Toll-like receptors mediate induction of hepcidin in mice infected with Borrelia burgdorferi.

Abstract

Hepcidin is the major regulator of systemic iron homeostasis in mammals. Hepcidin is produced mainly by the liver and is increased by inflammation, leading to hypoferremia. We measured serum levels of bioactive hepcidin and its effects on serum iron levels in mice infected with Borrelia burgdorferi. Bioactive hepcidin was elevated in the serum of mice resulting in hypoferremia. Infected mice produced hepcidin in both liver and spleen. Both intact and sonicated B burgdorferi induced hepcidin expression in cultured mouse bone marrrow macrophages. Hepcidin production by cultured macrophages represents a primary transcriptional response stimulated by B burgdorferi and not a secondary consequence of cytokine elaboration. Hepcidin expression induced by B burgdorferi was mediated primarily by activation of Toll-like receptor 2.

• Authors: Curry L Koening, Jennifer C Miller, Jenifer M Nelson, Diane M Ward, James P Kushner, Linda K Bockenstedt, Janis J Weis, Jerry Kaplan, Ivana De Domenico
• Journal: Blood (Blood) Vol. 114 Issue 9 Pg. 1913-8 (Aug 27 2009) ISSN: 1528-0020 [Electronic] United States
• PMID: 19587376 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Antimicrobial Cationic Peptides
• Cytokines
• HAMP protein, human
• Hamp protein, mouse
• Hepcidins
• Toll-Like Receptor 2
• Toll-Like Receptors
• Green Fluorescent Proteins

Topics

• Animals
• Antimicrobial Cationic Peptides (metabolism)
• Bone Marrow Cells (cytology)
• Borrelia burgdorferi (metabolism)
• Cytokines (metabolism)
• Green Fluorescent Proteins (metabolism)
• Hepcidins
• Humans
• Inflammation
• Macrophages (metabolism)
• Mice
• Mice, Inbred C57BL
• Mice, Transgenic
• Models, Biological
• Toll-Like Receptor 2 (metabolism)
• Toll-Like Receptors (metabolism)