Source:http://linkedlifedata.com/resource/pubmed/id/15181190
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2004-7-21
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pubmed:abstractText |
IL-8/CXC ligand (CXCL) 8 is ingested in high concentrations by the human fetus/neonate with amniotic fluid and human milk, and is also produced constitutively by intestinal epithelial cells (IEC). We have shown that recombinant human IL-8/CXCL8 (rhIL-8/CXCL8) protects cultured IEC against tumor necrosis factor (TNF)-alpha and cycloheximide-induced cytotoxicity. In view of its constitutive production, we hypothesized that IL-8/CXCL8 might play an autocrine role in fetal enterocyte maintenance. In this study, we measured IL-8/CXCL8 mRNA concentrations in fetal intestine (11-22 wk gestation), sought the presence of the protein by immunohistochemistry in fetal stomach and intestine (9-24 wk), measured IL-8/CXCL8 in neonatal gastric secretions, and studied constitutive and stimulated IL-8/CXCL8 expression in cultured IEC. We found that IL-8/CXCL8 is consistently transcribed and expressed in fetal intestinal tissue, in a developmentally regulated inverse relationship with gestational maturation. The cognate receptors for IL-8/CXCL8 are also expressed abundantly in the fetal intestine, and, therefore, we sought to determine whether the expressed IL-8/CXCL8 would complete an autocrine loop. Neutralization of IL-8/CXCL8 resulted in increased cell death in cultured IEC in the presence of TNF-alpha. This effect is specifically mediated through the CXCR2 receptors. We speculate that IL-8/CXCL8 secretion during cytotoxic stress reflects a cellular self-defense mechanism.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0031-3998
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
240-9
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15181190-Autocrine Communication,
pubmed-meshheading:15181190-Cell Death,
pubmed-meshheading:15181190-Cell Survival,
pubmed-meshheading:15181190-DNA Fragmentation,
pubmed-meshheading:15181190-Female,
pubmed-meshheading:15181190-Fetus,
pubmed-meshheading:15181190-Gestational Age,
pubmed-meshheading:15181190-Humans,
pubmed-meshheading:15181190-Infant,
pubmed-meshheading:15181190-Infant, Newborn,
pubmed-meshheading:15181190-Infant, Premature,
pubmed-meshheading:15181190-Interleukin-8,
pubmed-meshheading:15181190-Intestinal Mucosa,
pubmed-meshheading:15181190-Pregnancy,
pubmed-meshheading:15181190-RNA, Messenger,
pubmed-meshheading:15181190-Receptors, Interleukin-8A,
pubmed-meshheading:15181190-Tumor Necrosis Factor-alpha
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pubmed:year |
2004
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pubmed:articleTitle |
Interleukin-8/CXCL8 forms an autocrine loop in fetal intestinal mucosa.
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pubmed:affiliation |
Division of Neonatology, Department of Pediatrics, University of South Florida College of Medicine, Tampa, FL, USA. Akhil@peds.uab.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, N.I.H., Extramural
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