Figure 3
Figure 3. Accumulation of MZ B cells in p100−/− mice is cell intrinsic. (A) Lethally irradiated C57BL/6 recipients were reconstituted with either wild-type (wt → B6) or p100−/− bone marrow cells (p100−/− → B6). At 6 weeks after transplantation, splenocytes from chimeras were stained for CD23, CD21, and IgM and analyzed for MZ B cells (CD23−CD21hiIgMhi). Only CD23− lymphocytes are shown. (B) MZ B-cell accumulation in p100−/− mice is dependent on relB. Splenocytes from wild-type, p100−/−relB−/+, and p100−/−relB−/− mice were analyzed for MZ B cells as described in panel A.

Accumulation of MZ B cells in p100−/− mice is cell intrinsic. (A) Lethally irradiated C57BL/6 recipients were reconstituted with either wild-type (wtB6) or p100−/− bone marrow cells (p100−/−B6). At 6 weeks after transplantation, splenocytes from chimeras were stained for CD23, CD21, and IgM and analyzed for MZ B cells (CD23CD21hiIgMhi). Only CD23 lymphocytes are shown. (B) MZ B-cell accumulation in p100−/− mice is dependent on relB. Splenocytes from wild-type, p100−/−relB−/+, and p100−/−relB−/− mice were analyzed for MZ B cells as described in panel A.

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