The purpose of this project is to study signal transduction and cell cycle progression using neurofibromin-deficient B lymphocytes generated by transferring Nf1-/-fetal liver cells into Rag1-/- mice. The identity of a specific 75-78kD protein, which comigrates with Btk, and which is specifically not phosphorylated on tyrosine residues in antigen receptor- stimulated neurofibromin-deficient B-cells will be determined. The ability of these cells to proliferate in response to antigen receptor crosslinking, CD40 ligation, and IL-4 will be examined. Reconstituted mice will be observed long-term for lymphoproliferation and responses to T- dependent and T-independent antigens will also be examined. Studies will be performed to examine whether neurofibromin plays a role in promoting specific tyrosine phosphorylation events, or whether it is a negative regulator of specific phosphotyrosyl phosphatases. Proteins that specifically associate with neurofibromin in B lymphocytes will be purified.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA069618-02
Application #
2517697
Study Section
Experimental Immunology Study Section (EI)
Project Start
1996-09-01
Project End
1999-08-31
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
2
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Massachusetts General Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02199
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Kim, Tae Jin; Cariappa, Annaiah; Iacomini, John et al. (2002) Defective proliferative responses in B lymphocytes and thymocytes that lack neurofibromin. Mol Immunol 38:701-8
Cariappa, A; Tang, M; Parng, C et al. (2001) The follicular versus marginal zone B lymphocyte cell fate decision is regulated by Aiolos, Btk, and CD21. Immunity 14:603-15
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Cariappa, A; Liou, H C; Horwitz, B H et al. (2000) Nuclear factor kappa B is required for the development of marginal zone B lymphocytes. J Exp Med 192:1175-82
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Ho, S C; Rajagopalan, S; Chaudhuri, S et al. (1999) Membrane anchoring of calnexin facilitates its interaction with its targets. Mol Immunol 36:1-12
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