Skip to main content
. 2021 Feb 27;12(1):251–276. doi: 10.1016/j.jcmgh.2021.02.008

Figure 4.

Figure 4

Proportion of main immune cells in peripheral organs of CJ mice, Bmal1-/-mice, and Per1-/-Per2-/-mice. (A–D) Proportion of B220+ cells, CD3+ cells, CD11c+ cells, CD49b+ cells, and CD11b+ cells in peripheral organs of CJ mice, Bmal1-/- mice, and Per1-/-Per2-/- mice. (E–H) Proportion of subpopulations of B cells in peripheral organs of CJ mice, Bmal1-/- mice, and Per1-/-Per2-/- mice. (I) Fluorescence-activated cell sorter (FACS) graphs showing B220+CD1d+CD5+ cells, MFI of IL10 and IL33 on B220+CD1d+CD5+ cells in IELs from DSS-treated or untreated Bmal1-/- and WT mice. (J) Proportion of CD1d+CD5+cells of B220+ cells in IELs. (K) MFI of IL33 and (L) IL10 on B220+CD1d+CD5+ in IELs. (M) Rhythmic oscillation of proportion of B220+CD1d+CD5+ cells in the IELs and (N) hepatic lymphocytes from DSS-treated Bmal1-/- and WT mice within 24 hours. The P value is estimated by JTK cycle analysis. FSC, forward scatter; NC, non-specific control; PE, Phycoerythrin; SSC, side scatter.