TY - JOUR
T1 - Human fibroblasts release reactive oxygen species in response to treatment with synovial fluids from patients suffering from arthritis
AU - Meier, Beate
AU - Radeke, Heinfried H.
AU - Selle, Susanne
AU - Raspe, H. H.
AU - Sies, Helmut
AU - Resch, Klaus
AU - Habermehl, Gerhard G.
N1 - Funding Information:
Supported by Deutsche Forschungsgemeinschaft: SFB 244/BI I. We appreciate the possibility to perform our cell cultures at the laboratories of Profs. E. Lamprecht (Hannover), W. Leibold (Hannover) and D. Beyersmann (Bremen) and we are grateful to the University of Bremen for providing the ESR spectrometer. Moreover, we wish to thank Dr. C. Baumstark-Khan (Bonn) for providing us with primary cultures of fibroblasts and Mrs. C. Bovenkerk and Mrs. E. Wobbecke for technical assistance. We are grateful to Dr. M. Murphy for help in the chemiluminescence assays.
PY - 1990
Y1 - 1990
N2 - Human fibroblasts in primary culture released reactive oxygen species upon exposure to synovial fluid obtained by joint aspiration from twelve patients suffering from rheumatoid arthritis. The primary radical produced was O-2 as determined by ESR spin trapping and cytochrome c reduction. In contrast to the oxidative burst in granulocytes and monocytes. radical formation proceeded continuously for at least four hours. Low-level chemiluminescence was increased upon exposure to inflammatory human synovial fluids. Spectral characteristics and effects of azide and 1,4-diazabicyclo-(2,2,2)-octane led to the conclusion that the photoemissive species were excited carbonyls. Radical production and light emission were not altered either by xanthine or allopurinol. nor by azide. cyanide or rotenone. The O-2; production increased in the presence of NADH or NADPH. making an NAD(P)H oxidase a likely source. The liberation of reactive oxygen species correlated with the number of leukocytes present in the inflammatory joint fluids. but not with the concentrations of immunoglobulins and complement factor C3.
AB - Human fibroblasts in primary culture released reactive oxygen species upon exposure to synovial fluid obtained by joint aspiration from twelve patients suffering from rheumatoid arthritis. The primary radical produced was O-2 as determined by ESR spin trapping and cytochrome c reduction. In contrast to the oxidative burst in granulocytes and monocytes. radical formation proceeded continuously for at least four hours. Low-level chemiluminescence was increased upon exposure to inflammatory human synovial fluids. Spectral characteristics and effects of azide and 1,4-diazabicyclo-(2,2,2)-octane led to the conclusion that the photoemissive species were excited carbonyls. Radical production and light emission were not altered either by xanthine or allopurinol. nor by azide. cyanide or rotenone. The O-2; production increased in the presence of NADH or NADPH. making an NAD(P)H oxidase a likely source. The liberation of reactive oxygen species correlated with the number of leukocytes present in the inflammatory joint fluids. but not with the concentrations of immunoglobulins and complement factor C3.
UR - http://www.scopus.com/inward/record.url?scp=0025257590&partnerID=8YFLogxK
U2 - 10.3109/10715769009087988
DO - 10.3109/10715769009087988
M3 - Journal articles
C2 - 2158476
AN - SCOPUS:0025257590
SN - 1071-5762
VL - 8
SP - 149
EP - 160
JO - Free Radical Research
JF - Free Radical Research
IS - 3
ER -