NOD-Like Receptors in Intestinal Homeostasis and Epithelial Tissue Repair

被引:72
作者
Parlato, Marianna [1 ]
Yeretssian, Garabet [1 ,2 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Med, Inst Immunol, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
关键词
nucleotide-binding and oligomerization domain-like receptors (NLRs); intestinal epithelial cells (IECs); wound healing; colitis; inflammatory bowel diseases (IBD); inflammasome; growth factors; innate immunity; toll-like receptors (TLRs); INFLAMMATORY-BOWEL-DISEASE; NF-KAPPA-B; EPIDERMAL-GROWTH-FACTOR; TOLL-LIKE RECEPTOR-4; GENOME-WIDE ASSOCIATION; COMPLEX INSERTION/DELETION POLYMORPHISM; SODIUM-SULFATE COLITIS; NECROSIS-FACTOR-ALPHA; CROHNS-DISEASE; IN-VITRO;
D O I
10.3390/ijms15069594
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The intestinal epithelium constitutes a dynamic physical barrier segregating the luminal content from the underlying mucosal tissue. Following injury, the epithelial integrity is restored by rapid migration of intestinal epithelial cells (IECs) across the denuded area in a process known as wound healing. Hence, through a sequence of events involving restitution, proliferation and differentiation of IECs the gap is resealed and homeostasis reestablished. Relapsing damage followed by healing of the inflamed mucosa is a hallmark of several intestinal disorders including inflammatory bowel diseases (IBD). While several regulatory peptides, growth factors and cytokines stimulate restitution of the epithelial layer after injury, recent evidence in the field underscores the contribution of innate immunity in controlling this process. In particular, nucleotide-binding and oligomerization domain-like receptors (NLRs) play critical roles in sensing the commensal microbiota, maintaining homeostasis, and regulating intestinal inflammation. Here, we review the process of intestinal epithelial tissue repair and we specifically focus on the impact of NLR-mediated signaling mechanisms involved in governing epithelial wound healing during disease.
引用
收藏
页码:9594 / 9627
页数:34
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