| Literature DB >> 11213361 |
Y Hirai1, K Migita, S Honda, Y Ueki, S Yamasaki, S Urayama, M Kamachi, A Kawakami, H Ida, M Kita, T Fukuda, K Shibatomi, Y Kawabe, T Aoyagi, K Eguchi.
Abstract
Nitric oxide (NO) is a multifunctional messenger molecule generated from L-arginine by a family of enzymes, including nitric oxide synthase (NOS). This study was performed to examine whether NO modulates the production of matrix metalloproteinases (MMPs), which degrade all components of extracellular matrix (ECM), in rheumatoid synovial cells. We investigated the effects of exogenously generated NO by a NO donor, S-nitroso-N-acetyl-DL-penicillamine (SNAP), on the MMPs production by rheumatoid synovial cells. Culture media conditioned by SNAP-treated synovial cells were examined by gelatin zymography and immunoblot analysis. Incubation of synovial cells with SNAP resulted in gelatinase A production in a dose-dependent fashion. Furthermore, RT-PCR analysis demonstrated that MMP-2 mRNA expression was induced in SNAP-treated synovial cells. In contrast, SNAP did not influence the production of TIMP-1 and TIMP-2, which preferentially inhibit MMP-2, by rheumatoid synovial cells. Our data indicate that NO could modulate MMP production by rheumatoid synovial cells and therefore contribute to ECM degradation of articular components in RA.Entities:
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Year: 2001 PMID： 11213361 DOI： 10.1016/s0024-3205(00)00998-x
Source DB: PubMed Journal: Life Sci ISSN： 0024-3205 Impact factor: 5.037