Literature DB >> 11753205

The hepatocyte as a microbial product-responsive cell.

Y Vodovotz1, S Liu, C McCloskey, R Shapiro, A Green, T R Billiar.   

Abstract

Much research has focused on the responses to microbial products of immune cells such as monocytes, macrophages, and neutrophils. Although the liver is a primary response organ in various infections, relatively little is known about the antimicrobial responses of its major cell type, the hepatocyte. It is now known that the recognition of bacteria occurs via cell-surface proteins that are members of the Toll-like receptor (TLR) family. In addition, lipopolysaccharide (LPS) is bound by circulating LPS-binding protein (LBP) and presented to cell-surface CD14, which in turn interacts with TLR and transduces an intracellular signal. We investigated the CD14 and TLR2 responses of whole liver and isolated hepatocytes, and demonstrated that these cells can be induced to express the molecules necessary for responses to both Gram-positive and Gram-negative bacteria. Our findings may have clinical implications for pathological states such as sepsis.

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Year:  2001        PMID: 11753205

Source DB:  PubMed          Journal:  J Endotoxin Res        ISSN: 0968-0519


  21 in total

Review 1.  Hepatocytes as Immunological Agents.

Authors:  Ian N Crispe
Journal:  J Immunol       Date:  2016-01-01       Impact factor: 5.422

Review 2.  The role of innate immunity in HBV infection.

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Journal:  Semin Immunopathol       Date:  2012-07-20       Impact factor: 9.623

3.  Stressed erythrophagocytosis induces immunosuppression during sepsis through heme-mediated STAT1 dysregulation.

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Journal:  J Clin Invest       Date:  2021-01-04       Impact factor: 14.808

4.  Hepatocytes express functional NOD1 and NOD2 receptors: a role for NOD1 in hepatocyte CC and CXC chemokine production.

Authors:  Melanie J Scott; Christine Chen; Qian Sun; Timothy R Billiar
Journal:  J Hepatol       Date:  2010-06-16       Impact factor: 25.083

5.  Lipopolysaccharide opposes the induction of CYP26A1 and CYP26B1 gene expression by retinoic acid in the rat liver in vivo.

Authors:  Reza Zolfaghari; Christopher J Cifelli; Siam O Lieu; Qiuyan Chen; Nan-qian Li; A Catharine Ross
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2006-12-21       Impact factor: 4.052

6.  TRAF6-NF-kappaB pathway is essential for interleukin-1-induced TLR2 expression and its functional response to TLR2 ligand in murine hepatocytes.

Authors:  Takayuki Matsumura; Takahiro Degawa; Takemasa Takii; Hidetoshi Hayashi; Takashi Okamoto; Jun-ichiro Inoue; Kikuo Onozaki
Journal:  Immunology       Date:  2003-05       Impact factor: 7.397

7.  Up-regulated TLR2 and TLR4 expressions in liver and spleen during acute murine T. gondii infection.

Authors:  Jialing Peng; Xiancan Lin; Hongchun Lin; Shengjie Chen; Jinfeng Liu; Zexin Guo; Yuqing Liang; Shiguang Huang; Fangli Lu
Journal:  Parasitol Res       Date:  2016-08-17       Impact factor: 2.289

8.  Endotoxin uptake in mouse liver is blocked by endotoxin pretreatment through a suppressor of cytokine signaling-1-dependent mechanism.

Authors:  Melanie J Scott; Shubing Liu; Richard A Shapiro; Yoram Vodovotz; Timothy R Billiar
Journal:  Hepatology       Date:  2009-05       Impact factor: 17.425

9.  Beta2-integrin-induced p38 MAPK activation is a key mediator in the CD14/TLR4/MD2-dependent uptake of lipopolysaccharide by hepatocytes.

Authors:  Melanie J Scott; Timothy R Billiar
Journal:  J Biol Chem       Date:  2008-08-13       Impact factor: 5.157

10.  Human SR-BI and SR-BII Potentiate Lipopolysaccharide-Induced Inflammation and Acute Liver and Kidney Injury in Mice.

Authors:  Irina N Baranova; Ana C P Souza; Alexander V Bocharov; Tatyana G Vishnyakova; Xuzhen Hu; Boris L Vaisman; Marcelo J Amar; Zhigang Chen; Yana Kost; Alan T Remaley; Amy P Patterson; Peter S T Yuen; Robert A Star; Thomas L Eggerman
Journal:  J Immunol       Date:  2016-03-02       Impact factor: 5.422

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