The acute-phase protein alpha 1-acid glycoprotein (AGP) induces rises in cytosolic Ca2+ in neutrophil granulocytes via sialic acid binding immunoglobulin-like lectins (siglecs)

FASEB J. 2007 Dec;21(14):4059-69. doi: 10.1096/fj.07-8534com. Epub 2007 Aug 3.

Abstract

We studied whether the acute-phase protein alpha1-acid glycoprotein (AGP) induces rises in [Ca2+]i in neutrophils and sought to identify the corresponding AGP receptor (or receptors). We found that AGP elicited a minimal rise in [Ca2+]i in Fura-2-loaded neutrophils, and this response was markedly enhanced by pretreatment with anti-L-selectin antibodies. (The EC50 value of the AGP-induced Ca2+ response was 9 microg/ml.) Activation of phospholipase-C, Src tyrosine kinases, and PI3 kinases proved to be essential for the AGP-mediated increase in [Ca2+]i, whereas the p38 MAPK and SYK signaling pathways were not involved. Furthermore, antibodies against sialic acid binding, immunoglobulin-like lectin 5 (Siglec-5) and oligosaccharide 3'-sialyl-lactose both antagonized the AGP-induced response and caused an immediate increase in [Ca2+]i in anti-L-selectin-treated neutrophils, which indicates a signaling capacity of Siglec-5. We used modified forms of AGP (treated with mild periodate or neuraminidase) to establish the importance of sialic acid residues. The modified forms of AGP caused a much smaller rise in [Ca2+]i than did unaltered AGP. Affinity chromatography confirmed that unchanged AGP, but not neuraminidase-treated AGP, bound to Siglec-5. Our report provides the first evidence for a signaling capacity by AGP through a defined receptor. Pre-engagement of L-selectin significantly enhanced this signaling capacity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / metabolism
  • Antigens, Differentiation, Myelomonocytic / metabolism
  • Calcium / metabolism*
  • Cations, Divalent / metabolism
  • Cells, Cultured
  • Cytosol / metabolism*
  • HL-60 Cells
  • Humans
  • Lectins / metabolism
  • Lectins / physiology*
  • Ligands
  • N-Acetylneuraminic Acid / metabolism*
  • Neutrophils / metabolism*
  • Orosomucoid / metabolism
  • Orosomucoid / physiology*
  • Sialic Acid Binding Immunoglobulin-like Lectins

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Cations, Divalent
  • Lectins
  • Ligands
  • Orosomucoid
  • SIGLEC5 protein, human
  • Sialic Acid Binding Immunoglobulin-like Lectins
  • N-Acetylneuraminic Acid
  • Calcium