Matches in SemOpenAlex for { <https://semopenalex.org/work/W2108678003> ?p ?o ?g. }
- W2108678003 endingPage "F432" @default.
- W2108678003 startingPage "F421" @default.
- W2108678003 abstract "Serum IL-6 is increased in acute kidney injury (AKI) and inhibition of IL-6 reduces AKI-mediated lung inflammation. We hypothesized that circulating monocytes produce IL-6 and that alveolar macrophages mediate lung inflammation after AKI via chemokine (CXCL1) production. To investigate systemic and alveolar macrophages in lung injury after AKI, sham operation or 22 min of renal pedicle clamping (AKI) was performed in three experimental settings: 1) systemic macrophage depletion via diphtheria toxin (DT) injection to CD11b-DTR transgenic mice, 2) DT injection to wild-type mice, and 3) alveolar macrophage depletion via intratracheal (IT) liposome-encapsulated clodronate (LEC) administration to wild-type mice. In mice with AKI and systemic macrophage depletion (CD11b-DTR transgenic administered DT) vs. vehicle-treated AKI, blood monocytes and lung interstitial macrophages were reduced, renal function was similar, serum IL-6 was increased, lung inflammation was improved, lung CXCL1 was reduced, and lung capillary leak was increased. In wild-type mice with AKI administered DT vs. vehicle, serum IL-6 was increased. In mice with AKI and alveolar macrophage depletion (IT-LEC) vs. AKI with normal alveolar macrophage content, blood monocytes and lung interstitial macrophages were similar, alveolar macrophages were reduced, renal function was similar, lung inflammation was improved, lung CXCL1 was reduced, and lung capillary leak was increased. In conclusion, administration of DT in AKI is proinflammatory, limiting the use of the DTR-transgenic model to study systemic effects of AKI. Mice with AKI and either systemic mononuclear phagocyte depletion or alveolar macrophage depletion had reduced lung inflammation and lung CXCL1, but increased lung capillary leak; thus, mononuclear phagocytes mediate lung inflammation, but they protect against lung capillary leak after ischemic AKI. Since macrophage activation and chemokine production are key events in the development of acute lung injury (ALI), these data provide further evidence that AKI may cause ALI." @default.
- W2108678003 created "2016-06-24" @default.
- W2108678003 creator A5020999347 @default.
- W2108678003 creator A5026436514 @default.
- W2108678003 creator A5035032820 @default.
- W2108678003 creator A5036727605 @default.
- W2108678003 creator A5046679319 @default.
- W2108678003 creator A5058360551 @default.
- W2108678003 creator A5072402432 @default.
- W2108678003 creator A5074044567 @default.
- W2108678003 creator A5076869715 @default.
- W2108678003 creator A5080064369 @default.
- W2108678003 date "2012-02-15" @default.
- W2108678003 modified "2023-10-17" @default.
- W2108678003 title "Macrophages mediate lung inflammation in a mouse model of ischemic acute kidney injury" @default.
- W2108678003 cites W1502093553 @default.
- W2108678003 cites W1739353754 @default.
- W2108678003 cites W1967237457 @default.
- W2108678003 cites W1977631233 @default.
- W2108678003 cites W1995403745 @default.
- W2108678003 cites W1997653917 @default.
- W2108678003 cites W1998497949 @default.
- W2108678003 cites W2006303725 @default.
- W2108678003 cites W2008912014 @default.
- W2108678003 cites W2025821558 @default.
- W2108678003 cites W2029723446 @default.
- W2108678003 cites W2037258934 @default.
- W2108678003 cites W2043132544 @default.
- W2108678003 cites W2048519644 @default.
- W2108678003 cites W2051338691 @default.
- W2108678003 cites W2054451736 @default.
- W2108678003 cites W2055817721 @default.
- W2108678003 cites W2056699935 @default.
- W2108678003 cites W2068223929 @default.
- W2108678003 cites W2079441648 @default.
- W2108678003 cites W2085039333 @default.
- W2108678003 cites W2085440534 @default.
- W2108678003 cites W2090134402 @default.
- W2108678003 cites W2093360836 @default.
- W2108678003 cites W2093778666 @default.
- W2108678003 cites W2094758488 @default.
- W2108678003 cites W2102989684 @default.
- W2108678003 cites W2111097284 @default.
- W2108678003 cites W2115734416 @default.
- W2108678003 cites W2129222471 @default.
- W2108678003 cites W2133482423 @default.
- W2108678003 cites W2134759726 @default.
- W2108678003 cites W2135154890 @default.
- W2108678003 cites W2135398566 @default.
- W2108678003 cites W2141781896 @default.
- W2108678003 cites W2143530377 @default.
- W2108678003 cites W2151181348 @default.
- W2108678003 cites W2153354364 @default.
- W2108678003 cites W2162724808 @default.
- W2108678003 cites W2171423579 @default.
- W2108678003 cites W2182889493 @default.
- W2108678003 cites W2343386559 @default.
- W2108678003 cites W3042153938 @default.
- W2108678003 cites W4250007760 @default.
- W2108678003 cites W4294658238 @default.
- W2108678003 doi "https://doi.org/10.1152/ajprenal.00559.2010" @default.
- W2108678003 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3289418" @default.
- W2108678003 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/22114207" @default.
- W2108678003 hasPublicationYear "2012" @default.
- W2108678003 type Work @default.
- W2108678003 sameAs 2108678003 @default.
- W2108678003 citedByCount "45" @default.
- W2108678003 countsByYear W21086780032012 @default.
- W2108678003 countsByYear W21086780032013 @default.
- W2108678003 countsByYear W21086780032014 @default.
- W2108678003 countsByYear W21086780032015 @default.
- W2108678003 countsByYear W21086780032016 @default.
- W2108678003 countsByYear W21086780032017 @default.
- W2108678003 countsByYear W21086780032018 @default.
- W2108678003 countsByYear W21086780032019 @default.
- W2108678003 countsByYear W21086780032020 @default.
- W2108678003 countsByYear W21086780032022 @default.
- W2108678003 countsByYear W21086780032023 @default.
- W2108678003 crossrefType "journal-article" @default.
- W2108678003 hasAuthorship W2108678003A5020999347 @default.
- W2108678003 hasAuthorship W2108678003A5026436514 @default.
- W2108678003 hasAuthorship W2108678003A5035032820 @default.
- W2108678003 hasAuthorship W2108678003A5036727605 @default.
- W2108678003 hasAuthorship W2108678003A5046679319 @default.
- W2108678003 hasAuthorship W2108678003A5058360551 @default.
- W2108678003 hasAuthorship W2108678003A5072402432 @default.
- W2108678003 hasAuthorship W2108678003A5074044567 @default.
- W2108678003 hasAuthorship W2108678003A5076869715 @default.
- W2108678003 hasAuthorship W2108678003A5080064369 @default.
- W2108678003 hasBestOaLocation W21086780032 @default.
- W2108678003 hasConcept C126322002 @default.
- W2108678003 hasConcept C13373296 @default.
- W2108678003 hasConcept C142724271 @default.
- W2108678003 hasConcept C164027704 @default.
- W2108678003 hasConcept C185592680 @default.
- W2108678003 hasConcept C202751555 @default.
- W2108678003 hasConcept C203014093 @default.
- W2108678003 hasConcept C2776252253 @default.