Effect of Lung Surfactant Collectins on Bronchoalveolar Macrophage Interaction with Blastomyces dermatitidis : Inhibition of Tumor Necrosis Factor Alpha Production by Surfactant Protein D

Author:

Lekkala Madhavi1,LeVine Ann Marie2,Linke Michael J.3,Crouch Erika C.4,Linders Bruce4,Brummer Elmer15,Stevens David A.15

Affiliation:

1. Division of Infectious Diseases, Department of Medicine, Santa Clara Valley Medical Center, and California Institute for Medical Research, San Jose, California

2. Division of Pulmonary Biology and Critical Care Medicine, Children's Hospital Medical Center, Cincinnati, Ohio

3. Veterans Affairs Medical Center, Cincinnati, Ohio

4. Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri

5. Department of Medicine, Stanford University School of Medicine, Stanford, California

Abstract

ABSTRACT Alveolar surfactant modulates the antimicrobial function of bronchoalveolar macrophages (BAM). Little is known about the effect of surfactant-associated proteins in bronchoalveolar lavage fluid (BALF) on the interaction of BAM and Blastomyces dermatitidis . We investigated BALF enhancement or inhibition of TNF-α production by BAM stimulated by B. dermatitidis . BAM from CD-1 mice were stimulated with B. dermatitidis without or with normal BALF, surfactant protein A-deficient (SP-A −/− ) or surfactant protein D-deficient (SP-D −/− ) BALF, or a mixture of SP-A −/− and SP-D −/− BALF. An enzyme-linked immunosorbent assay was used to measure tumor necrosis factor alpha (TNF-α) in culture supernatants. BALFs were standardized in protein concentration. BAM plus B. dermatitidis (BAM- B. dermatitidis ) TNF-α production was inhibited ≥47% by BALF or SP-A −/− BALF (at 290 or 580 μg of protein/ml, P < 0.05 to 0.01); in contrast, SP-D −/− BALF did not significantly inhibit TNF-α production. If SP-A −/− BALF was mixed in equal amounts with SP-D −/− BALF, TNF-α production by BAM- B. dermatitidis was inhibited ( P < 0.01). Finally, pure SP-D added to SP-D −/− BALF inhibited TNF-α production by BAM- B. dermatitidis ( P < 0.01). B. dermatitidis incubated with BALF and washed, plus BAM, stimulated 63% less production of TNF-α than did unwashed B. dermatitidis ( P < 0.05). SP-D was detected by anti-SP-D antibody on BALF-treated unwashed B. dermatitidis in an immunofluorescence assay (IFA). The BALF depleted by a coating of B. dermatitidis lost the ability to inhibit TNF-α production ( P  < 0.05). 1,3-β-Glucan was a good stimulator of BAM for TNF-α production and was detected on B. dermatitidis by IFA. β-Glucan incubated with BALF inhibited the binding of SP-D in BALF to B. dermatitidis as demonstrated by IFA. Our data suggest that SP-D in BALF binds β-glucan on B. dermatitidis , blocking BAM access to β-glucan, thereby inhibiting TNF-α production. Thus, whereas BALF constituents commonly mediate antimicrobial activity, B. dermatitidis may utilize BALF constituents, such as SP-D, to blunt the host defensive reaction; this effect could reduce inflammation and tissue destruction but could also promote disease.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Immunology,Microbiology,Parasitology

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