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. Author manuscript; available in PMC: 2021 Nov 26.
Published in final edited form as: Nat Immunol. 2021 May 26;22(6):699–710. doi: 10.1038/s41590-021-00934-0

Extended Data Fig. 2.

Extended Data Fig. 2

Diphtheria toxin (DT) administered every two days from day 8 to 14 (DT8–14) after birth followed by quantitative analyses on day 15 (H15) of the absolute count of macrophages (CD45+ Lin F4/80+ CD64+) in the skin (LysCre+/−: n=3, MMDTR n=4) (A) or spleen (LysCre+/−: n=5, MMDTR n=5) (B) and the absolute count of iNKT (CD45+ CD3ε+ TCRβ+ CD1d Tetramer+) and TCR-αβ+ T (CD45+ CD3ε+ TCRβ+) cells in the skin (LysCre+/−: n=8, MMDTR n=7) (C) of control littermates LysCre+/− or MMDTR animals. DT administered from day 8 to 10 (DT8–10) after birth followed by quantitative analyses on day 11 (H11) of the absolute count of iNKT and TCR-αβ+ T cells in the small intestine (D) and lung (E) of control littermates LysCre+/− (n=3) or MMDTR (n=12) animals. DT administered from day 8 to 10 (DT8–10) after birth followed by quantitative analyses on day 11 (H11) of the absolute count of splenic macrophages (F) of control littermates LysCre+/− (n=5) or MMDTR (n=3) animals. DT administered from day 12 to 14 (DT12–14) after birth followed by quantitative analyses on day 15 (H15) of the absolute count of splenic macrophages (G) of control littermates LysCre+/− (n=9) or MMDTR (n=10) animals. Absolute counts were determined by flow cytometry. Error bars indicate standard error of mean. Each dot is representative of an individual mouse. P values were calculated by unpaired two-sided Student’s t-test. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.0001.