N-acetyl-beta-D-glucosaminidase (NAG) isoenzymes release from human monocyte-derived macrophages in response to zymosan and human recombinant interferon-gamma

Clin Chim Acta. 1991 Jun 14;199(2):185-94. doi: 10.1016/0009-8981(91)90110-x.

Abstract

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.

MeSH terms

  • Acetylglucosaminidase / isolation & purification
  • Acetylglucosaminidase / metabolism*
  • Humans
  • Interferon-gamma / pharmacology*
  • Isoelectric Focusing
  • Isoenzymes / isolation & purification
  • Isoenzymes / metabolism*
  • Macrophages / drug effects
  • Macrophages / enzymology*
  • Recombinant Proteins
  • Zymosan / pharmacology*

Substances

  • Isoenzymes
  • Recombinant Proteins
  • Interferon-gamma
  • Zymosan
  • Acetylglucosaminidase