ABSTRACT
The amplitude and duration of Ca2+ signaling is crucial for B-cell development and self-tolerance; however, the mechanisms for terminating Ca2+ signals in B cells have not been determined. In lymphocytes, plasma membrane Ca2+ ATPase (PMCA) isoforms 1 and 4 (PMCA1 and PMCA4, aka ATP2B1 and ATP2B4) are the main candidates for expelling Ca2+ from the cell through the plasma membrane. We report here that Pmca4 (Atp2b4) KO mice had normal B-cell development, while mice with a conditional KO of Pmca1 (Atp2b1) had greatly reduced numbers of B cells, particularly splenic follicular B cells, marginal zone B cells, and peritoneal B-1a cells. Mouse and naïve human B cells showed only PMCA1 expression and no PMCA4 by western blot, in contrast to T cells, which did express PMCA4. Calcium handling was normal in Pmca4-/- B cells, but Pmca1 KO B cells had elevated basal levels of Ca2+ , elevated levels in ER stores, and reduced Ca2+ clearance. These findings show that the PMCA1 isoform alone is required to ensure normal B-cell Ca2+ signaling and development, which may have implications for therapeutic targeting of PMCAs and Ca2+ in B cells.
Subject(s)
B-Lymphocytes/metabolism , Calcium-Transporting ATPases/metabolism , Calcium/metabolism , Cell Membrane/metabolism , Homeostasis/physiology , Plasma Membrane Calcium-Transporting ATPases/metabolism , Animals , Mice , Mice, Inbred C57BL , Mice, Knockout , Protein Isoforms/metabolism , Signal Transduction/physiologyABSTRACT
Marginal zone B cells (MZBs) are a population of B cells that reside in the mouse splenic marginal zones that envelop follicles. To reach the follicles, MZBs must migrate up the shear force of blood flow. We present here a method for analyzing this flow-induced MZB migration in vitro. First, MZBs are isolated from the mouse spleen. Second, MZBs are settled on integrin ligands in flow chamber slides, exposed to shear flow, and imaged under a microscope while migrating. Third, images of the migrating MZBs are processed using the MTrack2 automatic cell tracking plugin for ImageJ, and the resulting cell tracks are quantified using the Ibidi chemotaxis tool. The migration data reveal how fast the cells move, how often they change direction, whether the shear flow vector affects their migration direction, and which integrin ligands are involved. Although we use MZBs, the method can easily be adapted for analyzing migration of any leukocyte that responds to the force of shear flow.
Subject(s)
B-Lymphocytes/physiology , Cell Movement/physiology , Chemotaxis/physiology , Time-Lapse Imaging/methods , Animals , B-Lymphocytes/chemistry , Cells, Cultured , Lymphoid Tissue/chemistry , Lymphoid Tissue/cytology , Lymphoid Tissue/physiology , Mice , Spleen/chemistry , Spleen/cytology , Spleen/physiologyABSTRACT
Germinal centers (GCs) are the sites where B cells undergo affinity maturation. The regulation of cellular output from the GC is not well understood. Here, we show that from the earliest stages of the GC response, plasmablasts emerge at the GC-T zone interface (GTI). We define two main factors that regulate this process: Tfh-derived IL-21, which supports production of plasmablasts from the GC, and TNFSF13 (APRIL), which is produced by a population of podoplanin+ CD157high fibroblastic reticular cells located in the GTI that are also rich in message for IL-6 and chemokines CXCL12, CCL19, and CCL21. Plasmablasts in the GTI express the APRIL receptor TNFRSF13B (TACI), and blocking TACI interactions specifically reduces the numbers of plasmablasts appearing in the GTI. Plasma cells generated in the GTI may provide an early source of affinity-matured antibodies that may neutralize pathogens or provide feedback regulating GC B cell selection.
Subject(s)
Germinal Center/cytology , Plasma Cells/metabolism , Signal Transduction , Stromal Cells/cytology , T-Lymphocytes, Helper-Inducer/cytology , Animals , Antigens/metabolism , Cell Differentiation , Cell Movement , Chemokines/metabolism , Gene Expression Regulation , Immunity , Interferon Regulatory Factors/metabolism , Interleukins/genetics , Interleukins/metabolism , Ligands , Lymphocyte Activation/immunology , Mice, Inbred C57BL , RNA, Messenger/genetics , RNA, Messenger/metabolism , Stromal Cells/metabolism , T-Lymphocytes, Helper-Inducer/metabolism , Transmembrane Activator and CAML Interactor Protein/metabolism , Tumor Necrosis Factor Ligand Superfamily Member 13/genetics , Tumor Necrosis Factor Ligand Superfamily Member 13/metabolismABSTRACT
Splenic marginal zone B cells (MZB) shuttle between the blood-filled marginal zone for antigen collection and the follicle for antigen delivery. However, it is unclear how MZBs migrate directionally from the marginal zone to the follicle. Here, we show that murine MZBs migrate up shear flow via the LFA-1 (αLß2) integrin ligand ICAM-1, but adhere or migrate down the flow via the VLA-4 integrin (α4ß1) ligand VCAM-1. MZBs lacking Arhgef6 (Pak-interacting exchange factor (αPIX)) or functional LFA-1 are impaired in shuttling due to mislocalization toward the VCAM-1-rich red pulp. Sphingosine-1-phosphate (S1P) signaling through the S1PR3 receptor inhibits MZB migration up the flow, and deletion of S1pr3 in Arhgef6 -/- mice rescues mislocalized MZBs. These findings establish shear flow as a directional cue for MZB migration to the follicle, and define S1PR3 and VCAM-1 as counteracting forces that inhibit this migration.
Subject(s)
B-Lymphocytes/physiology , Cell Movement/physiology , Intercellular Adhesion Molecule-1/metabolism , Lysophospholipids/metabolism , Receptors, Lysosphingolipid/genetics , Sphingosine/analogs & derivatives , Stress, Mechanical , Vascular Cell Adhesion Molecule-1/metabolism , Animals , B-Lymphocytes/metabolism , Integrin alpha4beta1/metabolism , Lymphocyte Function-Associated Antigen-1/metabolism , Mice , Mice, Knockout , Receptors, Lysosphingolipid/metabolism , Regional Blood Flow , Rho Guanine Nucleotide Exchange Factors/genetics , Signal Transduction , Sphingosine/metabolism , Sphingosine-1-Phosphate Receptors , Spleen/cytologyABSTRACT
Due to the multitude of cell types involved in the differentiation of plasma cells during the germinal center reaction, and due to a lack of in vitro systems, which recapitulate germinal centers, the most suitable way to study plasma cell generation in germinal centers is in vivo. In this chapter we describe how to induce humoral immune responses to defined model antigens and how to visualize and track plasma cells and their interactions with other cells in the lymph nodes of living mice.
