期刊
STEM CELL REPORTS
卷 15, 期 2, 页码 389-407出版社
CELL PRESS
DOI: 10.1016/j.stemcr.2020.06.017
关键词
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资金
- Crohn's and Colitis Foundation Career Development Award [370615]
- NIH [K08DK110421, P30DK097948, DK042191, DK091222, DK07948, R01AI145289-01A1]
Intestinal epithelial barrier dysfunction is a risk factor in the pathogenesis of Crohn's disease (CD); however, no corrective FDA-approved therapies exist. We used an enteroid (EnO)-based system in two murine models of experimental CD, SAMP1/YitFc (SAMP) and TNFDARE/(+) (TNF). While severely inflamed SAMP mice do not generate EnOs, inflammation-freeSAMP mice form EnO structures with impaired morphology and reduced intestinal stem cell (ISC) and Paneth cell viability. We validated these findings in TNF mice concluding that inflammation in intestinal tissues impedes EnO generation and suppressing inflammation by steroid administration partially rescues impaired formation in SAMP mice. We generated the first high-resolution transcriptional profile of the SAMP ISC niche demonstrating that alterations in multiple key pathways contribute to niche defect and targeting them may partially rescue the phenotype. Furthermore, we correlated the defects in formation and the rescue of EnO formation to reduced viability of ISCs and Paneth cells.
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