Bcl6 can efficiently repress the expression of Blimp-1 and subsequent plasma cell differentiation ([8, 54, 61, 62], J. Alinikula, K.-P. Nera, S. Junttila and O. Lassila, unpublished

observations). The repression can occur directly by interfering with the function of Blimp-1-inducing STAT3 [62] and independently by binding to Blimp-1 intronic sequences [61, 63]. Additionally, Bcl6 may repress Blimp-1 via regulating the other repressors of Blimp-1, such as Bach2 (J. Alinikula, K.-P. Nera, S. Junttila and O. Lassila unpublished observations). Thus, the function of Bcl6 is to prevent the SAR245409 cell line premature differentiation of plasma cells to allow effective Ig SHM and CSR during the GC response (Fig. 3). In addition to inducing the activators of plasma cell differentiation, the repressors of plasma cell differentiation Pax5, MITF, Bach2 and Bcl6 [8, 28, 61, 62, 64, 65] need to be suppressed (Fig. 3). The downregulation of Pax5, a central factor for the commitment and maintenance of B cell phenotype [66], is crucial for the plasma cell differentiation [9]. Pax5 expression can efficiently prevent the differentiation of antibody-secreting plasma cells and the expression of Blimp-1 [9, 28, 67–69]. Pax5 also represses

the expression of Selleckchem AZD1152HQPA several genes associated with immunoglobulin secretion, such as Ig J-chain [70–72] and Xbp1 [8, 9, 35], and inhibits high-level transcription of Ig loci [73]. Inactivation of Pax5 gene in DT40 B cells induces plasma cell transcription programme and Ig secretion [8]. Conditional inactivation of Pax5 in mature B cells induces also a similar phenotype [28]. The downregulation of Pax5 is one of the initiating mechanisms of plasma cell differentiation in GCs. The evidence for this

comes from the experiments where Blimp-1 gene was engineered to harbour a GFP reporter gene [20]. This model was used to discover a population of GC cells called preplasmablasts that have downregulated the expression of Pax5 but not yet induced the expression of Blimp-1 [27] suggesting that B cell properties Oxalosuccinic acid are not lost only after the induction of Blimp-1 but rather precede the Blimp-1 expression. Pax5 can also directly repress the Blimp-1 expression [67]. In line with these results, inactivation of Pax5 in DT40 cells leads to spontaneous differentiation to plasma cells [8]. The mechanism for physiological suppression of Pax5 expression in GCs is however currently unknown. The Pax5-deficient DT40 cells have, however, also lost their Bcl6 expression [8] warranting the possibility that Pax5 deletion induces plasma cell differentiation via upregulation of Blimp-1 after losing Bcl6-mediated Blimp-1 repression. Indeed, Bcl6 expression in Pax5 deficient cells can repress Blimp-1 [8], but not vice versa: enforced Pax5 expression in Bcl6-deficient cells cannot repress Blimp-1 (J. Alinikula, K.-P. Nera, S. Junttila and O.