Pulmonary surfactant protein A activates a phosphatidylinositol 3-kinase/calcium signal transduction pathway in human macrophages: participation in the up-regulation of mannose receptor activity

J Immunol. 2005 Aug 15;175(4):2227-36. doi: 10.4049/jimmunol.175.4.2227.

Abstract

Surfactant protein A (SP-A), a major component of lung surfactant, binds to macrophages and has been shown to alter several macrophage biological functions, including up-regulation of macrophage mannose receptor (MR) activity. In the present study, we show that SP-A induces signal transduction pathway(s) that impact on MR expression. The addition of human, rat, or recombinant rat SP-A to human monocyte-derived macrophages significantly raised the level of cytosolic Ca2+ above baseline within 10 s of SP-A addition, as measured by spectrofluorometric analysis. SP-A induced a refractory state specific for SP-A consistent with homologous desensitization of a receptor(s) linked to calcium mobilization because a second application of SP-A did not induce a rise in cytosolic Ca2+ whereas the addition of platelet-activating factor did. Using site-directed mutations in SP-A, we determined that both the attached sugars and the collagen-like domain of SP-A are necessary to optimize Ca2+ mobilization. SP-A triggered the increase in cytosolic Ca2+ by inducing activation of phospholipase C, which leads to the hydrolysis of membrane phospholipids, yielding inositol 1,4,5-trisphosphate and mobilizing intracellularly stored Ca2+ by inositol triphosphate-sensitive channels. Finally, inhibition of PI3Ks, which appear to act upstream of phospholipase C in Ca2+ mobilization, decreased the SP-A-induced rise in MR expression, providing evidence that SP-A induction of MR activity involves the activation of a pathway in which PI3K is a component. These studies provide further evidence that SP-A produced in the lung plays a role in modulating macrophage biology, thereby contributing to the alternative activation state of the alveolar macrophage.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Animals
  • Binding Sites / immunology
  • Calcium / metabolism
  • Calcium Signaling / genetics
  • Calcium Signaling / immunology*
  • Collagen / physiology
  • Cytosol / metabolism
  • Dose-Response Relationship, Immunologic
  • Humans
  • Inositol 1,4,5-Trisphosphate / metabolism
  • Inositol 1,4,5-Trisphosphate / physiology
  • Intracellular Fluid / metabolism
  • Lectins, C-Type / biosynthesis*
  • Lectins, C-Type / metabolism
  • Lipopolysaccharides / pharmacology
  • Macrophage Activation / genetics
  • Macrophage Activation / immunology
  • Macrophages / enzymology*
  • Macrophages / metabolism
  • Mannose Receptor
  • Mannose-Binding Lectins / biosynthesis*
  • Mannose-Binding Lectins / metabolism
  • Monocytes / enzymology
  • Monocytes / immunology
  • Monocytes / metabolism
  • Oligosaccharides / physiology
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphatidylinositol 3-Kinases / physiology
  • Protein Structure, Tertiary / physiology
  • Pulmonary Surfactant-Associated Protein A / genetics
  • Pulmonary Surfactant-Associated Protein A / pharmacology
  • Pulmonary Surfactant-Associated Protein A / physiology*
  • Rats
  • Receptors, Cell Surface / biosynthesis*
  • Receptors, Cell Surface / metabolism
  • U937 Cells
  • Up-Regulation / genetics
  • Up-Regulation / immunology*

Substances

  • Lectins, C-Type
  • Lipopolysaccharides
  • Mannose Receptor
  • Mannose-Binding Lectins
  • Oligosaccharides
  • Pulmonary Surfactant-Associated Protein A
  • Receptors, Cell Surface
  • Inositol 1,4,5-Trisphosphate
  • Collagen
  • Calcium