Immunohistochemical localisation of protein tyrosine kinase receptors Tie-1 and Tie-2 in synovial tissue of rheumatoid arthritis: correlation with angiogenesis and synovial proliferation
- Takeshi Uchidaa,
- Masahiro Nakashimab,
- Yashuhiro Hirotaa,
- Yoichi Miyazakia,
- Tomoo Tsukazakic,
- Hiroyuki Shindoa
- aDepartment of Orthopaedic Surgery, Nagasaki University School of Medicine, Nagasaki, Japan, bDepartment of Molecular Pathology, Atomic Bomb Disease Institute, Nagasaki University School of Medicine, Nagasaki, Japan, cFirst Department of Anatomy, Nagasaki University School of Medicine, Nagasaki, Japan
- Dr Tomoo Tsukazaki, First Department of Anatomy, Nagasaki University School of Medicine, 1–12–4 Sakamoto, Nagasaki 852–8523, Japan Email: ttsukanet{at}nagasaki-ac.jp
- Accepted 9 February 2000
Abstract
OBJECTIVE To investigate the involvement of Tie-1 and Tie-2, receptor tyrosine kinases required for angiogenesis, in synovial proliferation and angiogenesis of rheumatoid arthritis (RA).
METHODS Synovial tissues from 10 patients with RA and three control subjects were analysed by double immunohistochemistry and reverse transcriptase polymerase chain reaction (RT-PCR).
RESULTS Expression of Tie-1 and Tie-2 was seen in all synovia, but predominantly in papillary projected portions. In synovial lining cells, Tie-2 was expressed mainly in the basal layer and frequently colocalised with vimentin and proliferating cell nuclear antigen (PCNA), whereas Tie-1 was also expressed in the superficial layer. In stromal cells, Tie-2 immunoreactivity was restricted to vimentin positive fibroblast—but not macrophage derived cells, whereas Tie-1 expression was not dependent on the phenotype. Tie receptors were also highly expressed in the endothelium and surrounding pericytes of capillaries scattered over the papillary proliferated synovium without notable difference in the expression of the two receptors. Furthermore, Tie positive vessels often overexpressed PCNA. In normal synovia, expression of Tie receptors was restricted to the capillary endothelium. RT-PCR confirmed the expression of Tie-1 and Tie-2 in RA synovial tissues and also in the cultured synoviocytes.
CONCLUSION The results suggest the possible involvement of overexpressed Tie-1 and Tie-2 in synovial lining and stromal cells in the pathophysiology of RA synovitis, probably through distinct mechanisms. Furthermore, expression of Tie receptors in actively growing vasculature may reflect the direct involvement of these receptors in angiogenesis and subsequent vascularisation.
