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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2009-4-27
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pubmed:abstractText |
Cytotoxic T lymphocytes and their granule components, such as perforin and granzyme, play an important role in the defense of hepatic infections caused by different pathogens. Moreover, it has been shown in vitro that hepatocytes can initiate cell death via a perforin-dependent mechanism. Although it is well known that hepatocellular apoptosis in D-galactosamine/lipopolysaccharide (D-Gal/LPS)-associated liver failure is mediated by TNF-alpha-dependent Fas/FasL cytotoxicity, there is no information on the role of perforin-mediated mechanisms in vivo. Therefore, we studied whether the cytolytic perforin/granzyme pathway contributes to the D-Gal/LPS-associated hepatotoxicity. Perforin knockout (Pko) mice showed significantly higher hepatic TNF-alpha and IL-6 mRNA expression as well as plasma TNF-alpha and IL-6 concentrations within the first hour upon D-Gal/LPS challenge compared with perforin wild-type (Pwt) mice. At 6 h upon D-Gal/LPS challenge, Pko mice further presented with higher transaminase release and onconecrotic tissue damage, whereas hepatocellular apoptosis and caspase-3 cleavage remained unaffected by the perforin deficiency. Pretreatment with a recombinant human TNF-alpha receptor fusion protein attenuated necrotic and apoptotic tissue damage and reduced plasma transaminase activities as well as cytokine release, thereby preventing acute liver failure in Pko mice as effectively as in Pwt mice. These data do not only confirm the significance of TNF-alpha as distal mediator of hepatic injury in this model but simultaneously reveal a contribution of a perforin-dependent immunoregulation, limiting the D-Gal/LPS-induced overwhelming cytokine release and onconecrotic tissue injury.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Inflammatory Agents...,
http://linkedlifedata.com/resource/pubmed/chemical/Galactosamine,
http://linkedlifedata.com/resource/pubmed/chemical/Granzymes,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-6,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Pore Forming Cytotoxic Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor,
http://linkedlifedata.com/resource/pubmed/chemical/TNFR-Fc fusion protein,
http://linkedlifedata.com/resource/pubmed/chemical/Transaminases,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/perforin, mouse
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0193-1857
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
296
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
G1069-76
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:19264954-Animals,
pubmed-meshheading:19264954-Anti-Inflammatory Agents, Non-Steroidal,
pubmed-meshheading:19264954-Apoptosis,
pubmed-meshheading:19264954-Disease Models, Animal,
pubmed-meshheading:19264954-Drug-Induced Liver Injury,
pubmed-meshheading:19264954-Galactosamine,
pubmed-meshheading:19264954-Granzymes,
pubmed-meshheading:19264954-Immunoglobulin G,
pubmed-meshheading:19264954-Interleukin-6,
pubmed-meshheading:19264954-Lipopolysaccharides,
pubmed-meshheading:19264954-Liver,
pubmed-meshheading:19264954-Liver Failure, Acute,
pubmed-meshheading:19264954-Male,
pubmed-meshheading:19264954-Mice,
pubmed-meshheading:19264954-Mice, Inbred C57BL,
pubmed-meshheading:19264954-Mice, Knockout,
pubmed-meshheading:19264954-Necrosis,
pubmed-meshheading:19264954-Pore Forming Cytotoxic Proteins,
pubmed-meshheading:19264954-RNA, Messenger,
pubmed-meshheading:19264954-Receptors, Tumor Necrosis Factor,
pubmed-meshheading:19264954-Signal Transduction,
pubmed-meshheading:19264954-T-Lymphocytes, Cytotoxic,
pubmed-meshheading:19264954-Time Factors,
pubmed-meshheading:19264954-Transaminases,
pubmed-meshheading:19264954-Tumor Necrosis Factor-alpha
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pubmed:year |
2009
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pubmed:articleTitle |
Role of the perforin/granzyme cell death pathway in D-Gal/LPS-induced inflammatory liver injury.
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pubmed:affiliation |
Institute for Experimental Surgery, University of Rostock, Rostock, Germany.
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pubmed:publicationType |
Journal Article
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