Surfactant-associated protein A inhibits LPS-induced cytokine and nitric oxide production in vivo

Am J Physiol Lung Cell Mol Physiol. 2000 Apr;278(4):L840-7. doi: 10.1152/ajplung.2000.278.4.L840.

Abstract

The role of surfactant-associated protein (SP) A in the mediation of pulmonary responses to bacterial lipopolysaccharide (LPS) was assessed in vivo with SP-A gene-targeted [SP-deficient; SP-A(-/-)] and wild-type [SP-A(+/+)] mice. Concentrations of tumor necrosis factor (TNF)-alpha, macrophage inflammatory protein-2, and nitric oxide were determined in recovered bronchoalveolar lavage fluid after intratracheal administration of LPS. SP-A(-/-) mice produced significantly more TNF-alpha and nitric oxide than SP-A(+/+) mice after LPS treatment. Intratracheal administration of human SP-A (1 mg/kg) to SP-A(-/-) mice restored regulation of TNF-alpha, macrophage inflammatory protein-2, and nitric oxide production to that of SP-A(+/+) mice. Other markers of lung injury including bronchoalveolar fluid protein, phospholipid content, and neutrophil numbers were not influenced by SP-A. Data from experiments designed to test possible mechanisms of SP-A-mediated suppression suggest that neither binding of LPS by SP-A nor enhanced LPS clearance are the primary means of inhibition. Our data and others suggest that SP-A acts directly on immune cells to suppress LPS-induced inflammation. These results demonstrate that endogenous or exogenous SP-A inhibits pulmonary LPS-induced cytokine and nitric oxide production in vivo.

Publication types

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

MeSH terms

  • Animals
  • Bronchoalveolar Lavage Fluid / chemistry
  • Chemokine CXCL2
  • Cytokines / antagonists & inhibitors*
  • Cytokines / biosynthesis
  • Escherichia coli
  • Female
  • Humans
  • Lipopolysaccharides / metabolism
  • Lipopolysaccharides / pharmacology*
  • Male
  • Mice
  • Monokines / metabolism
  • Nitric Oxide / antagonists & inhibitors*
  • Nitric Oxide / biosynthesis
  • Nitrites / antagonists & inhibitors
  • Pneumonia / metabolism
  • Proteolipids / metabolism
  • Proteolipids / pharmacology*
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Surfactants / metabolism
  • Pulmonary Surfactants / pharmacology*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors

Substances

  • Chemokine CXCL2
  • Cytokines
  • Lipopolysaccharides
  • Monokines
  • Nitrites
  • Proteolipids
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactant-Associated Proteins
  • Pulmonary Surfactants
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide