-C9-depleted guinea pig serum (by administration of cobra venom factor to animals), but stimulation was observed with C5-deficient human serum, C5-deficient mouse serum, and C6-deficient rabbit serum. When the concentration of anti-serum was raised, however, augmentation was observed with C4-deficient guinea pig serum. Thus, at low concentrations of antiserum enhancement appeared to occur through the classical C pathway, whereas at high concentrations of antibody either the classical or alternate C pathways appeared to be involved. Stimulation was specifically restored by purified C2 in C2-deficient serum and by C3 in C3-C9-deficient serum. Under the usual reaction conditions consumption of guinea pig C component C4 could be demonstrated which provided direct evidence for activation of the classical C pathway under conditions leading to immunostimulation. By immunofluorescence, cells treated with antibody and normal human serum had human C3 deposited at the cell surface. Taken together these observations suggest that C activated through C3 by either the classical or alternate pathways has the potential to enhance nucleoside incorporation into DNA and cell growth of cells exposed to limiting amounts of antibody. Although the mechanism of stimulation is unknown, it is likely to involve a direct effect of C3 at the level of the cell membrane.
Similar articles
-
Humoral immunostimulation. VI. Increased calcium uptake by cells treated with antibody and complement.J Immunol. 1976 Sep;117(3):973-80. J Immunol. 1976. PMID: 956662
-
Activation of the alternative complement pathway by Leishmania promastigotes: parasite lysis and attachment to macrophages.J Immunol. 1984 Mar;132(3):1501-5. J Immunol. 1984. PMID: 6363545
-
Effect of selective complement deficiency on the rate of neutralization of enveloped viruses by human sera.J Immunol. 1977 Jan;118(1):28-34. J Immunol. 1977. PMID: 187701
-
Antibody and complement modulation of tumor cell growth in vitro and in vivo.Fed Proc. 1978 Aug;37(10):2385-9. Fed Proc. 1978. PMID: 354972 Review.
-
Complement, membrane glycoproteins, and complement receptors: their role in regulation of the immune response.Clin Immunol Immunopathol. 1986 Jul;40(1):94-104. doi: 10.1016/0090-1229(86)90072-3. Clin Immunol Immunopathol. 1986. PMID: 2941194 Review.
Cited by
-
Incorporation of fatty acids into phospholipids in L cells stimulated by antibody.Lipids. 1984 Apr;19(4):239-49. doi: 10.1007/BF02534451. Lipids. 1984. PMID: 6425590
-
Humoral immunostimulation. V. Selection of variant cell lines.J Exp Med. 1975 Nov 1;142(5):1133-49. doi: 10.1084/jem.142.5.1133. J Exp Med. 1975. PMID: 1194850 Free PMC article.
-
Complement inhibition in cancer therapy.Semin Immunol. 2013 Feb;25(1):54-64. doi: 10.1016/j.smim.2013.04.001. Epub 2013 May 24. Semin Immunol. 2013. PMID: 23706991 Free PMC article. Review.
-
Synthesis of lipids or lipid-containing macromolecules in tumor cells. Relevance to host defense.Surv Immunol Res. 1983;2(2):122-8. doi: 10.1007/BF02918569. Surv Immunol Res. 1983. PMID: 6316456 Review. No abstract available.
-
Distinct receptor and regulatory properties of recombinant mouse complement receptor 1 (CR1) and Crry, the two genetic homologues of human CR1.J Exp Med. 1992 Jan 1;175(1):121-9. doi: 10.1084/jem.175.1.121. J Exp Med. 1992. PMID: 1730912 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous