COCULTURE OF SYNOVIAL FIBROBLASTS AND DIFFERENTIATED U937 CELLS IS SUFFICIENT FOR HIGH INTERLEUKIN-6 BUT NOT INTERLEUKIN-1-BETA OR TUMOR-NECROSIS-FACTOR-ALPHA RELEASE
V. Chen et al., COCULTURE OF SYNOVIAL FIBROBLASTS AND DIFFERENTIATED U937 CELLS IS SUFFICIENT FOR HIGH INTERLEUKIN-6 BUT NOT INTERLEUKIN-1-BETA OR TUMOR-NECROSIS-FACTOR-ALPHA RELEASE, British journal of rheumatology, 37(2), 1998, pp. 148-156
Inflamed synovium is characterized by high concentrations of cytokines
[interleukin (IL)-6, IL-1 beta and tumour necrosis factor (TNF)-alpha
] and the abundant presence of infiltrated monocytes, many of which ar
e found adjacent to the resident fibroblast-like synoviocytes. We have
used a co-culture of fibroblast-like synoviocytes and differentiated
U937 cells to study IL-6, IL-1 beta and TNF-alpha release. After a 3 d
ay co-culture, 35% of the U937 cells had adhered and were fully differ
entiated towards monocytes, as determined by expression of p47(phox),
CD14, MSE-1, Mac-1, collagenase and NADPH oxidase activity. IL-6 relea
se from fibroblast-like synoviocytes was induced 4-fold by co-culture
with differentiated U937 cells. However, co-culture of differentiated
U937 cells with fibroblast-like synoviocytes failed to release detecta
ble levels of IL-1 beta and TNF-alpha from the U937 cells. Addition of
synovial fluid further increased IL-6 release, bur again had no effec
t on IL-1 beta or TNF-alpha, although U937 cells differentiated by pho
rbol ester were able to release these two cytokines and, in the case o
f the co-culture, mRNAs for both cytokines were highly expressed in th
e U937 cells. We postulate that the influx of monocytes into the synov
ium is instrumental in the elevation of IL-6 levels, but this is not s
ufficient to explain high levels of IL-1 beta or TNF-alpha.