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PMID: 16142712 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Innate immunity conferred by Toll-like receptors 2 and 4 and myeloid differentiation factor 88 expression is pivotal to monosodium urate monohydrate crystal-induced inflammation.

Arthritis and rheumatism ·Vol. 52 ·No. 9 ·2005-09-00 ·Pages 2936-46

Liu-Bryan R, Scott P, Sydlaske A, Rose DM, Terkeltaub R

Abstract

In gout, incompletely defined molecular factors alter recognition of dormant articular and bursal monosodium urate monohydrate (MSU) crystal deposits, thereby inducing self-limiting bouts of characteristically severe neutrophilic inflammation. To define primary determinants of cellular recognition, uptake, and inflammatory responses to MSU crystals, we conducted a study to test the role of Toll-like receptor 2 (TLR-2), TLR-4, and the cytosolic TLR adapter protein myeloid differentiation factor 88 (MyD88), which are centrally involved in innate immune recognition of microbial pathogens. We isolated bone marrow-derived macrophages (BMDMs) in TLR-2-/-, TLR-4-/-, MyD88-/-, and congenic wild-type mice, and assessed phagocytosis and cytokine expression in response to endotoxin-free MSU crystals under serum-free conditions. MSU crystals also were injected into mouse synovium-like subcutaneous air pouches. TLR-2-/-, TLR-4-/-, and MyD88-/- BMDMs demonstrated impaired uptake of MSU crystals in vitro. MSU crystal-induced production of interleukin-1beta (IL-1beta), tumor necrosis factor alpha, keratinocyte-derived cytokine/growth-related oncogene alpha, and transforming growth factor beta1 also were significantly suppressed in TLR-2-/- and TLR-4-/- BMDMs and were blunted in MyD88-/- BMDMs in vitro. Neutrophil influx and local induction of IL-1beta in subcutaneous air pouches were suppressed 6 hours after injection of MSU crystals in TLR-2-/- and TLR-4-/- mice and were attenuated in MyD88-/- mice. The murine host requires TLR-2, TLR-4, and MyD88 for macrophage activation and development of full-blown neutrophilic, air pouch inflammation in response to MSU crystals. Our findings implicate innate immune cellular recognition of naked MSU crystals by specific TLRs as a major factor in determining the inflammatory potential of MSU crystal deposits and the course of gouty arthritis.

MeSH Terms
Adaptor Proteins, Signal Transducing Animals Antigens, Differentiation/genetics,metabolism Arthritis, Gouty/genetics,immunology,metabolism Bone Marrow Cells/drug effects,metabolism Cytokines/metabolism Disease Models, Animal Immunity, Innate/immunology Macrophages/drug effects,metabolism Mice Mice, Inbred C57BL Mice, Knockout Myeloid Differentiation Factor 88 Phagocytosis/drug effects Receptors, Immunologic/genetics,metabolism Specific Pathogen-Free Organisms Toll-Like Receptor 2 Toll-Like Receptor 4 Uric Acid/immunology,toxicity
Chemicals
Adaptor Proteins, Signal Transducing Antigens, Differentiation Cytokines Myd88 protein, mouse Myeloid Differentiation Factor 88 Receptors, Immunologic Tlr2 protein, mouse Tlr4 protein, mouse Toll-Like Receptor 2 Toll-Like Receptor 4 Uric Acid
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Liu-Bryan Ru
VA Medical Center, University of California, San Diego 92161, USA. [email protected]
Scott Peter
Sydlaske Anya
Rose David M
Terkeltaub Robert
Article Info
Journal
Arthritis and rheumatism
Abbr.
Arthritis Rheum
ISSN
0004-3591
Published
2005-09-00
Pages
2936-46
Language
English
Region
United States
NLM ID
0370605
Subset
IM
Grants
NIAMS NIH HHS · AR-049416 · United States
NHLBI NIH HHS · HL-077360 · United States
NIAMS NIH HHS · P30-AR-43360 · United States
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