Our laboratory studies the functions of non-receptor tyrosine kinases, molecules required for intracellular signaling pathways involved in normal cellular growth and differentiation as well as abnormal growth and development involved in the formation and progression of cancer. We apply a combination of mouse genetics, cellular biology and protein biochemistry to the study of these molecules. Our work has concentrated on how these molecules contribute to normal function of cells of the immune system and the skeletal system and how lessons we learn from these systems can be extended to other celltypes in which these molecules function. Our recent work has concentrated on studies of the Btk family of kinases. Btk has previously been shown to be required for normal function of B cells and mutation of Btk is responsible for the human genetic disorder X-linked agammmaglobulimemia. We have recently shown that mutation of other Btk family kinases can severely impair T lymphocyte function in mice, thereby establishing for the first time a role for these kinases in T cell mediated immune responses. In particular, we have demonstrated that mutation of two Btk family kinases, Rlk and Itk leads to marked defects in T cell responses to stimulation in culture and to infectious agents in the animal. We have also continued work on the study of Src family kinases in bone cell function. We have recently shown that expression of a truncated mutant of Src can act as a dominant-negative molecule and lead to programmed cell death or apoptosis. We have extended this work to show that this mutant can alter cell survival pathways required for angiogenesis and tumor growth. Recent work has demonstrated that the SH2 (Src homology 2) domain is important for these cell survival pathways. This work provides a model for the use of inhibitors of Src function in the treatment of certain tumors. - Genetics, Immunology, Infectious Diseases, Tropical Diseases, Osteoporosis
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| Chiang, Y Jeffrey; Jordan, Martha S; Horai, Reiko et al. (2009) Cbl enforces an SLP76-dependent signaling pathway for T cell differentiation. J Biol Chem 284:4429-38 |
| Schwartzberg, Pamela L; Mueller, Kristen L; Qi, Hai et al. (2009) SLAM receptors and SAP influence lymphocyte interactions, development and function. Nat Rev Immunol 9:39-46 |
| Steinfelder, Svenja; Andersen, John F; Cannons, Jennifer L et al. (2009) The major component in schistosome eggs responsible for conditioning dendritic cells for Th2 polarization is a T2 ribonuclease (omega-1). J Exp Med 206:1681-90 |
| Sahu, Nisebita; Venegas, Ana M; Jankovic, Dragana et al. (2008) Selective expression rather than specific function of Txk and Itk regulate Th1 and Th2 responses. J Immunol 181:6125-31 |
| Readinger, Julie A; Schiralli, Gillian M; Jiang, Jian-Kang et al. (2008) Selective targeting of ITK blocks multiple steps of HIV replication. Proc Natl Acad Sci U S A 105:6684-9 |
| Schwartzberg, Pamela L (2007) Formin the way. Immunity 26:139-41 |
| Konno, Akihiro; Kirby, Martha; Anderson, Stacie A et al. (2007) The expression of Wiskott-Aldrich syndrome protein (WASP) is dependent on WASP-interacting protein (WIP). Int Immunol 19:185-92 |
| Zhao, Ling; Cannons, Jennifer L; Anderson, Stacie et al. (2007) CBFB-MYH11 hinders early T-cell development and induces massive cell death in the thymus. Blood 109:3432-40 |
| Gomez-Rodriguez, Julio; Readinger, Julie A; Viorritto, Irene C et al. (2007) Tec kinases, actin, and cell adhesion. Immunol Rev 218:45-64 |
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