Hm. Burt et Jk. Jackson, ENHANCEMENT OF CRYSTAL-INDUCED NEUTROPHIL RESPONSES BY OPSONIZATION OF CALCIUM PYROPHOSPHATE DIHYDRATE CRYSTALS, Annals of the Rheumatic Diseases, 52(8), 1993, pp. 599-607
Objectives-Little is known about the effect on crystal induced neutrop
hil responses of the opsonisation of calcium pyrophosphate dihydrate (
CPPD) (triclinic) crystals with components of serum and plasma. The pu
rpose of this study was to determine the effects of precoating CPPD cr
ystals with plasma, serum, complement depleted serum, and IgG on a ful
l range of crystal induced neutrophil responses (calcium mobilisation,
chemiluminescence, superoxide anion production, non-cytolytic lysosom
al enzyme release, and leukotriene synthesis). Methods-Crystals were p
recoated with IgG, serum, plasma, or complement depleted serum (heated
at 56-degrees-C), incubated with neutrophils and the responses monito
red with time. Measurement of the extent of neutrophil association wit
h crystals was based on monitoring the decrease in fluorescence intens
ity of supernatants when crystals and diphenyl-hexatriene labelled neu
trophils were allowed to settle under gravity. Results-Precoating CPPD
crystals with IgG, plasma, and serum significantly enhanced chemilumi
nescence, superoxide anion generation, increases in cytosolic free cal
cium levels, and non-cytolytic lysosomal enzyme release by neutrophils
compared with uncoated CPPD crystals. The enhancement of neutrophil r
esponses by crystals coated with complement depleted serum was less pr
onounced. The increased neutrophil responses induced by CPPD crystals
coated with IgG might have been due to the observed increase in the as
sociation of IgG coated crystals with neutrophils. Conclusions-These d
ata show that there is a marked potentiation of all neutrophil respons
es to IgG, plasma, and serum coated CPPD crystals. It is suggested tha
t the adsorption of synovial fluid proteins, including IgG and C3b, to
CPPD crystals in vivo, results in the opsonised crystals becoming a p
otent neutrophil stimulant and inflammatory agent,