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. 2017 Dec 7;10(1):27–42. doi: 10.1016/j.stemcr.2017.11.006

Figure 4.

Figure 4

Formation of ATOH1+ IEC-Derived Clonal Ribbon Is Significantly Promoted during Regeneration from Colitis-Induced Epithelial Damage

Formation of ATOH1+ IEC-derived clonal ribbon (ATOH1+ICR) was compared between the DSS-colitis mice (DSS) and control mice (Control).

(A) Experimental design for the lineage-tracing analysis of Atoh1+ IECs in DSS-colitis-induced Atoh1tdTomato mice.

(B) Labeling of ATOH1+ IECs-derived cells by tdTomato (red) at day 6 in the colon of DSS-colitis mice and control mice.

(C) Double RNAscope ISH showing expression of Atoh1 (red) and Lgr5 (green) in the colonic crypts of DSS-colitis mice and control mice. Magnified view of the designated area (white square) is shown in the right end column. Images of the colon are re-used in Figure 2C.

(D) An example of ATOH1+ICR forming the wound-associated epithelium in DSS-colitis mouse on day 13.

(E) Representative rectal sections showing ATOH1+ICRs (red) in the control mice (Control) and in the DSS-colitis mice (DSS) on day 20.

(F) Quantification of the ATOH1+ICR formation frequency in the rectum of DSS-colitis mice (n = 3) and control mice (n = 3). The number of ATOH1+ICR was normalized by the total number of crypts. Data are expressed as the mean ± SEM per 1,000 crypts. p < 0.0001.

See also Figure S4.