Abstract
Abstract The agent of Lyme disease, Borrelia burgdorferi, produces membrane lipoproteins possessing potent inflammatory properties linked to disease pathology. The recent association of toll-like receptors (TLR) 2 and 4 with LPS responses prompted the examination of TLR involvement in lipoprotein signaling. The ability of human cell lines to respond to lipoproteins was correlated with the expression of TLR2. Transfection of TLR2 into cell lines conferred responsiveness to lipoproteins, lipopeptides, and sonicated B. burgdorferi, as measured by nuclear translocation of NF-κB and cytokine production. The physiological importance of this interaction was demonstrated by the 10-fold greater sensitivity of TLR2-transfected cells to lipoproteins than LPS. Futhermore, TLR2-dependant signaling by lipoproteins was facilitated by CD14. These data indicate that TLR2 facilitates the inflammatory events associated with Lyme arthritis. In addition, the widespread expression of lipoproteins by other bacterial species suggests that this interaction may have broad implications in microbial inflammation and pathogenesis.
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Dates
Type | When |
---|---|
Created | 2 years, 8 months ago (Dec. 31, 2022, 11:06 a.m.) |
Deposited | 5 months ago (March 31, 2025, 8:43 a.m.) |
Indexed | 4 hours, 31 minutes ago (Sept. 3, 2025, 7:16 a.m.) |
Issued | 26 years ago (Sept. 1, 1999) |
Published | 26 years ago (Sept. 1, 1999) |
Published Online | 26 years ago (Sept. 1, 1999) |
Published Print | 26 years ago (Sept. 1, 1999) |
@article{Hirschfeld_1999, title={Cutting Edge: Inflammatory Signaling by Borrelia burgdorferi Lipoproteins Is Mediated by Toll-Like Receptor 2}, volume={163}, ISSN={1550-6606}, url={http://dx.doi.org/10.4049/jimmunol.163.5.2382}, DOI={10.4049/jimmunol.163.5.2382}, number={5}, journal={The Journal of Immunology}, publisher={Oxford University Press (OUP)}, author={Hirschfeld, Matthew and Kirschning, Carsten J and Schwandner, Ralf and Wesche, Holger and Weis, John H and Wooten, R Mark and Weis, Janis J}, year={1999}, month=sep, pages={2382–2386} }