Literature DB >> 17264982

Rat chemokine CXCL11: structure, tissue distribution, function and expression in cardiac transplantation models.

Noboru Mitsuhashi1, Gordon D Wu, Hui Zhu, Mary Kearns-Jonker, Donald V Cramer, Vaughn A Starnes, Mark L Barr.   

Abstract

CXCL11 is thought to play a critical role in allograft rejection. To clarify the role of CXCL11 in the rat transplantation model, we cloned CXCL11 cDNA from rat liver tissue and used it to study CXCL11 structure, function and expression. The rat CXCL11 gene encodes a protein of 100 amino acids and spans approximately a 2.8 kb DNA segment containing 4 exons in the protein coding region. Tissue distribution of rat CXCL11 was analyzed by quantitative RT-PCR and showed that rat CXCL11 mRNA is expressed in various tissues and, in particular, at high levels in the spleen and lymph nodes. COS-1 cells were transfected with a plasmid vector encoding rat CXCL11 and used to study CXCL11 effects on cell migration and internalization of CXCR3, the CXCL11 receptor. The recombinant CXCL11 showed chemotactic properties and induced CXCR3 internalization in CD4(+) T cells. Expression of CXCL11 mRNA also was measured in rat acute (ACI to LEW) and chronic (LEW to F344) heart transplant rejection models. CXCL11 mRNA expression in allografts increased in both models, compared with controls, and was primarily observed in infiltrating macrophages and donor endothelial cells. These results indicate that, like the other CXCR3 chemokines, rat CXCL11 seems to have a role in the homing of CD4(+) T cells in both acute and chronic rejection models of heart allotransplantation.

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Year:  2007        PMID: 17264982     DOI: 10.1007/s11010-005-9010-9

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  49 in total

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Review 4.  Immunopathology of cardiac transplant rejection.

Authors:  R J Duquesnoy; A J Demetris
Journal:  Curr Opin Cardiol       Date:  1995-03       Impact factor: 2.161

5.  Structure and expression of the human small cytokine B subfamily member 11 (SCYB11/formerly SCYB9B, alias I-TAC) gene cloned from IFN-gamma-treated human monocytes (THP-1).

Authors:  A Laich; M Meyer; E R Werner; G Werner-Felmayer
Journal:  J Interferon Cytokine Res       Date:  1999-05       Impact factor: 2.607

6.  Switch in chemokine receptor expression upon TCR stimulation reveals novel homing potential for recently activated T cells.

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Journal:  Eur J Immunol       Date:  1999-06       Impact factor: 5.532

7.  Differential expression of the chemokine receptors by the Th1- and Th2-type effector populations within circulating CD4+ T cells.

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8.  Molecular characterization of the chemokine receptor CXCR3: evidence for the involvement of distinct extracellular domains in a multi-step model of ligand binding and receptor activation.

Authors:  Georgina Xanthou; Timothy J Williams; James E Pease
Journal:  Eur J Immunol       Date:  2003-10       Impact factor: 5.532

9.  Genome sequence of the Brown Norway rat yields insights into mammalian evolution.

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Journal:  Nature       Date:  2004-04-01       Impact factor: 49.962

10.  Chemokine and chemokine receptor gene expression indicates acute rejection of human cardiac transplants.

Authors:  Nader M Fahmy; Mohamad H Yamani; Randall C Starling; Norman B Ratliff; James B Young; Patrick M McCarthy; Jingyuan Feng; Andrew C Novick; Robert L Fairchild
Journal:  Transplantation       Date:  2003-01-15       Impact factor: 4.939

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  5 in total

Review 1.  Immune Cell Trafficking to the Liver.

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Journal:  Transplantation       Date:  2019-07       Impact factor: 4.939

2.  Organization and promoter analysis of the zebrafish (Danio rerio) chemokine gene (CXC-64) promoter.

Authors:  Li-Chen Chen; Jen-Leih Wu; Chyuan-Yuan Shiau; Jyh-Yih Chen
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3.  Toxicity of nickel ions and comprehensive analysis of nickel ion-associated gene expression profiles in THP-1 cells.

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Review 4.  Chemokines in chronic liver allograft dysfunction pathogenesis and potential therapeutic targets.

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Review 5.  Typical and atypical properties of peripheral nerve allografts enable novel strategies to repair segmental-loss injuries.

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