Neidhart, M; Karouzakis, E; Schumann, G G; Gay, R E; Gay, S (2010). Trex-1 deficiency in rheumatoid arthritis synovial fibroblasts. Arthritis and Rheumatism, 62(9):2673-2679.
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Abstract
OBJECTIVE: To explore whether the increased expression of long interspersed nuclear element 1 (LINE-1; L1) messenger RNA (mRNA) and protein in rheumatoid arthritis synovial fibroblasts (RASFs) is associated with decreased expression of Trex-1, an exonuclease involved in the metabolization of L1 DNA:RNA hybrids. METHODS: Chromatin immunoprecipitation was used to detect L1-related p40 protein (L1-ORF1p) binding sequences in RASFs. Luciferase activity was measured in the synovial fibroblasts following cotransfection of the episomal plasmid with pJM105 expressing L1-ORF1p and pGL3-TS3 carrying the target sequence for L1-ORF1p. This luciferase reporter assay was used to compare the activity between RASFs and osteoarthritis synovial fibroblasts (OASFs) and to assess correlations of luciferase activity with the expression of Trex-1 measured by flow cytometry. The expression of Trex-1 mRNA and protein was also compared using real-time polymerase chain reaction, immunohistochemistry, and Western blot analyses. The role of Trex-1 in the L1-ORF1p-mediated luciferase activity assay was studied using interfering RNAs (iRNA) and a Trex-1 expression vector. RESULTS: Increased luciferase activity occurred after cotransfection of synovial fibroblasts with pJM105 and pGL3-TS3. L1-ORF1p activity was increased in RASFs as compared with OASFs, and this was correlated inversely with the expression of Trex-1. Levels of Trex-1 mRNA and protein were lower in RASFs than in OASFs. After transfection of the L1 expression plasmid, Trex-1 mRNA levels increased in OASFs, but not in RASFs. The addition of iRNA against Trex-1, however, resulted in an enhancement of L1-ORF1p activity in OASFs to the levels measured in RASFs. Overexpression of Trex-1 inhibited 5-azacytidine-induced expression of p38δ MAPK, a gene carrying the TS3 sequence. CONCLUSION: The deficiency of Trex-1 in RASFs allows a longer half-life of gene products encoded by active endogenous L1 retrotransposons. This pathway may play a role in diseases in which the cells exhibit a "spontaneous" aggressive behavior.
| Item Type: | Journal Article, refereed, original work |
|---|---|
| Communities & Collections: | 04 Faculty of Medicine > Center for Integrative Human Physiology 04 Faculty of Medicine > University Hospital Zurich > Rheumatology Clinic and Institute of Physical Medicine |
| DDC: | 570 Life sciences; biology 610 Medicine & health |
| Language: | English |
| Date: | September 2010 |
| Deposited On: | 24 Nov 2010 17:39 |
| Last Modified: | 23 Nov 2012 15:06 |
| Publisher: | Wiley-Blackwell |
| ISSN: | 0004-3591 |
| Free access at: | Publisher DOI. An embargo period may apply. |
| Publisher DOI: | 10.1002/art.27567 |
| PubMed ID: | 20496420 |
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