The investigators will study the role of membrane Ig and the function of helper T cells in the antibody response by exploiting a new, murine, in vitro polyclonal model for T cell/B cell cooperation. In this model, rabbit antibody against mouse immunoglobulin (anti-Ig) is used in place of antigen, and T cell help is provided by cultured T cell lines and cloned T cell hybridomas which recognize the rabbit anti-Ig reagents as foreign protein antigens. The investigators have shown that normal, small B cells act as extraordinarily efficient antigen presenting cells for rabbit anti-IgM or anti-IgD. Recognition of anti-Ig on the B cell surface is restricted by class II products of the major histocompatibility complex (MHC), and results in both a T cell response and a vigorous polyclonal B cell response. The model will be used to define the role of membrane Ig in antigen processing (if processing occurs in small B cells) and presentation of specifically bound antigen to helper T cells. Functional heterogeneity of helper T cells in their ability to interact with small B cells or other antigen presenting cells will be defined and explored. The mechanism of delivery of T cell help will be studied to determine whether help can be accounted for by secretion of characterized or novel lymphokines, or requires an early, contact-mediated event involving stimulated secretion of preformed mediators or interaction of membrane- bound molecules other then those required for specific recognition by the T cell. Finally, in an attempt to relate immune cell physiology to the cellular machinery which regulates cell division, the investigators have begun to study the effects of agents which activate B lymphocytes to different extents or by different pathways on the levels of cmyc mRNA in the cell during the first hours of the activation sequence. These studies will be extended to other cellular protooncogenes (c-fos, c-myb, c-ras) and genes induced by growth signals in fibroblasts (JE and KC), and transcription rates will be compared with mRNA levels.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI024303-03
Application #
3137212
Study Section
Allergy and Immunology Study Section (ALY)
Project Start
1987-07-01
Project End
1992-06-30
Budget Start
1989-07-01
Budget End
1990-06-30
Support Year
3
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Type
Schools of Medicine
DUNS #
660735098
City
Worcester
State
MA
Country
United States
Zip Code
01655
Evans, D E; Munks, M W; Purkerson, J M et al. (2000) Resting B lymphocytes as APC for naive T lymphocytes: dependence on CD40 ligand/CD40. J Immunol 164:688-97
Purkerson, J M; Parker, D C (1998) Differential coupling of membrane Ig and CD40 to the extracellularly regulated kinase signaling pathway. J Immunol 160:2121-9
Schrader, C E; Stavnezer, J; Kikutani, H et al. (1997) Cognate T cell help for CD40-deficient B cells induces c-myc RNA expression, but DNA synthesis requires an additional signal through surface Ig. J Immunol 158:153-62
Kawakami, K; Parker, D C (1993) Antigen and helper T lymphocytes activate B lymphocytes by distinct signaling pathways. Eur J Immunol 23:77-84
Klaus, S J; Phillips, N E; Parker, D C (1993) Effects of IL-4 and Fc gamma receptor II engagement on Egr-1 expression during stimulation of B lymphocytes by membrane immunoglobulin crosslinking. Mol Immunol 30:1553-8
Parker, D C (1993) T cell-dependent B cell activation. Annu Rev Immunol 11:331-60
Markowitz, J S; Rogers, P R; Grusby, M J et al. (1993) B lymphocyte development and activation independent of MHC class II expression. J Immunol 150:1223-33
Parker, D C (1993) The functions of antigen recognition in T cell-dependent B cell activation. Semin Immunol 5:413-20
Lalmanach-Girard, A C; Chiles, T C; Parker, D C et al. (1993) T cell-dependent induction of NF-kappa B in B cells. J Exp Med 177:1215-9
Eynon, E E; Parker, D C (1992) Small B cells as antigen-presenting cells in the induction of tolerance to soluble protein antigens. J Exp Med 175:131-8

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