Production of oxygen radicals by fibroblasts and neutrophils from a patient with x‐linked chronic granulomatous disease

Abstract: Recently, a superoxide‐generating NADPH‐oxidase system in human fibroblasts has been described. Therefore, we reassessed the possible use of this cell type for prenatal diagnosis of CGD patients comparing normal and CGD peripheral blood neutrophils (PMN) and skin fibroblasts in their reactive oxygen intermediate (ROI)‐producing capacity. While PMN of the CGD patient showed a clearly reduced respiratory burst activity, which correlated well with the measured content of cytochrome b558, fibroblasts of the same individual showed no impaired production of superoxide anion or H2O2 upon stimulation by cytokines (TNF and IL‐1) or other agents (Ca2+ ionophores and PAF, unpublished results). Furthermore, fibroblasts of the CGD patient or of normal donors could be inhibited in ROI production by diphenylene iodonium (DPI) and 2‐iodobiphenyl. In contrast to PMN, no inhibition of the fibroblast NADPH‐oxidase system was observed using staurosporin, an inhibitor of proteinkinase C. These data demonstrate, in contrast to previous studies, that fibroblasts are able to produce ROI. Nevertheless, since fibroblasts obtained from a CGD patient exhibited no difference in ROI production compared with fibroblasts obtained from healthy donors, they are not suitable for prenatal diagnosis of CGD.

[1]  A. Jesaitis,et al.  The cytochrome b-558 molecules involved in the fibroblast and polymorphonuclear leucocyte superoxide-generating NADPH oxidase systems are structurally and genetically distinct. , 1993, Biochemical Journal.

[2]  J. Hancock,et al.  Functional expression of NADPH oxidase components (alpha- and beta-subunits of cytochrome b558 and 45-kDa flavoprotein) by intrinsic human glomerular mesangial cells. , 1991, The Journal of biological chemistry.

[3]  P. Baeuerle,et al.  A role for oxygen radicals as second messengers. , 1991, Trends in cell biology.

[4]  G. Rothe,et al.  Flow cytometric measurement of the respiratory burst activity of phagocytes using dihydrorhodamine 123. , 1991, Journal of immunological methods.

[5]  A R Cross,et al.  Identification of a superoxide-generating NADPH oxidase system in human fibroblasts. , 1991, The Biochemical journal.

[6]  J. Curnutte,et al.  Molecular basis of chronic granulomatous disease [see comments] , 1991 .

[7]  R. M. Smith,et al.  Molecular basis of chronic granulomatous disease. , 1991, Blood.

[8]  G. Habermehl,et al.  Human fibroblasts release low amounts of reactive oxygen species in response to the potent phagocyte stimulants, serum-treated zymosan, N-formyl-methionyl-leucyl-phenylalanine, leukotriene B4 or 12-O-tetradecanoylphorbol 13-acetate. , 1990, Biological chemistry Hoppe-Seyler.

[9]  M. Lohmann‐Matthes,et al.  A fast and easy method to determine the production of reactive oxygen intermediates by human and murine phagocytes using dihydrorhodamine 123. , 1990, Journal of immunological methods.

[10]  G. Habermehl,et al.  Human fibroblasts release reactive oxygen species in response to interleukin-1 or tumour necrosis factor-alpha. , 1989, The Biochemical journal.

[11]  D. Roos,et al.  Immunocytochemical discovery of the 22- to 23-Kd subunit of cytochrome b558 at the surface of human peripheral phagocytes. , 1988, Blood.

[12]  A. Segal Absence of both cytochrome b−245 subunits from neutrophils in X-linked chronic granulomatous disease , 1987, Nature.

[13]  D. Wara,et al.  Prenatal diagnosis of chronic granulomatous disease. , 1984, American journal of medical genetics.

[14]  R. Seger,et al.  PRENATAL DIAGNOSIS OF CHRONIC GRANULOMATOUS DISEASE: UNRELIABILITY OF FIBROBLAST NITROBLUE TETRAZOLIUM TEST , 1981, The Lancet.

[15]  R. Good,et al.  FIBROBLAST NITROBLUE TETRAZOLIUM TEST AND THE IN-UTERO DIAGNOSIS OF CHRONIC GRANULOMATOUS DISEASE , 1980, The Lancet.

[16]  B. Babior,et al.  Defective superoxide production by granulocytes from patients with chronic granulomatous disease. , 1974, The New England journal of medicine.

[17]  L. Flohé,et al.  Respiratory chain linked H2O2 production in pigeon heart mitochondria , 1971, FEBS letters.

[18]  I. Fridovich,et al.  Superoxide dismutase. An enzymic function for erythrocuprein (hemocuprein). , 1969, The Journal of biological chemistry.

[19]  R. B. Sandin,et al.  Synthesis of Some Cyclic Iodonium Salts , 1956 .

[20]  Tyler K. Nygaard,et al.  Phagocytes , 1891, The Indian medical gazette.