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Review
. 2000;1(2):93-108.
doi: 10.1186/rr19. Epub 2000 Aug 25.

Surfactant protein-D and pulmonary host defense

Affiliations
Review

Surfactant protein-D and pulmonary host defense

E C Crouch. Respir Res. 2000.

Abstract

Surfactant protein-D (SP-D) participates in the innate response to inhaled microorganisms and organic antigens, and contributes to immune and inflammatory regulation within the lung. SP-D is synthesized and secreted by alveolar and bronchiolar epithelial cells, but is also expressed by epithelial cells lining various exocrine ducts and the mucosa of the gastrointestinal and genitourinary tracts. SP-D, a collagenous calcium-dependent lectin (or collectin), binds to surface glycoconjugates expressed by a wide variety of microorganisms, and to oligosaccharides associated with the surface of various complex organic antigens. SP-D also specifically interacts with glycoconjugates and other molecules expressed on the surface of macrophages, neutrophils, and lymphocytes. In addition, SP-D binds to specific surfactant-associated lipids and can influence the organization of lipid mixtures containing phosphatidylinositol in vitro. Consistent with these diverse in vitro activities is the observation that SP-D-deficient transgenic mice show abnormal accumulations of surfactant lipids, and respond abnormally to challenge with respiratory viruses and bacterial lipopolysaccharides. The phenotype of macrophages isolated from the lungs of SP-D-deficient mice is altered, and there is circumstantial evidence that abnormal oxidant metabolism and/or increased metalloproteinase expression contributes to the development of emphysema. The expression of SP-D is increased in response to many forms of lung injury, and deficient accumulation of appropriately oligomerized SP-D might contribute to the pathogenesis of a variety of human lung diseases.

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Figures

Figure 1
Figure 1
Molecular structure of SP-D. (a) Schematic diagram illustrating the structure of SP-D dodecamers, which consist of four trimeric subunits, and SP-D trimers. (b) Quick-freeze deep-etch image of human SP-D dodecamers, SP-D multimers, and the SP-D binding protein gp-340 (kindly provided by John Heuser, Washington University School of Medicine, St Louis, Missouri, USA).

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