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Increased prevalence of low oligomeric state surfactant protein D with restricted lectin activity in bronchoalveolar lavage fluid from preterm infants

Increased prevalence of low oligomeric state surfactant protein D with restricted lectin activity in bronchoalveolar lavage fluid from preterm infants
Increased prevalence of low oligomeric state surfactant protein D with restricted lectin activity in bronchoalveolar lavage fluid from preterm infants
Background: Surfactant protein D (SP-D) is a soluble oligomeric C-type lectin known to protect against lipopolysaccharide and ventilator-induced lung injury in preterm lambs. Here we assess the expression and functional status of SP-D in bronchoalveolar lavage fluid (BALF) from preterm infants at risk of chronic lung disease (CLD) of prematurity and term controls. This is the first systematic evaluation of SP-D function in any clinical cohort.

Methods: SP-D was quantified in BALF from 28 ventilated preterm infants and five ventilated term infants. SP-D lectin activity was tested in a zymosan binding assay followed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and western blot in BALF from the same infants. SP-D lectin activity was also tested towards maltose-agarose and mannan for selected BALF samples.

Results: SP-D expression was lower on day 1 in those preterm infants who subsequently developed CLD but increased over the first 5 days of life in term and preterm neonates. The percentage of neonatal SP-D capable of binding zymosan rarely exceeded 50% in any BALF sample and was 3.5 times lower in preterm infants than term infants on day 1 of life. Similar binding defects were observed towards maltose-agarose and mannan. SDS-PAGE analysis revealed that zymosan-bound SP-D was more highly oligomerised (?12-mers) than unbound SP-D, which was composed primarily of trimers and lower oligomeric forms.

Conclusions: Substantial and functionally relevant variation in the expression and oligomeric distribution of SP-D exists between preterm and term neonatal lung secretions. This has implications for proposed SP-D replacement therapy in this population.
0040-6376
460-467
Kotecha, Sailesh
407c1de7-7151-4e19-95a9-66f3111d483a
Davies, Philip L.
cb114577-3f27-436c-be75-f434d388d534
Clark, Howard W.
70550b6d-3bd7-47c6-8c02-4f43f37d5213
McGreal, Eamon P.
6ca021ea-09c4-4f08-888f-e82330d7a413
Kotecha, Sailesh
407c1de7-7151-4e19-95a9-66f3111d483a
Davies, Philip L.
cb114577-3f27-436c-be75-f434d388d534
Clark, Howard W.
70550b6d-3bd7-47c6-8c02-4f43f37d5213
McGreal, Eamon P.
6ca021ea-09c4-4f08-888f-e82330d7a413

Kotecha, Sailesh, Davies, Philip L., Clark, Howard W. and McGreal, Eamon P. (2013) Increased prevalence of low oligomeric state surfactant protein D with restricted lectin activity in bronchoalveolar lavage fluid from preterm infants. Thorax, 68 (5), 460-467. (doi:10.1136/thoraxjnl-2012-202729). (PMID:23390139)

Record type: Article

Abstract

Background: Surfactant protein D (SP-D) is a soluble oligomeric C-type lectin known to protect against lipopolysaccharide and ventilator-induced lung injury in preterm lambs. Here we assess the expression and functional status of SP-D in bronchoalveolar lavage fluid (BALF) from preterm infants at risk of chronic lung disease (CLD) of prematurity and term controls. This is the first systematic evaluation of SP-D function in any clinical cohort.

Methods: SP-D was quantified in BALF from 28 ventilated preterm infants and five ventilated term infants. SP-D lectin activity was tested in a zymosan binding assay followed by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and western blot in BALF from the same infants. SP-D lectin activity was also tested towards maltose-agarose and mannan for selected BALF samples.

Results: SP-D expression was lower on day 1 in those preterm infants who subsequently developed CLD but increased over the first 5 days of life in term and preterm neonates. The percentage of neonatal SP-D capable of binding zymosan rarely exceeded 50% in any BALF sample and was 3.5 times lower in preterm infants than term infants on day 1 of life. Similar binding defects were observed towards maltose-agarose and mannan. SDS-PAGE analysis revealed that zymosan-bound SP-D was more highly oligomerised (?12-mers) than unbound SP-D, which was composed primarily of trimers and lower oligomeric forms.

Conclusions: Substantial and functionally relevant variation in the expression and oligomeric distribution of SP-D exists between preterm and term neonatal lung secretions. This has implications for proposed SP-D replacement therapy in this population.

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Published date: May 2013
Organisations: Clinical & Experimental Sciences

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Local EPrints ID: 351213
URI: http://eprints.soton.ac.uk/id/eprint/351213
ISSN: 0040-6376
PURE UUID: c10bd7e8-40f0-44d3-bd53-13d1df916b98

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Date deposited: 17 Apr 2013 11:53
Last modified: 14 Mar 2024 13:36

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Contributors

Author: Sailesh Kotecha
Author: Philip L. Davies
Author: Howard W. Clark
Author: Eamon P. McGreal

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