期刊
ELIFE
卷 4, 期 -, 页码 -出版社
ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.05648
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资金
- Wellcome Trust DBT India Alliance, intermediate fellowship
- National Institute of Immunology
- Council of Scientific and Industrial Research (CSIR)
Tissue microenvironment functions as an important determinant of the inflammatory response elicited by the resident cells. Yet, the underlying molecular mechanisms remain obscure. Our systems-level analyses identified a duration code that instructs stimulus specific crosstalk between TLR4-activated canonical NF-kappa B pathway and lymphotoxin-beta receptor (LT beta R) induced non-canonical NF-kappa B signaling. Indeed, LT beta R costimulation synergistically enhanced the late RelA/NF-kappa B response to TLR4 prolonging NF-kappa B target gene-expressions. Concomitant LT beta R signal targeted TLR4-induced newly synthesized p100, encoded by Nfkb2, for processing into p52 that not only neutralized p100 mediated inhibitions, but potently generated RelA: p52/NF-kappa B activity in a positive feedback loop. Finally, Nfkb2 connected lymphotoxin signal within the intestinal niche in reinforcing epithelial innate inflammatory RelA/NF-kappa B response to Citrobacter rodentium infection, while Nfkb2(-/-) mice succumbed to gut infections owing to stromal defects. In sum, our results suggest that signal integration via the pleiotropic NF-kappa B system enables tissue microenvironment derived cues in calibrating physiological responses. DOI: 10.7554/eLife.05648.001
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