TY - JOUR
T1 - The mRNA-binding protein IGF2BP1 maintains intestinal barrier function by up-regulating Occludin expression
AU - Singh, Vikash
AU - Gowda, Chethana P.
AU - Singh, Vishal
AU - Ganapathy, Ashwinkumar S.
AU - Karamchandani, Dipti M.
AU - Eshelman, Melanie A.
AU - Yochum, Gregory S.
AU - Nighot, Prashant
AU - Spiegelman, Vladimir S.
N1 - Publisher Copyright:
© 2020 American Society for Biochemistry and Molecular Biology Inc.. All rights reserved.
PY - 2020/6
Y1 - 2020/6
N2 - Insulin-like growth factor 2 mRNA-binding protein 1 (IGF2BP1) is an mRNA-binding protein that has an oncofetal pattern of expression. It is also expressed in intestinal tissue, suggesting that it has a possible role in intestinal homeostasis. To investigate this possibility, here we generated Villin CreERT2:Igf2bp1flox/flox mice, which enabled induction of an IGF2BP1 knockout specifically in intestinal epithelial cells (IECs) of adult mice. Using gut barrier and epithelial permeability assays and several biochemical approaches, we found that IGF2BP1 ablation in the adult intestinal epithelium causes mild active colitis and mild-to-moderate active enteritis. Moreover, the IGF2BP1 deletion aggravated dextran sodium sulfate (DSS)-induced colitis. We also found that IGF2BP1 removal compromises barrier function of the intestinal epithelium, resulting from altered protein expression at tight junctions. Mechanistically, IGF2BP1 interacted with the mRNA of the tight-junction protein Occludin (Ocln), stabilizing Ocln mRNA and inducing expression of Occludin in IECs. Furthermore, ectopic Occludin expression in IGF2BP1-knockdown cells restored barrier function. We conclude that IGF2BP1-dependent regulation of Occludin expression is an important mechanism in intestinal barrier function maintenance and in the prevention of colitis.
AB - Insulin-like growth factor 2 mRNA-binding protein 1 (IGF2BP1) is an mRNA-binding protein that has an oncofetal pattern of expression. It is also expressed in intestinal tissue, suggesting that it has a possible role in intestinal homeostasis. To investigate this possibility, here we generated Villin CreERT2:Igf2bp1flox/flox mice, which enabled induction of an IGF2BP1 knockout specifically in intestinal epithelial cells (IECs) of adult mice. Using gut barrier and epithelial permeability assays and several biochemical approaches, we found that IGF2BP1 ablation in the adult intestinal epithelium causes mild active colitis and mild-to-moderate active enteritis. Moreover, the IGF2BP1 deletion aggravated dextran sodium sulfate (DSS)-induced colitis. We also found that IGF2BP1 removal compromises barrier function of the intestinal epithelium, resulting from altered protein expression at tight junctions. Mechanistically, IGF2BP1 interacted with the mRNA of the tight-junction protein Occludin (Ocln), stabilizing Ocln mRNA and inducing expression of Occludin in IECs. Furthermore, ectopic Occludin expression in IGF2BP1-knockdown cells restored barrier function. We conclude that IGF2BP1-dependent regulation of Occludin expression is an important mechanism in intestinal barrier function maintenance and in the prevention of colitis.
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U2 - 10.1074/jbc.ac120.013646
DO - 10.1074/jbc.ac120.013646
M3 - Article
C2 - 32385106
AN - SCOPUS:85086793100
SN - 0021-9258
VL - 295
SP - 8602
EP - 8612
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 25
ER -