Figure 3
Figure 3. Absence of B cells in the secondary lymphoid tissues and impaired B-cell development in the bone marrow of Pbx1−/−Rag1−/− chimeric mice. (A) FACS analysis was performed on cells harvested from the spleen, lymph node, and peritoneal cavity of chimeric mice. Staining with anti-B220 (B cells) and anti-Ly9.1 (donor) antibodies showed that all sites in Pbx1−/−Rag1−/− mice were devoid of donor-derived B cells (Ly9.1+B220+). (B) Hardy profile analysis25 was performed on bone marrow cells of chimeric mice. Donor-derived (Ly9.1+) cells from fractions A through C (B220+CD43+) and D through F (B220+CD43−) were completely absent in the bone marrow of the Pbx1−/−Rag1−/− mice. (C) FACS analysis of bone marrow cells for CLPs19 revealed the absence of Ly9.1+ CLPs in Pbx1−/−Rag1−/− chimeras. (D) FACS analysis of bone marrow cells for HSCd revealed the presence of Ly9.1+ HSCs in Pbx1−/−Rag1−/− chimeras.

Absence of B cells in the secondary lymphoid tissues and impaired B-cell development in the bone marrow of Pbx1−/−Rag1−/− chimeric mice. (A) FACS analysis was performed on cells harvested from the spleen, lymph node, and peritoneal cavity of chimeric mice. Staining with anti-B220 (B cells) and anti-Ly9.1 (donor) antibodies showed that all sites in Pbx1−/−Rag1−/− mice were devoid of donor-derived B cells (Ly9.1+B220+). (B) Hardy profile analysis25  was performed on bone marrow cells of chimeric mice. Donor-derived (Ly9.1+) cells from fractions A through C (B220+CD43+) and D through F (B220+CD43) were completely absent in the bone marrow of the Pbx1−/−Rag1−/− mice. (C) FACS analysis of bone marrow cells for CLPs19  revealed the absence of Ly9.1+ CLPs in Pbx1−/−Rag1−/− chimeras. (D) FACS analysis of bone marrow cells for HSCd revealed the presence of Ly9.1+ HSCs in Pbx1−/−Rag1−/− chimeras.

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