N-ACETYL-BETA-D-GLUCOSAMINIDASE (NAG) ISOENZYMES RELEASE FROM HUMAN MONOCYTE-DERIVED MACROPHAGES IN RESPONSE TO ZYMOSAN AND HUMAN RECOMBINANT INTERFERON-GAMMA
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BOURBOUZE, R
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UNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCEUNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCE
BOURBOUZE, R
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RAFFI, F
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UNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCEUNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCE
RAFFI, F
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DAMERON, G
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UNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCEUNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCE
DAMERON, G
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HALIMIRAFTAB, H
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UNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCEUNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCE
HALIMIRAFTAB, H
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LOKO, F
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UNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCEUNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCE
LOKO, F
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VILDE, JL
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UNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCEUNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCE
VILDE, JL
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[1] UNIV PARIS 07,HOP BICHAT CLAUDE BERNARD,INSERM,U13,F-75221 PARIS 05,FRANCE
Secretion of N-acetyl-beta-D-glucosaminidase (NAG) isoenzymes by human blood monocyte-derived macrophages in response to zymosan and human recombinant interferon-gamma was studied. Macrophages were found to release NAG in response to zymosan, but interferon-gamma has no effect on secretion. Isoenzyme separation by isoelectric focusing demonstrates that non stimulated and zymosan or interferon-gamma treated macrophages release predominantly NAG B and, to a lesser extent, NAG A isoenzymes. In all these conditions, the intracellular intermediate form NAG I could not be detected in the media. Thus, activated macrophages may not be the source of NAG intermediate forms I and P in pathological or maternal serum. In contrast, macrophages could contribute to a significant elevation of urinary activity and NAG B excretion in response to inflammatory conditions.