Figure 1
Figure 1. Canonical early DC progenitors are absent from the adult thymus. (A) BM (upper panel) and thymic (lower panel) cells from CX3CR1GFP/+ reporter mice were labeled with antibodies against lineage markers (CD19, TCR-β, NK1.1, CD11b, and Gr-1), along with CD11c, MHC-II, and CD135 and analyzed by FACS to detect pre-DCs (CD11c+MHC-II−). Representative FACS density plots indicate the pre-DC population in the BM and thymus. Numbers next to gates indicate the percentage of cells. (B) Similar to (A), the BM and thymic cells from CX3CR1GFP/+ reporter mice were stained with lineage markers (CD19, TCR-β, NK1.1, CD11b, CD11c, and Gr-1), as well as Sca-1, CD135, CD117, and CD115 antibodies to visualize MPs (Lin−Sca-1−CD117hiCD135+CX3CR1−), MDPs (CD117hiCD135+CX3CR1+), and CDPs (CD117+CD135+CX3CR1+CD115+) in the BM (upper panel) and thymus (lower panel). Representative FACS density plots indicate frequencies of MP, MDP, and CDP. Results are representative of 3 independent experiments with at least 3 mice per group.

Canonical early DC progenitors are absent from the adult thymus. (A) BM (upper panel) and thymic (lower panel) cells from CX3CR1GFP/+ reporter mice were labeled with antibodies against lineage markers (CD19, TCR-β, NK1.1, CD11b, and Gr-1), along with CD11c, MHC-II, and CD135 and analyzed by FACS to detect pre-DCs (CD11c+MHC-II). Representative FACS density plots indicate the pre-DC population in the BM and thymus. Numbers next to gates indicate the percentage of cells. (B) Similar to (A), the BM and thymic cells from CX3CR1GFP/+ reporter mice were stained with lineage markers (CD19, TCR-β, NK1.1, CD11b, CD11c, and Gr-1), as well as Sca-1, CD135, CD117, and CD115 antibodies to visualize MPs (LinSca-1CD117hiCD135+CX3CR1), MDPs (CD117hiCD135+CX3CR1+), and CDPs (CD117+CD135+CX3CR1+CD115+) in the BM (upper panel) and thymus (lower panel). Representative FACS density plots indicate frequencies of MP, MDP, and CDP. Results are representative of 3 independent experiments with at least 3 mice per group.

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