2B bottom and data not shown), i.e. have the same phenotype of B-1 cells in the spleen (Supporting Information Fig. 1). Importantly, these spontaneous natural IgM-secreting cells are thus distinct from a recently described BM IgMloIgDhi B cell subset that is induced following T-independent responses to blood-borne pathogens to secrete IgM 42. Our phenotype-based functional analysis strongly suggested the presence of spontaneous IgM secreting B-1 cells in the BM. To confirm this, we generated Ig-allotype chimeric mice that harbor B-1 and B-2 cells of different allotypes, Igh-a and Igh-b respectively

25, 26, 43, 44. Using Ig-allotype BIBW2992 mouse and isotype-specific monoclonal antibodies, even low frequencies of B-1 (Igh-a) cells can be identified in these chimeras without having to rely on surface markers that might change upon activation

and/or differentiation of B-1 cells. Flow cytometric analysis of these mice demonstrated the presence of B-1 cells in PerC, spleen and the BM (Fig. 3A). BM B-1 cells (Igh-a) were CD19hiCD43+, i.e. identical to the population of spontaneous IgM-secreting cells in BALB/c mouse BM (Fig. 3A and Fig. 2B). Comparative analysis of B-1 cells in PerC, spleen and BM showed similar phenotypic profiles of splenic and BM B-1 cells and consistent differences of https://www.selleckchem.com/products/DAPT-GSI-IX.html these two populations compared with PerC B-1 cells. Spleen and BM B-1 cells were larger compared with resting B-2 cells but smaller than B-1 cells in the PerC. CD43 was expressed homogeneously on B-1 cells in BM Plasmin and spleen (Fig. 3B) and CD11b was not expressed by

these cells (25 and data not shown). In contrast, PerC B-1 cells showed a bimodal expression pattern of CD43 and most expressed CD11b (Fig. 3B and data not shown). B-2 cells lacked both markers completely, at least in steady state (25, 30, 45 and Fig. 3B). Independent of their tissue location, all B-1 cells expressed higher levels of CD19 than B-2 cells and B-1 cells in all tissues were heterogeneous with regard to surface expression of CD5 (Fig. 3B), with the majority (> 80%) expressing measurable levels of CD5. B-1 (Igh-a) cell frequencies in the BM were about 6-fold lower compared with those found in the spleen (0.44±0.13% and 2.33±0.58% among live cells respectively) and >100-fold lower than in the peritoneal cavity (Fig. 3C). We identified similar frequencies of IgM+CD43+CD5+/− B cells in the BM of BALB/c mice (Supporting Information Fig.1). Given the total number of BM cells received per femur (mean of 4.59×107/cells per BALB/c mouse; n=8) and a calculated number of total BM cells (one femur =12.7% of total BM cells 46, i.e. 3.61×108/mouse), we can calculate the total number of BM B-1 cells to be roughly 1.6×106/mouse. A very similar number is found in the spleen: 1.8×106 (mean of 7.74×107 total cells/mouse; n = 9; and 2.33% B-1 cells) and half of the number found in the peritoneal cavity: 3.

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