miR-146a mediates protective innate immune tolerance in the neonate intestine - PubMed (original) (raw)
. 2010 Oct 21;8(4):358-68.
doi: 10.1016/j.chom.2010.09.005.
Affiliations
- PMID: 20951969
- DOI: 10.1016/j.chom.2010.09.005
Free article
miR-146a mediates protective innate immune tolerance in the neonate intestine
Cécilia Chassin et al. Cell Host Microbe. 2010.
Free article
Abstract
After birth, the intestinal mucosa undergoes a dramatic transition from a sterile protected site to an environmentally exposed and permanently colonized surface. The mechanisms that facilitate this transition are ill defined. Here, we demonstrate that microRNA-146a-mediated translational repression and proteolytic degradation of the essential Toll-like receptor (TLR) signaling molecule interleukin 1 receptor associated kinase 1 (IRAK1) is sufficient to induce intestinal epithelial innate immune tolerance and provide protection from bacteria-induced epithelial damage in neonates. Despite low IRAK1 protein levels, continuous TLR4- and IRAK1-dependent signal transduction induced by intraepithelial endotoxin persistence during the neonatal period maintains tolerance through sustained miR-146a expression. Strikingly, it additionally facilitates transcription of a distinct set of genes involved in cell survival, differentiation, and homeostasis. Thus, our results identify the underlying molecular mechanisms of intestinal epithelial innate immune tolerance during the neonatal period and characterize tolerance as an active condition involved in the establishment of intestinal mucosal homeostasis.
Copyright © 2010 Elsevier Inc. All rights reserved.
Comment in
- MicroRNAs and LPS: developing a relationship in the neonatal gut.
Barbalat R, Barton GM. Barbalat R, et al. Cell Host Microbe. 2010 Oct 21;8(4):303-4. doi: 10.1016/j.chom.2010.10.001. Cell Host Microbe. 2010. PMID: 20951963 - (micro)Tolerance in the gut.
Leavy O. Leavy O. Nat Rev Immunol. 2010 Dec;10(12):810. doi: 10.1038/nri2894. Nat Rev Immunol. 2010. PMID: 21155195 No abstract available.
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