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Sung-Hoon Ahn, Yatrik M. Shah, Junko Inoue, Keiichirou Morimura, Insook Kim, SunHee Yim, Gilles Lambert, Reiko Kurotani, Kunio Nagashima, Frank J. Gonzalez, Yusuke Inoue, Hepatocyte nuclear factor 4α in the intestinal epithelial cells protects against inflammatory bowel disease, Inflammatory Bowel Diseases, Volume 14, Issue 7, 1 July 2008, Pages 908–920, https://doi.org/10.1002/ibd.20413
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Hepatocyte nuclear factor 4α (HNF4α; NR2A1) is an orphan member of the nuclear receptor superfamily expressed in liver and intestine. While HNF4α expression is critical for liver function, its role in the gut and in the pathogenesis of inflammatory bowel disease (IBD) is unknown.
Human intestinal biopsies from control and IBD patients were examined for expression of mRNAs encoding HNF4α and other nuclear receptors. An intestine-specific HNF4α null mouse line (Hnf4αΔIEpC) was generated using an Hnf4α-floxed allele and villin-Cre transgene. These mice and their control floxed counterparts (Hnf4αF/F), were subjected to a dextran sulfate sodium (DSS)-induced IBD colitis protocol and their clinical symptoms and gene expression patterns determined.
In human intestinal biopsies, HNF4α was significantly decreased in intestinal tissues from Crohn's disease and ulcerative colitis patients. HNF4α expression was also suppressed in the intestine of DSS-treated mice. In Hnf4αΔIEpC mice, disruption of HNF4α expression was observed in the epithelial cells throughout the intestine. In the DSS-induced colitis model Hnf4αΔIEpC mice showed markedly more severe changes in clinical symptoms and pathologies associated with IBD including loss of body weight, colon length, and histological morphology as compared with Hnf4αF/F mice. Furthermore, the Hnf4αΔIEpC mice demonstrate a significant alteration of mucin-associated genes and increased intestinal permeability, which may play an important role in the increased susceptibility to acute colitis following an inflammatory insult.
While HNF4α does not have a major role in normal function of the intestine, it protects the gut against DSS-induced colitis.
