Author/Authors :
Buchanan، نويسنده , , Rachelle M. and Popowych، نويسنده , , Yurij and Arsic، نويسنده , , Natasha and Townsend، نويسنده , , Hugh G.G. and Mutwiri، نويسنده , , George K. and Potter، نويسنده , , Andrew A. and Babiuk، نويسنده , , Lorne A. and Griebel، نويسنده , , Philip J. and Wilson، نويسنده , , Heather L.، نويسنده ,
Abstract :
It is controversial whether naïve B cells are directly activated in response to TLR9 ligand, CpG ODN. Although bovine blood-derived CD21+ B cells express TLR9 and proliferate in response to CpG in mixed-cell populations, purified bovine B cells do not proliferate significantly in response to CpG ODN, even when the B cell receptor is engaged. When co-cultured with CD14+ myeloid cells and/or B-cell activating factor (BAFF), a cytokine produced by activated myeloid cells, there was a significant increase in CpG-specific B cell proliferation, and the number of large B cells in general or positive for CD25, all of which are markers for B cell activation. These data suggest that activated myeloid cells and BAFF prime B cells for significant CpG-specific activation. Understanding the signals required to mediate efficient CpG-induced, antigen-independent and T-cell independent activation of B cells has implications for polyclonal B cell activation and the development of autoimmune diseases.
Keywords :
B cell , BAFF , Naive , Bovine , Myeloid cells , TLR9