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. 2024 Jan 23;65(2):194–204. doi: 10.1093/jrr/rrad104

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© The Author(s) 2024. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 2 — Histopathological analysis on mouse intestinal epithelium after TAI. (A) HE staining revealing the mitigation of ^T7E21RHD5 on the intestinal mucosal destruction caused by IR. Scale indicates 200 μm. (B) Counts of mouse ileal villous height. Results are shown as means ± SD. ^***P < 0.001. (C) Number of crypts in mouse ileum in the presence and absence of TAI and peptide treatment. Results are shown as means ± SD. ^***P < 0.001. (D) PAS staining showing goblet cells in mouse ileum. Scale indicates 200 μm. (E) Counts of goblet cells in mouse ileum after TAI and peptide treatment. Results are shown as means ± SD. ^***P < 0.001.