Figure 4.
TLR1/2 agonist treatment is associated with decreased bone marrow SECs. Wild-type mice were treated with PAM3CSK4 (100 μg, every other day × 3 doses) and analyzed 24 hours after the final dose. (A) Representative images of femur sections stained for vascular endothelial–cadherin (VE-cad; red) and 4′,6-diamidino-2-phenylindole (DAPI; blue). (B) Quantification of the VE-cad signal by histomorphometry. (C) Representative flow plots showing gating strategy to identify CD31+ Sca1– CD45– Ter119– SECs and CD31+ Sca1+ CD45– Ter119– AECs. Quantification of SECs (D) and AECs (E). Data represent the mean ± standard error of the mean. Statistical significance determined by using an unpaired t-test. ∗P < .05, ∗∗P < .01.

TLR1/2 agonist treatment is associated with decreased bone marrow SECs. Wild-type mice were treated with PAM3CSK4 (100 μg, every other day × 3 doses) and analyzed 24 hours after the final dose. (A) Representative images of femur sections stained for vascular endothelial–cadherin (VE-cad; red) and 4′,6-diamidino-2-phenylindole (DAPI; blue). (B) Quantification of the VE-cad signal by histomorphometry. (C) Representative flow plots showing gating strategy to identify CD31+ Sca1 CD45 Ter119 SECs and CD31+ Sca1+ CD45 Ter119 AECs. Quantification of SECs (D) and AECs (E). Data represent the mean ± standard error of the mean. Statistical significance determined by using an unpaired t-test. ∗P < .05, ∗∗P < .01.

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