Abstract: |
Radiation causes intestinal injury, as occurs in abdominal and pelvic tumor radiotherapy. Intestinal stem cells (ISCs) are critical for epithelial regeneration. In this article, Hua and colleagues show that Bach2 deficiency promotes intestinal epithelial regeneration by accelerating DNA repair in ISCs, resulting in a reduction in mortality during radiation-induced intestine injury. © 2020 The Authors Epithelial regeneration is critical for barrier maintenance and organ function after intestinal injury, although the repair mechanisms are unclear. Here, we found that Bach2 deficiency promotes intestinal epithelial cell proliferation during homeostasis. Moreover, genetic inactivation of Bach2 in mouse intestinal epithelium facilitated crypt regeneration after irradiation, resulting in a reduction in mortality. RNA-sequencing analysis of isolated crypts revealed that Bach2 deficiency altered the expression of numerous genes, including those regulating double-strand break repair. Mechanistic characterizations indicated that Bach2 deletion facilitated DNA repair in intestinal crypt cells, as evidenced by faster resolution of γ-H2AX and 53BP1 foci in Bach2−/− crypt cells, compared with Bach2+/+ control. Together, our studies highlight that Bach2 deficiency promotes intestinal regeneration by accelerating DNA repair in intestinal stem cells after radiation damage. © 2020 The Authors |