Detection of oncofetal h19 RNA in rheumatoid arthritis synovial tissue.

Abstract

The expression of oncofetal H19 RNA and its localization/cellular source was analyzed in synovial tissue (ST) and isolated synovial macrophages (Mphi) or synovial fibroblasts (SFBs) by reverse transcriptase-polymerase chain reaction (RT-PCR), in situ hybridization, and immunohistochemistry. RT-PCR showed significantly higher H19 expression in ST from patients with rheumatoid arthritis (RA) (P = 0.000) and osteoarthritis (OA) (P = 0.009) than in normal/joint trauma controls (N/JT), but comparable levels in reactive arthritis. In situ hybridization demonstrated strong signals in all RA-ST samples (n = 8), with > or =85% positive cells in the lining layer, diffuse infiltrates, and stroma regions. In lymphoid aggregates and endothelial cells only 20% were positive. RA-ST contained a significantly higher percentage of strongly positive lining cells than OA-ST and N/JT-ST. H19 RNA was expressed in both Mphi and SFBs, as confirmed by RT-PCR in isolated RA Mphi and SFBs (n = 3). In RA-SFBs, low constitutive H19 RNA expression in culture (10% fetal calf serum) was strongly increased on starvation (3.5-fold, 1% fetal calf serum), with or without the addition of interleukin-1beta (10 to 100 U/ml), tumor necrosis factor-alpha (1 to 25 ng/ml), or platelet-derived growth factor-BB (2.5 to 10 U/ml). In OA-SFBs, this starvation-induced increase was lower (twofold), reaching significant differences compared with RA-SFBs after stimulation with interleukin-1beta and platelet-derived growth factor-BB. In both RA- and OA-SFBs, the MAP-kinase ERK-1/2 pathway and the phosphatidylinositol-3 kinase pathway influenced H19 RNA expression, as shown by inhibitor studies. Significant overexpression of H19 RNA and its increased sensitivity to starvation/cytokine regulation in RA suggests a pathogenetic role of this oncofetal gene, possibly reflecting embryonal dedifferentiation of the adult ST and/or ongoing inflammatory/oxidative stress.

• Authors: Bruno Stuhlmüller, Elke Kunisch, Juliane Franz, Lorena Martinez-Gamboa, Maria M Hernandez, Axel Pruss, Norbert Ulbrich, Volker A Erdmann, Gerd R Burmester, Raimund W Kinne
• Journal: The American journal of pathology (Am J Pathol) Vol. 163 Issue 3 Pg. 901-11 (Sep 2003) ISSN: 0002-9440 [Print] United States
• PMID: 12937131 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antigens, Neoplasm
• Culture Media
• H19 long non-coding RNA
• Interleukin-1
• Platelet-Derived Growth Factor
• Proto-Oncogene Proteins c-sis
• RNA, Long Noncoding
• RNA, Untranslated
• Tumor Necrosis Factor-alpha
• oncofetal antigens
• Becaplermin

Topics

• Adult
• Aged
• Antigens, Neoplasm (metabolism)
• Arthritis, Reactive (metabolism)
• Arthritis, Rheumatoid (metabolism)
• Becaplermin
• Case-Control Studies
• Cells, Cultured
• Culture Media (chemistry, pharmacology)
• Female
• Fibroblasts (drug effects, metabolism)
• Humans
• In Situ Hybridization (methods)
• Interleukin-1 (pharmacology)
• Joints (injuries)
• Macrophages (metabolism)
• Male
• Middle Aged
• Osteoarthritis (metabolism)
• Platelet-Derived Growth Factor (pharmacology)
• Proto-Oncogene Proteins c-sis
• RNA, Long Noncoding
• RNA, Untranslated (metabolism)
• Reverse Transcriptase Polymerase Chain Reaction
• Synovial Membrane (metabolism, pathology)
• Tumor Necrosis Factor-alpha (pharmacology)
• Wounds and Injuries (metabolism)