d-Glycero-β-d-Manno-Heptose 1-Phosphate and d-Glycero-β-d-Manno-Heptose 1,7-Biphosphate Are Both Innate Immune Agonists.
Itunuoluwa A AdekoyaCynthia Xinyi GuoScott D Gray-OwenAndrew D CoxJanelle SauvageauPublished in: Journal of immunology (Baltimore, Md. : 1950) (2018)
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.
Keyphrases
- innate immune
- oxidative stress
- gram negative
- multidrug resistant
- induced apoptosis
- cell cycle arrest
- structure activity relationship
- diabetic rats
- endothelial cells
- signaling pathway
- molecular docking
- microbial community
- high glucose
- ms ms
- cell death
- lps induced
- immune response
- pi k akt
- endoplasmic reticulum stress
- toll like receptor
- inflammatory response
- single molecule
- induced pluripotent stem cells