A SIMPLE RELIABLE ASSAY FOR MYELOPEROXIDASE ACTIVITY IN MIXED NEUTROPHIL-EOSINOPHIL CELL-SUSPENSIONS - APPLICATION TO DETECTION OF MYELOPEROXIDASE DEFICIENCY

被引:43
作者
CRAMER, R
SORANZO, MR
DRI, P
MENEGAZZI, R
PITOTTI, A
ZABUCCHI, G
PATRIARCA, P
机构
[1] UNIV TRIESTE, IST PATOL GEN, I-34127 TRIESTE, ITALY
[2] UNIV TRIESTE, IST TECN & LEGISLAZ FARMACEUT, I-34127 TRIESTE, ITALY
关键词
D O I
10.1016/0022-1759(84)90396-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantitation of myeloperoxidase (MPO) activity by guaiacol peroxidation (GP) assay is profoundly affected by the peroxidase present in [human] eosinophils (EPO) that contaminate the granulocyte suspensions. Inclusion of 3-amino-1,2,4-triazole (AMT) in the GP assay permits quantitation of MPO activity in mixed neutrophil-eosinophil suspensions because of the differential inhibition of EPO and MPO by AMT. The peroxidase activity of eosinophil-free granulocyte suspensions is not appreciably affected by AMT. In the presence of AMT the peroxidase activities of granulocyte preparations containing different numbers of eosinophils are similar on a neutrophil basis, regardless of the number of eosinophils and correspond with the activity of eosinophil-free granulocyte suspensions. AMT almost completely inhibits the activity of partially purified EPO, only slightly affecting the catalytic activity of partially purified MPO. AMT completely inhibits the residual peroxidase activity of granulocyte suspensions from MPO-deficient subjects contributed by contaminating eosinophils. The GP assay in the presence of AMT was used to study the pattern of hereditary transmission of MPO deficiency. The genealogy derived on the basis of this assay was compatible with an autosomal recessive inheritance, in agreement with previously reported results, while no definite pattern of inheritance could be established by use of the GP assay without AMT. The GP assay supplemented with AMT is the method of choice for detection of MPO deficiency, particularly partial deficiency.
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页码:119 / 125
页数:7
相关论文
共 12 条
[1]   SOME ENZYMATIC CHARACTERISTICS OF EOSINOPHIL PEROXIDASE FROM PATIENTS WITH EOSINOPHILIA AND FROM HEALTHY DONORS [J].
BOS, AJ ;
WEVER, R ;
HAMERS, MN ;
ROOS, D .
INFECTION AND IMMUNITY, 1981, 32 (02) :427-431
[2]  
BOS AJ, 1982, J LAB CLIN MED, V99, P589
[3]   ASSAY OF CATALASES AND PEROXIDASES [J].
CHANCE, B ;
MAEHLY, AC .
METHODS IN ENZYMOLOGY, 1955, 2 :764-775
[4]   INCIDENCE OF MYELOPEROXIDASE DEFICIENCY IN AN AREA OF NORTHERN ITALY - HISTOCHEMICAL, BIOCHEMICAL AND FUNCTIONAL-STUDIES [J].
CRAMER, R ;
SORANZO, MR ;
DRI, P ;
ROTTINI, GD ;
BRAMEZZA, M ;
CIRIELLI, S ;
PATRIARCA, P .
BRITISH JOURNAL OF HAEMATOLOGY, 1982, 51 (01) :81-87
[5]  
CRAMER R, 1980, MACROPHAGES LYMPHOCY, P91
[6]  
DRI P, 1982, BLOOD, V60, P323
[7]  
FABIAN I, 1975, J RETICULOENDOTH SOC, V17, P141
[8]   LEUKOCYTE MYELOPEROXIDASE DEFICIENCY AND DISSEMINATED CANDIDIASIS - ROLE OF MYELOPEROXIDASE IN RESISTANCE TO CANDIDA INFECTION [J].
LEHRER, RI ;
CLINE, MJ .
JOURNAL OF CLINICAL INVESTIGATION, 1969, 48 (08) :1478-+
[9]  
MAGE MG, 1971, J RETICULOENDOTH SOC, V9, P201
[10]   HUMAN EOSINOPHILIC PEROXIDASE - BIOCHEMICAL CHARACTERIZATION [J].
MIGLER, R ;
DECHATELET, LR .
BIOCHEMICAL MEDICINE, 1978, 19 (01) :16-26