B cell antigen receptor (BCR) signaling controls the development, selection and function of B lymphocytes. Work in our lab has determined that the lysophospholipid, lysophosphatidic acid (LPA), signals to the LPA5 G-protein coupled receptor expressed by B lineage cells to suppress BCR signaling and subsequent antibody response. LPA binds and signals to LPA receptors with low nanomolar affinity and as a major lysophospholipid is present in blood at high nanomolar to low micromolar concentrations. However, despite that lymphocytes express several LPA receptors;relatively little is understood about how LPA influences humoral immunity. A long-term goal of our research has been to understand how BCR-derived signals intersect with those signals transmitted via GPCRs such as chemoattractant receptors and the goal of this application is to define how LPA signaling through LPA receptors on B lineage cells regulates the development and function of B lymphocytes. LPA has also been characterized as an inflammatory lipid and whose levels are considerably elevated in a number of chronic inflammatory disorders such as cancer, autoimmunity and viral infections. We show that at these heightened LPA levels BCR signaling is further inhibited. Thus, we also investigate how pathophysiological levels of LPA alter B cell tolerance induction in the bone marrow and antibody responses by marginal zone and follicular B cell populations. To address these issues, we propose in vitro and in vivo experiments that rely on well-characterized mouse models of B cell tolerance and antibody response to elucidate the role(s) of LPA receptors on B lymphocytes during their development in the bone marrow and their function as mature B cells in the periphery. These experiments are outlined in the following Specific Aims:
Aim 1 : Characterize how LPA regulates immature B cell development and tolerance induction. 1A. Establish if LPA receptors guide immature B cell localization in the bone marrow during These experiments ask how LPA receptor signaling influence B lymphopoeisis and if pathological LPA levels alters central B cell tolerance.
Aim 2 : Characterize the molecular and cellular mechanisms that lead to LPA suppression of B cell antibody responses. Here we define the extent to which LPA regulates B cell responses and the signaling pathways used by LPA receptors to inhibit BCR signaling. In particular, we determine if antigen-specific B cell responses are suppressed by all antigens or only antigens with certain (weak) affinity.
Aim 3 : Characterize how local autotaxin expression influences LPA regulation of B cell responses and if inflammatory and autoimmune settings alter the regulation of its expression. These experiments are designed to define the relative contributions of locally-restricted LPA production versus global systemic LPA levels in regulating the B cell antibody response and how LPA production may be altered in inflammatory and autoimmune settings. Significance. The sphingosine-1-phosphate (S1P) lysophospholipid has emerged as a critical regulator of lymphocyte development, trafficking and localization. However, lymphocytes and most other cells of the immune system also express G-protein coupled receptors that recognize another major lysophospholipid, lysophosphatidic acid (LPA). In contrast to S1P, that serves an important role under homeostatic conditions, LPA has features of an inflammatory lipid and has been associated with a chronic inflammatory disorders. Notably, how LPA regulates immune function and, specifically, humoral immunity is largely unexplored. The successful completion of these experiments is expected to illustrate how LPA functions to regulate the development, selection and antibody response by B lymphocytes. Furthermore, as LPA-LPA receptor signaling has been associated with a number of different types of cancer and has received considerable attention for possible therapeutic intervention, these findings will also be important to inform on how such strategies might alter adaptive immunity.
B lymphocytes of the immune system are responsible for producing antibodies against foreign pathogens. This application describes experiments that address how a lipid present normally in the blood of healthy individuals regulates how B lymphocytes develop in the bone marrow and eventually produce antibodies to foreign antigens.
|Hu, Jiancheng; Oda, Shannon K; Shotts, Kristin et al. (2014) Lysophosphatidic acid receptor 5 inhibits B cell antigen receptor signaling and antibody response. J Immunol 193:85-95|
|Swanson, Cristina L; Pelanda, Roberta; Torres, Raul M (2013) Division of labor during primary humoral immunity. Immunol Res 55:277-86|
|Rowland, Sarah L; Tuttle, Kathryn; Torres, Raul M et al. (2013) Antigen and cytokine receptor signals guide the development of the naive mature B cell repertoire. Immunol Res 55:231-40|
|Saumyaa; Arjunaraja, Swadhinya; Pujanauski, Lindsey et al. (2013) Immunosuppressive property within the Streptococcus pneumoniae cell wall that inhibits generation of T follicular helper, germinal center, and plasma cell response to a coimmunized heterologous protein. Infect Immun 81:3426-33|
|Pujanauski, Lindsey M; Janoff, Edward N; McCarter, Martin D et al. (2013) Mouse marginal zone B cells harbor specificities similar to human broadly neutralizing HIV antibodies. Proc Natl Acad Sci U S A 110:1422-7|
|Oda, Shannon K; Strauch, Pamela; Fujiwara, Yuko et al. (2013) Lysophosphatidic acid inhibits CD8 T cell activation and control of tumor progression. Cancer Immunol Res 1:245-55|
|Larson, Jennifer D; Thurman, Joshua M; Rubtsov, Anatoly V et al. (2012) Murine gammaherpesvirus 68 infection protects lupus-prone mice from the development of autoimmunity. Proc Natl Acad Sci U S A 109:E1092-100|
|Teodorovic, Lenka Sinik; Riccardi, Carlo; Torres, Raul M et al. (2012) Murine B cell development and antibody responses to model antigens are not impaired in the absence of the TNF receptor GITR. PLoS One 7:e31632|
|Fournier, Emilie M; Velez, Maria-Gabriela; Leahy, Katelyn et al. (2012) Dual-reactive B cells are autoreactive and highly enriched in the plasmablast and memory B cell subsets of autoimmune mice. J Exp Med 209:1797-812|
|Pelanda, Roberta; Torres, Raul M (2012) Central B-cell tolerance: where selection begins. Cold Spring Harb Perspect Biol 4:a007146|
Showing the most recent 10 out of 22 publications