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Published as doi: 10.1096/fj.07-8534com.
(The FASEB Journal. 2007;21:4059-4069.)
© 2007 FASEB
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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)

Peter Gunnarsson*,1, Louise Levander{dagger}, Peter Påhlsson{dagger} and Magnus Grenegård*

* Division of Pharmacology, Department of Medicine and Care, and

{dagger} Division of Cell Biology, Department of Biomedicine and Surgery, Linköping University, Linköping, Sweden

1Correspondence: Division of Pharmacology, Department of Medicine and Care, Linköping University, S-581 85 Linköping, Sweden. E-mail: petgu{at}imv.liu.se

We studied whether the acute-phase protein {alpha}1-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 µg/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.—Gunnarsson, P., Levander, L., Påhlsson, P., Grenegård, M. 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).


Key Words: orosomucoid • plasma protein • calcium signaling • carbohydrate • L-selectin • phagocyte







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