<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(12)</volume><submitter>Chakraborty M</submitter><pubmed_abstract>&lt;h4>Rationale&lt;/h4>The chemokine interleukin-8 is implicated in the development of bronchopulmonary dysplasia in preterm infants. The 77-amino acid isoform of interleukin-8 (interleukin-877) is a less potent chemoattractant than other shorter isoforms. Although interleukin-877 is abundant in the preterm circulation, its regulation in the preterm lung is unknown.&lt;h4>Objectives&lt;/h4>To study expression and processing of pulmonary interleukin-877 in preterm infants who did and did not develop bronchopulmonary dysplasia.&lt;h4>Methods&lt;/h4>Total interleukin-8 and interleukin-877 were measured in bronchoalveolar lavage fluid from preterm infants by immunoassay. Neutrophil serine proteases were used to assess processing. Neutrophil chemotaxis assays and degranulation of neutrophil matrix metalloprotei</pubmed_abstract><journal>PloS one</journal><pagination>e114524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4256433</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Role of serine proteases in the regulation of interleukin-877 during the development of bronchopulmonary dysplasia in preterm ventilated infants.</pubmed_title><pmcid>PMC4256433</pmcid><pubmed_authors>Powell W</pubmed_authors><pubmed_authors>Davies PL</pubmed_authors><pubmed_authors>Hogwood J</pubmed_authors><pubmed_authors>Gray E</pubmed_authors><pubmed_authors>McGreal EP</pubmed_authors><pubmed_authors>Spiller B</pubmed_authors><pubmed_authors>Kotecha S</pubmed_authors><pubmed_authors>Voitenok NN</pubmed_authors><pubmed_authors>Chambers RC</pubmed_authors><pubmed_authors>Williams A</pubmed_authors><pubmed_authors>Chakraborty M</pubmed_authors><pubmed_authors>Abdulla S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Role of serine proteases in the regulation of interleukin-877 during the development of bronchopulmonary dysplasia in preterm ventilated infants.</name><description>&lt;h4>Rationale&lt;/h4>The chemokine interleukin-8 is implicated in the development of bronchopulmonary dysplasia in preterm infants. The 77-amino acid isoform of interleukin-8 (interleukin-877) is a less potent chemoattractant than other shorter isoforms. Although interleukin-877 is abundant in the preterm circulation, its regulation in the preterm lung is unknown.&lt;h4>Objectives&lt;/h4>To study expression and processing of pulmonary interleukin-877 in preterm infants who did and did not develop bronchopulmonary dysplasia.&lt;h4>Methods&lt;/h4>Total interleukin-8 and interleukin-877 were measured in bronchoalveolar lavage fluid from preterm infants by immunoassay. Neutrophil serine proteases were used to assess processing. Neutrophil chemotaxis assays and degranulation of neutrophil matrix metalloprotei</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014</publication><modification>2026-07-16T07:27:20.399Z</modification><creation>2019-03-26T23:25:08Z</creation></dates><accession>S-EPMC4256433</accession><cross_references><pubmed>25474412</pubmed><doi>10.1371/journal.pone.0114524</doi></cross_references></HashMap>