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Recognition of Hyaluronan Released in Sterile Injury Involves a Unique Receptor Complex Dependent on Toll-like Receptor 4, CD44, and MD-2*
Kristen R. Taylor,
Kenshi Yamasaki,
Katherine A. Radek,
Anna Di Nardo,
Heidi Goodarzi,
Douglas Golenbock,
Bruce Beutler¶, , and
Richard L. Gallo1
Division of Dermatology, University of California, San Diego and Veterans Affairs Medical Center, San Diego, California 92161, the Division of Infectious Disease and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, Massachusetts 01605, and the ¶Department of Immunology, The Scripps Research Institute, La Jolla, California 92037
Abstract:
Inflammation under sterile conditions is not well understooddespite its importance in trauma and autoimmune disease. Toinvestigate this process we established mouse models of sterileinjury and explored the role of hyaluronan in mediating inflammationfollowing injury. The response of cultured monocytes to hyaluronanwas different than the response to lipopolysaccharide (LPS)despite both being dependent on Toll-like receptor 4 (TLR4).Cultured cells exposed to hyaluronan showed a pattern of geneinduction that mimics the response seen in mouse skin aftersterile injury with an increase in molecules such as transforminggrowth factor-2 and matrix metalloproteinase-13. These factorswere not induced by LPS despite the mutual dependence of bothhyaluronan and LPS on TLR4. Explanation for the unique responseto hyaluronan was provided by observations that a lack of TLR4or CD44 in mice diminished the response to sterile injury, andtogether with MD-2, was required for responsiveness to hyaluronanin vitro. Thus, a unique complex of TLR4, MD-2, and CD44 recognizeshyaluronan. Immunoprecipitation experiments confirmed the physicalassociation of TLR4 and CD44. Taken together, our results definea previously unknown mechanism for initiation of sterile inflammationthat involves recognition of released hyaluronan fragments asan endogenous signal of tissue injury.
Received for publication July 3, 2006.
Revision received March 28, 2007.
* The costs of publication of this article were defrayed in partby the payment of page charges. This article must thereforebe hereby marked "advertisement" in accordance with 18 U.S.C.Section 1734 solely to indicate this fact.
The on-line version of this article (available at http://www.jbc.org)contains supplemental Table S1 and Fig. S1.
1 To whom correspondence should be addressed: Division of Dermatology, University of California, MC 9111B, 3350 La Jolla Village Dr., San Diego, CA 92161. Tel.: 858-642-3504; Fax: 858-642-1435; E-mail: rgallo{at}vapop.ucsd.edu.
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