Anti-CD180 (RP105) Activates B Cells To Rapidly Produce Polyclonal Ig via a T Cell and MyD88-Independent Pathway
Autor: | Jeffrey A. Ledbetter, Jay W. Chaplin, Shinji Kasahara, Edward A. Clark |
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Rok vydání: | 2011 |
Předmět: |
T-Lymphocytes
T cell Immunology Naive B cell Immunoglobulins Enzyme-Linked Immunosorbent Assay Cell Separation Lymphocyte Activation Article Mice Antigens CD Marginal zone B-cell medicine Animals Immunology and Allergy Follicular B cell B cell Cell Proliferation Mice Knockout CD86 B-Lymphocytes CD40 biology Cell Differentiation hemic and immune systems Flow Cytometry Molecular biology Mice Inbred C57BL medicine.anatomical_structure Antibody Formation Myeloid Differentiation Factor 88 biology.protein CD80 |
Zdroj: | The Journal of Immunology. 187:4199-4209 |
ISSN: | 1550-6606 0022-1767 |
DOI: | 10.4049/jimmunol.1100198 |
Popis: | CD180 is homologous to TLR4 and regulates TLR4 signaling, yet its function is unclear. We report that injection of anti-CD180 mAb into mice induced rapid Ig production of all classes and subclasses, with the exception of IgA and IgG2b, with up to 50-fold increases in serum IgG1 and IgG3. IgG production after anti-CD180 injection was not due to reactivation of memory B cells and was retained in T cell-deficient (TCR knockout [KO]), CD40 KO, IL-4 KO, and MyD88 KO mice. Anti-CD180 rapidly increased both transitional and mature B cells, with especially robust increases in transitional B cell number, marginal zone B cell proliferation, and CD86, but not CD80, expression. In contrast, anti-CD40 induced primarily follicular B cell and myeloid expansion, with increases in expression of CD80 and CD95 but not CD86. The expansion of splenic B cells was due, in part, to proliferation and occurred in wild-type and TCR KO mice, whereas T cell expansion occurred in wild-type, but not in B cell-deficient, mice, indicating a direct role for B cells in CD180 stimulation in vivo. Combination of anti-CD180 with various MyD88-dependent TLR ligands biased B cell fate because coinjection diminished Ig production, but purified B cells exhibited synergistic proliferation. Anti-CD180 had no effect on cytokine production from B cells, but it increased IL-6, IL-10, and TNF-α production in combination with LPS or CpG. Thus, CD180 stimulation induces intrinsic B cell proliferation and differentiation, causing rapid increases in IgG, and integrates MyD88-dependent TLR signals to regulate proliferation, cytokine production, and differentiation. |
Databáze: | OpenAIRE |
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