<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ding PH</submitter><funding>The Hong Kong Research Grants Council</funding><funding>The University of Hong Kong (HKU)</funding><pagination>e0173223</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5383028</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(4)</volume><pubmed_abstract>Lipopolysaccharide (LPS)-binding protein (LBP) as an acute-phase protein plays a crucial role in innate host response to bacterial challenge. Our previous study shows that LBP expression in human gingiva is associated with periodontal status. Porphyromonas gingivalis is a keystone periodontopathogen, and its LPS with lipid A structural heterogeneity critically accounts for periodontal pathogenesis. This study investigated the effects of LBP and its interactions with two featured isoforms of P. gingivalis LPS (tetra-acylated LPS1435/1449 and penta-acylated LPS1690) on the expression of pro-inflammatory cytokines in human oral keratinocytes (HOKs), and the involvement of Toll-like receptor (TLR) signaling. HOKs were pre-incubated with recombinant human LBP (rhLBP) at 10ng/ml, 100ng/ml and 1μ</pubmed_abstract><journal>PloS one</journal><pubmed_title>3LPS-binding protein and its interactions with P. gingivalis LPS modulate pro-inflammatory response and Toll-like receptor signaling in human oral keratinocytes.</pubmed_title><pmcid>PMC5383028</pmcid><funding_grant_id>GRF 768411M, 768713M and 17155216</funding_grant_id><funding_grant_id>The Modern Dental Laboratory/HKU Endowment Fund</funding_grant_id><pubmed_authors>Wang CY</pubmed_authors><pubmed_authors>Ding PH</pubmed_authors><pubmed_authors>Darveau RP</pubmed_authors><pubmed_authors>Jin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>3LPS-binding protein and its interactions with P. gingivalis LPS modulate pro-inflammatory response and Toll-like receptor signaling in human oral keratinocytes.</name><description>Lipopolysaccharide (LPS)-binding protein (LBP) as an acute-phase protein plays a crucial role in innate host response to bacterial challenge. Our previous study shows that LBP expression in human gingiva is associated with periodontal status. Porphyromonas gingivalis is a keystone periodontopathogen, and its LPS with lipid A structural heterogeneity critically accounts for periodontal pathogenesis. This study investigated the effects of LBP and its interactions with two featured isoforms of P. gingivalis LPS (tetra-acylated LPS1435/1449 and penta-acylated LPS1690) on the expression of pro-inflammatory cytokines in human oral keratinocytes (HOKs), and the involvement of Toll-like receptor (TLR) signaling. HOKs were pre-incubated with recombinant human LBP (rhLBP) at 10ng/ml, 100ng/ml and 1μ</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017</publication><modification>2025-04-26T11:11:04.239Z</modification><creation>2019-06-06T17:17:11Z</creation></dates><accession>S-EPMC5383028</accession><cross_references><pubmed>28384159</pubmed><doi>10.1371/journal.pone.0173223</doi></cross_references></HashMap>