B. Otto et A. Ogilvie, THE RESPONSE OF PERITONEAL-MACROPHAGES AFTER IMPLANTATION OF SEVERAL CERAMICS AS MEASURED BY THE CHANGE OF ECTOENZYME ACTIVITY, Biomaterials, 19(11-12), 1998, pp. 1049-1055
The bioactive calcium phosphate ceramics with various calcium:phosphor
us ratios: Ca/P = 1.67 (hydroxyapatite, HA), Ca/P = 1.6 and Ca/P = 1.5
(tricalcium phosphate, beta-TCP), the bioinert aluminium oxide cerami
c (Al2O3) and the toxic calcium oxide ceramic (CaO) have been investig
ated with respect to their ability to activate peritoneal macrophages
of NMRI-mice and with respect to their influence on the extracellular
nucleotide degradation of these macrophages. Two weeks after the intra
peritoneal injection of a suspension of ceramic particles in an isoton
e salt solution (phosphate-buffered saline = PBS), we observed that th
e peritoneal macrophages were only slightly activated into the respons
ive state, independent of the type of ceramic. 5'Nucleotidase (5'N) ec
toenzyme hydrolyses adenosine monophosphate (AMP) and a decrease of it
s activity is a general biochemical marker of activated macrophages. T
his ectoenzyme activity was slightly reduced after ceramic implantatio
n. The lacking rise of the extracellular diadenosine tetraphosphate (A
p(4)A)-catabolism by the macrophage ectoenzyme alkaline phosphodiester
ase I (APD) demonstrated that the peritoneal macrophages did not compl
etely reach the responsive state. After the implantation of calcium ph
osphate ceramics the extracellular adenosine triphosphate (ATP)-reduct
ion was slightly diminished. After the implantation of tricalcium phos
phate ceramic about 30% more peritoneal exsudate cells (PEC) were obta
ined from the peritoneal cavity than after injections of pure PBS (use
d as non-inflammatory control). Similar to the phenomena following the
injection of thioglycollate (Tg, inflammation producing control agent
) a slightly but not significantly increased proportion of pseudopodia
-building cells was observed after the implantation of the ceramic wit
h Ca/P = 1.6. (C) 1998 Published by Elsevier Science Ltd. All rights r
eserved.