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- Title
Hemin and a metabolic derivative coprohemin modulate the TLR4 pathway differently through different molecular targets.
- Authors
Piazza, Matteo; Damore, Gaetana; Costa, Barbara; Gioannini, Theresa L.; Weiss, Jerrold P.; Peri, Francesco
- Abstract
Heme is a prosthetic group in a large number of essential proteins that have a pivotal role in oxygen transport, storage and electron shuttling. High amounts of free heme are associated with pathological states. Recently, it has been suggested that activation of Toll-like receptor 4 (TLR4) is one of the ways in which the ‘danger signal’ of free heme is detected. Here, we examine the biochemical basis of the modulation of the TLR4 pathway by hemin (iron(III)-protoporphyrin IX) and its metabolic, oxidated derivative coprohemin (iron(III)-coproporphyrin I). High concentrations of hemin (50 μM) triggered TLR4-mediated IL-8 production in the human HEK293/TLR4 cell line in the absence of the co-receptors CD14 and MD-2; the latter an essential co-receptor for TLR4 activation by endotoxin. Hemin and endotoxin have additive effects when co-administrated to HEK/TLR4 cells, suggesting that hemin and endotoxin activate TLR4 by different mechanisms. Coprohemin, in contrast to hemin, is unable to trigger TLR4-dependent activation of HEK/TLR4 cells, but instead causes dose-dependent inhibition of endotoxin-stimulated IL-8 production. The inhibitory effect of coprohemin is paralleled by reduced delivery of endotoxin to MD-2 (-TLR4) that is necessary for activation of TLR4 by endotoxin. Thus, despite their similar chemical structure, hemin and coprohemin have very different effects on the TLR4 pathway, the former acting as a mild agonist of TLR4, the latter as an antagonist selectively targeting the endotoxin—MD-2 interaction.
- Subjects
CELL receptors; HEME; ENDOTOXINS; PHYSIOLOGICAL transport of oxygen; BIOCHEMISTRY; INTERLEUKIN-8; CELL lines
- Publication
Innate Immunity, 2011, Vol 17, Issue 3, p293
- ISSN
1753-4259
- Publication type
Article
- DOI
10.1177/1753425910369020