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Functional heterogeneity of pulmonary surfactant protein-D in cystic fibrosis

Functional heterogeneity of pulmonary surfactant protein-D in cystic fibrosis
Functional heterogeneity of pulmonary surfactant protein-D in cystic fibrosis
Pulmonary surfactant protein-D (SP-D) is a soluble collagenous C-type lectin with important anti-microbial and anti-inflammatory properties. Although it is subject to functionally relevant modification by common polymorphisms and unregulated inflammation, the functional status of SP-D in cystic fibrosis (CF) remains unclear. Given the importance of infection and inflammation in CF lung pathology we have undertaken the first systematic analysis of SP-D lectin activity in this population. By ELISA, we found that airway lavage fluid SP-D expression was greater in CF compared to control patients but was reduced in CF patients with infection and correlated negatively with markers of neutrophilic inflammation. In a functional assay, the percentage of SP-D capable of binding zymosan rarely exceeded 60% in CF or control patients and similarly restricted binding activity was observed towards maltose–agarose. SP-D lectin activity also correlated negatively with infection and neutrophilic inflammation but there was little evidence of major proteolytic degradation amongst the non-bound material. SP-D which failed to bind zymosan exhibited features of lower oligomeric form compared to bound material when tested by native gel electrophoresis. Furthermore, when separated by gel chromatography, high and low oligomeric populations of SP-D were observed in CF lavage fluid but only high oligomeric forms exhibited substantial lectin activity towards yeast derived mannan. Our data demonstrate that oligomeric heterogeneity underlies functional diversity amongst SP-D in health and disease and that dynamic regulation of oligomerisation is an important feature of SP-D biology.

cystic fibrosis, innate immunity, lung, surfactant protein-D, lectin, inflammation
0006-3002
2391-2400
Kotecha, S.
70a05a14-600a-4beb-8e06-1005fe60db79
Doull, I.
2ec63854-1b37-4577-8c41-54e32b25a4a3
Davies, P.
d09af49a-5bc9-4ce6-b0de-c861fa259fa8
McKenzie, Z.
698469ca-d5f0-42f8-858d-53240903f89d
Madsen, J.
b5d8ae35-00ac-4d19-930e-d8ddec497359
Clark, H.W.
70550b6d-3bd7-47c6-8c02-4f43f37d5213
McGreal, E.P.
bc76d71f-a883-43a8-87d9-99ddc9f1c114
Kotecha, S.
70a05a14-600a-4beb-8e06-1005fe60db79
Doull, I.
2ec63854-1b37-4577-8c41-54e32b25a4a3
Davies, P.
d09af49a-5bc9-4ce6-b0de-c861fa259fa8
McKenzie, Z.
698469ca-d5f0-42f8-858d-53240903f89d
Madsen, J.
b5d8ae35-00ac-4d19-930e-d8ddec497359
Clark, H.W.
70550b6d-3bd7-47c6-8c02-4f43f37d5213
McGreal, E.P.
bc76d71f-a883-43a8-87d9-99ddc9f1c114

Kotecha, S., Doull, I., Davies, P., McKenzie, Z., Madsen, J., Clark, H.W. and McGreal, E.P. (2013) Functional heterogeneity of pulmonary surfactant protein-D in cystic fibrosis. Biochimica et Biophysica Acta, 1832 (12), 2391-2400. (doi:10.1016/j.bbadis.2013.10.002). (PMID:24120837)

Record type: Article

Abstract

Pulmonary surfactant protein-D (SP-D) is a soluble collagenous C-type lectin with important anti-microbial and anti-inflammatory properties. Although it is subject to functionally relevant modification by common polymorphisms and unregulated inflammation, the functional status of SP-D in cystic fibrosis (CF) remains unclear. Given the importance of infection and inflammation in CF lung pathology we have undertaken the first systematic analysis of SP-D lectin activity in this population. By ELISA, we found that airway lavage fluid SP-D expression was greater in CF compared to control patients but was reduced in CF patients with infection and correlated negatively with markers of neutrophilic inflammation. In a functional assay, the percentage of SP-D capable of binding zymosan rarely exceeded 60% in CF or control patients and similarly restricted binding activity was observed towards maltose–agarose. SP-D lectin activity also correlated negatively with infection and neutrophilic inflammation but there was little evidence of major proteolytic degradation amongst the non-bound material. SP-D which failed to bind zymosan exhibited features of lower oligomeric form compared to bound material when tested by native gel electrophoresis. Furthermore, when separated by gel chromatography, high and low oligomeric populations of SP-D were observed in CF lavage fluid but only high oligomeric forms exhibited substantial lectin activity towards yeast derived mannan. Our data demonstrate that oligomeric heterogeneity underlies functional diversity amongst SP-D in health and disease and that dynamic regulation of oligomerisation is an important feature of SP-D biology.

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More information

Published date: 9 October 2013
Keywords: cystic fibrosis, innate immunity, lung, surfactant protein-D, lectin, inflammation
Organisations: Clinical & Experimental Sciences

Identifiers

Local EPrints ID: 359466
URI: http://eprints.soton.ac.uk/id/eprint/359466
ISSN: 0006-3002
PURE UUID: ba3dd062-90f1-4096-af90-5919750f7559
ORCID for J. Madsen: ORCID iD orcid.org/0000-0003-1664-7645

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Date deposited: 04 Nov 2013 11:24
Last modified: 15 Mar 2024 03:29

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Contributors

Author: S. Kotecha
Author: I. Doull
Author: P. Davies
Author: Z. McKenzie
Author: J. Madsen ORCID iD
Author: H.W. Clark
Author: E.P. McGreal

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