| Literature DB >> 30224513 |
Itunuoluwa A Adekoya1, Cynthia X Guo1, Scott D Gray-Owen1, Andrew D Cox2, Janelle Sauvageau3.
Abstract
d-Glycero-β-d-manno-heptose 1,7-biphosphate (β-HBP) is a novel microbial-associated molecular pattern that triggers inflammation and thus has the potential to act as an immune modulator in many therapeutic contexts. To better understand the structure-activity relationship of this molecule, we chemically synthesized analogs of β-HBP and tested their ability to induce canonical TIFA-dependent inflammation in human embryonic kidney cells (HEK 293T) and colonic epithelial cells (HCT 116). Of the analogs tested, only d-glycero-β-d-manno-heptose 1-phosphate (β-HMP) induced TIFA-dependent NF-κB activation and cytokine production in a manner similar to β-HBP. This finding expands the spectrum of metabolites from the Gram-negative ADP-heptose biosynthesis pathway that can function as innate immune agonists and provides a more readily available agonist of the TIFA-dependent inflammatory pathway that can be easily produced by synthetic methods.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30224513 DOI: 10.4049/jimmunol.1801012
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422