The fundamental goal of this proposal is to investigate how human B cell activation and growth are regulated through cell surface molecules. We will focus on characterizing the ligands and signal transduction pathways induced via three major B cell-associated surface molecules, namely CD20, CD40 and Bgp95. We will make use of a set of agonistic monoclonal antibodies (mAb) to these markers and full length cDNAs in expression vectors encoding CD20 and CD40.
Our specific aims are:
Aim 1) to define the ligands for CD20 and CD40, making use of cell lines transformed with either CD20 or CD40;
Aim 2) to characterize the signal transduction pathways for CD20 and CD40 by measuring inositol phospholipid metabolism, protein kinases and/or anti-CD40;
Aim 3) to isolate cDNAs encoding Bgp95 for use in characterizing the structure and function of this surface molecule involved in the regulation of B cell activation;
and Aim 4) to assess the role that the membrane protein tyrosine phosphatase (PTPase) CD45 plays in regulating competence (CD20, Bgp95) and progression (CD40) signals in human B cells. These studies will help to elucidate not only the basic mechanisms regulating small resting B cells, but will also provide new information on how the transition of G0 to the Gl phase of the cell cycle is controlled.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM037905-05
Application #
3293717
Study Section
Immunobiology Study Section (IMB)
Project Start
1986-12-01
Project End
1994-11-30
Budget Start
1991-01-01
Budget End
1991-12-31
Support Year
5
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Richards, Sabrina M; Clark, Edward A (2009) BCR-induced superoxide negatively regulates B-cell proliferation and T-cell-independent type 2 Ab responses. Eur J Immunol 39:3395-403
Ma, Daphne Y; Clark, Edward A (2009) The role of CD40 and CD154/CD40L in dendritic cells. Semin Immunol 21:265-72
Watanabe, Chie; Shu, Geraldine L; Zheng, Timothy S et al. (2008) Caspase 6 regulates B cell activation and differentiation into plasma cells. J Immunol 181:6810-9
Richards, Sabrina; Watanabe, Chie; Santos, Lorna et al. (2008) Regulation of B-cell entry into the cell cycle. Immunol Rev 224:183-200
Craxton, Andrew; Draves, Kevin E; Clark, Edward A (2007) Bim regulates BCR-induced entry of B cells into the cell cycle. Eur J Immunol 37:2715-22
Acosta-Rodriguez, Eva V; Craxton, Andrew; Hendricks, Deborah W et al. (2007) BAFF and LPS cooperate to induce B cells to become susceptible to CD95/Fas-mediated cell death. Eur J Immunol 37:990-1000
Paterson, Jennifer C; Tedoldi, Sara; Craxton, Andrew et al. (2006) The differential expression of LCK and BAFF-receptor and their role in apoptosis in human lymphomas. Haematologica 91:772-80
Graves, Jonathan D; Craxton, Andrew; Clark, Edward A (2004) Modulation and function of caspase pathways in B lymphocytes. Immunol Rev 197:129-46
Craxton, Andrew; Magaletti, Dario; Ryan, Elizabeth J et al. (2003) Macrophage- and dendritic cell--dependent regulation of human B-cell proliferation requires the TNF family ligand BAFF. Blood 101:4464-71
Olson, N Eric; Graves, Jonathan D; Shu, Geraldine L et al. (2003) Caspase activity is required for stimulated B lymphocytes to enter the cell cycle. J Immunol 170:6065-72

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