TY - JOUR
T1 - Fetal reversion from diverse lineages sustains the intestinal stem cell pool and confers stress resilience
AU - Kirino, Sakura
AU - Uefune, Fumiya
AU - Miyake, Kensuke
AU - Ogasawara, Nobuhiko
AU - Kobayashi, Sakurako
AU - Watanabe, Satoshi
AU - Hiraguri, Yui
AU - Ito, Go
AU - Akahoshi, Keiichi
AU - Ban, Daisuke
AU - van Es, Johan H.
AU - Clevers, Hans
AU - Watanabe, Mamoru
AU - Okamoto, Ryuichi
AU - Yui, Shiro
N1 - © 2026. The Author(s).
PY - 2026/1/13
Y1 - 2026/1/13
N2 - Plasticity is a central mechanism underlying the robust regenerative capacity of the intestinal epithelium. Two major forms of plasticity have been described: spatial plasticity, in which differentiated cells revert to crypt base columnar cells (CBCs), and fetal reversion into revival stem cells (revSCs). However, the relationship among these two stem cell populations and differentiated cells remains to be clarified. Here, we demonstrated the bidirectional interconversion between CBCs and revSCs. Using lineage tracing, injury models and villus culture, we show that absorptive enterocytes can reprogram into revSCs and regenerate CBCs. These findings position fetal reversion as an entry point to spatial plasticity, establishing a regenerative hierarchy where CBCs, revSCs, and enterocytes collectively orchestrate intestinal repair. Furthermore, we identified revSCs as a highly stress-tolerant stem cell population, whose emergence would preserve the stem cell pool. Our results establish fetal reversion as a cellular escape mechanism safeguarding epithelial regeneration under inflammatory conditions.
AB - Plasticity is a central mechanism underlying the robust regenerative capacity of the intestinal epithelium. Two major forms of plasticity have been described: spatial plasticity, in which differentiated cells revert to crypt base columnar cells (CBCs), and fetal reversion into revival stem cells (revSCs). However, the relationship among these two stem cell populations and differentiated cells remains to be clarified. Here, we demonstrated the bidirectional interconversion between CBCs and revSCs. Using lineage tracing, injury models and villus culture, we show that absorptive enterocytes can reprogram into revSCs and regenerate CBCs. These findings position fetal reversion as an entry point to spatial plasticity, establishing a regenerative hierarchy where CBCs, revSCs, and enterocytes collectively orchestrate intestinal repair. Furthermore, we identified revSCs as a highly stress-tolerant stem cell population, whose emergence would preserve the stem cell pool. Our results establish fetal reversion as a cellular escape mechanism safeguarding epithelial regeneration under inflammatory conditions.
KW - Cell Lineage
KW - Intestinal Mucosa/cytology
KW - Regeneration
KW - Animals
KW - Stress, Physiological
KW - Cell Differentiation
KW - Mice
KW - Enterocytes/cytology
KW - Stem Cells/cytology
UR - https://www.scopus.com/pages/publications/105030164694
UR - https://www.mendeley.com/catalogue/d91c108a-2431-3a67-82fe-ede5a430b17a/
U2 - 10.1038/s42003-026-09533-x
DO - 10.1038/s42003-026-09533-x
M3 - Article
C2 - 41530496
AN - SCOPUS:105030164694
SN - 2399-3642
VL - 9
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 255
ER -