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Publication : LIF is essential for ISC function and protects against radiation-induced gastrointestinal syndrome.

First Author  Wang H Year  2020
Journal  Cell Death Dis Volume  11
Issue  7 Pages  588
PubMed ID  32719388 Mgi Jnum  J:305498
Mgi Id  MGI:6705830 Doi  10.1038/s41419-020-02790-6
Citation  Wang H, et al. (2020) LIF is essential for ISC function and protects against radiation-induced gastrointestinal syndrome. Cell Death Dis 11(7):588
abstractText  Leukemia inhibitory factor (LIF) is a cytokine essential for maintaining pluripotency of mouse embryonic stem cells. However, its role in adult intestinal stem cells (ISCs) is unclear. The adult intestinal epithelium has a high self-renewal rate driven by ISCs in crypts. Here, we find that LIF is present in the ISC niche in crypts and critical for the function of ISCs in maintaining the intestinal epithelial homeostasis and regeneration. Mechanistically, LIF maintains beta-catenin activity through the AKT/GSK3beta signaling to regulate ISC functions. LIF deficiency in mice impairs the renewal of the intestinal epithelium under the physiological condition. Further, LIF deficiency in mice impairs the regeneration of intestinal epithelium in response to radiation and shortens the lifespan of mice after high doses of radiation due to gastrointestinal (GI) syndrome, which can be rescued by administering recombinant LIF (rLIF). Importantly, LIF exhibits a radioprotective role in wild-type (WT) mice by protecting mice from lethal radiation-induced GI syndrome; administering rLIF promotes intestinal epithelial regeneration and prolongs survival in WT mice after radiation. These results reveal a previously unidentified and a crucial role of LIF in ensuring ISC function, promoting regeneration of the intestinal epithelium in response to radiation and protecting against radiation-induced GI syndrome.
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