GLIOSTATIN PLATELET-DERIVED ENDOTHELIAL-CELL GROWTH-FACTOR AS A CLINICAL MARKER OF RHEUMATOID-ARTHRITIS AND ITS REGULATION IN FIBROBLAST-LIKE SYNOVIOCYTES/
Y. Waguri et al., GLIOSTATIN PLATELET-DERIVED ENDOTHELIAL-CELL GROWTH-FACTOR AS A CLINICAL MARKER OF RHEUMATOID-ARTHRITIS AND ITS REGULATION IN FIBROBLAST-LIKE SYNOVIOCYTES/, British journal of rheumatology, 36(3), 1997, pp. 315-321
The objective was to assess the congruity of gliostatin/platelet-deriv
ed endothelial cell growth factor (GLS/PD-ECGF) with other clinical ma
rkers of rheumatoid arthritis (RA) and to define its molecular mechani
sm of action in the complicated cytokine network during RA pathogenesi
s. Immunoassay systems were used to quantify GLS or cytokine levels in
laboratory and clinical samples. Expression levels of GLS were determ
ined by reverse transcription-polymerase chain reaction methods. The G
LS levels in synovial fluid were correlated with interleukin-1 (IL-1)
and IL-8. The serial data of serum GLS levels reflected well changes i
n the disease activity during the clinical course of four representati
ve patients with RA, In cultured fibroblast-like synoviocytes, tumour
necrosis factor-alpha (TNF-alpha), IL-1, IL-6 and IL-8 induced GLS exp
ression. In conclusion, our results suggest that the serum GLS level,
mostly derived from cytokine-stimulated synoviocytes, was a useful cli
nical marker of RA.