Expression of transient receptor potential vanilloid 1 (TRPV1) in synovial fibroblasts from patients with osteoarthritis and rheumatoid arthritis

被引:113
作者
Engler, Andrea
Aeschlimann, Andre
Simmen, Beat R.
Michel, Beat A.
Gay, Renate E.
Gay, Steffen
Sprott, Haiko
机构
[1] ETH, CH-8092 Zurich, Switzerland
[2] Univ Hosp, Ctr Expt Rheumatol, Inst Med Phys, Dept Rheumatol, Zurich, Switzerland
[3] Univ Zurich, Ctr Integrat Human Physiol, Zurich, Switzerland
[4] RehaClin Zurzach, CH-5330 Zurzach, Switzerland
[5] Shulthess Clin, CH-8008 Zurich, Switzerland
关键词
transient receptor potential vanilloid 1; vanilloid receptor; TRPV1; capsaicin; capsazepine; synovial fibroblast; osteoarthritis; rheumatoid arthritis; gene expression; real-time PCR;
D O I
10.1016/j.bbrc.2007.05.178
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The transient receptor potential vanilloid 1 (TRPV1) is a nonselective cation channel, which is mainly expressed by nociceptive neurons in dorsal root and trigeminal ganglia. However, there is increasing evidence that TRPV1 expression is not limited to primary afferent neurons but that the receptor is expressed in various cell types throughout the body. Here, we demonstrate the expression of TRPV1 in synovial fibroblasts (SF) from patients with symptomatic osteoarthritis (OA) and rheumatoid arthritis (RA). In addition, the mRNA expression of TRPV1 was shown in PBMCs from healthy controls and from OA patients. The presence of TRPV1 was confirmed at the protein level. Stimulation of cultured OA- and RA-SF with the TRPV1 agonist capsaicin led to increased expression of IL-6 mRNA as well as of IL-6 protein in the cell culture supernatants. IL-6 protein expression could be antagonized with capsazepine. Thus, we hypothesize that TRPV1 may play a role in non-neuronal mechanisms that might modulate nociception in symptomatic OA and RA patients. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:884 / 888
页数:5
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