Figure 5
Figure 5. CD11c-specific depletion of p14 inhibits mitosis of LCs. (A-B) Quantification of total and mitotic LCs of 7-day-old CD11c-p14del and control mice. LCs are stained for MHC II (red fluorescence) and phospho-Histone H3 (green fluorescence). Fifteen pictures of randomly chosen areas were recorded and the total number of LCs per mm2, as well as the proportions of mitotic LCs (arrowheads), were quantified. Combined data from 3 to 4 mice per genotype are depicted in panel B. Scale bar: 20 µm. (C) Staining patterns of phospho-Histone H3 allow identification of mitotic phases: late G2 or prophase, metaphase, and telophase/cytokinesis. All stages of mitotic LCs were found both in CD11c-p14del and in control mice. Examples shown here are from control mice. (D-E) LC cell-cycle distribution based on BrdU/7AAD incorporation on day 8 after birth. MHC II+ LCs and CD3+ DETCs were analyzed for intercalation of BrdU and 7AAD and further divided into 3 cell-cycle phases: G1/G0: BrdUneg7AADlow; S: BrdU+7AADlow-high; G2/M: BrdUneg7AADhigh. One representative experiment of an 8-day-old neonatal mouse in panel D (n = 5); combined data from 8 individually analyzed mice per genotype in panel E. **P < .01, ***P < .001.

CD11c-specific depletion of p14 inhibits mitosis of LCs. (A-B) Quantification of total and mitotic LCs of 7-day-old CD11c-p14del and control mice. LCs are stained for MHC II (red fluorescence) and phospho-Histone H3 (green fluorescence). Fifteen pictures of randomly chosen areas were recorded and the total number of LCs per mm2, as well as the proportions of mitotic LCs (arrowheads), were quantified. Combined data from 3 to 4 mice per genotype are depicted in panel B. Scale bar: 20 µm. (C) Staining patterns of phospho-Histone H3 allow identification of mitotic phases: late G2 or prophase, metaphase, and telophase/cytokinesis. All stages of mitotic LCs were found both in CD11c-p14del and in control mice. Examples shown here are from control mice. (D-E) LC cell-cycle distribution based on BrdU/7AAD incorporation on day 8 after birth. MHC II+ LCs and CD3+ DETCs were analyzed for intercalation of BrdU and 7AAD and further divided into 3 cell-cycle phases: G1/G0: BrdUneg7AADlow; S: BrdU+7AADlow-high; G2/M: BrdUneg7AADhigh. One representative experiment of an 8-day-old neonatal mouse in panel D (n = 5); combined data from 8 individually analyzed mice per genotype in panel E. **P < .01, ***P < .001.

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