Literature DB >> 1693377

Cellular distribution of transforming growth factor-beta 1 and procollagen types I, III, and IV transcripts in carbon tetrachloride-induced rat liver fibrosis.

H Nakatsukasa1, P Nagy, R P Evarts, C C Hsia, E Marsden, S S Thorgeirsson.   

Abstract

The cellular distribution and temporal expression of transcripts from transforming growth factor-beta 1 (TGF-beta 1) and procollagen alpha 1(I), alpha 1(III), and alpha 1(IV) genes were studied in carbon tetrachloride (CCl4)-induced rat liver fibrosis by using in situ hybridization technique. During the fibrotic process, TGF-beta 1 and procollagen genes were similarly and predominantly expressed in Desmin-positive perisinusoidal cells (e.g., fat-storing cells and myofibroblasts) and fibroblasts and their expression continued to be higher than those observed in control rats. These transcripts were also observed in inflammatory cells mainly granulocytes and macrophage-like cells at the early stages of liver fibrosis. The production of extracellular matrix along small blood vessels and fibrous septa coincided with the expression of these genes. Expression of TGF-beta 1 and procollagen genes were not detected in hepatocytes throughout the experiment. No significant differences in cellular distribution or time course of gene expression among procollagen alpha 1(I), alpha 1(III), and alpha 1(IV) were observed. Desmin-positive perisinusoidal cells and fibroblasts appeared to play the principal role in synthesis of collagens in CCl4-induced hepatic fibrosis. The simultaneous expression of TGF-beta 1 and procollagen genes in mesenchymal cells, including Desmin-positive perisinusoidal cells, during hepatic fibrosis suggests the possibility that TGF-beta 1 may have an important role in the production of fibrosis.

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Year:  1990        PMID: 1693377      PMCID: PMC296648          DOI: 10.1172/JCI114643

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  37 in total

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2.  In situ hybridization for procollagen types I, III and IV mRNA in normal and fibrotic rat liver: evidence for predominant expression in nonparenchymal liver cells.

Authors:  S Milani; H Herbst; D Schuppan; E G Hahn; H Stein
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Review 4.  Collagen formation and cirrhosis.

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Authors:  M G Irving; F J Roll; S Huang; D M Bissell
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7.  Construction of DNA sequences complementary to rat alpha 1 and alpha 2 collagen mRNA and their use in studying the regulation of type I collagen synthesis by 1,25-dihydroxyvitamin D.

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8.  Cell types involved in collagen and fibronectin production in normal and fibrotic human liver.

Authors:  B Clement; J A Grimaud; J P Campion; Y Deugnier; A Guillouzo
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Authors:  F B Bianchi; G Biagini; G Ballardini; G Cenacchi; A Faccani; E Pisi; R Laschi; L Liotta; S Garbisa
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10.  Increased production of collagen in vivo by hepatocytes and nonparenchymal cells in rats with carbon tetrachloride-induced hepatic fibrosis.

Authors:  M Chojkier; K D Lyche; M Filip
Journal:  Hepatology       Date:  1988 Jul-Aug       Impact factor: 17.425

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  80 in total

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7.  CCl4-induced hepatic injury in mice fed a Western diet is associated with blunted healing.

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8.  Hepatic stellate cells and portal fibroblasts are the major cellular sources of collagens and lysyl oxidases in normal liver and early after injury.

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9.  Altered serum transforming growth factor-beta1 and monocyte chemoattractant protein-1 levels in obstructive jaundice.

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10.  Alterations of mast cells and TGF-beta1 on the silymarin treatment for CCl(4)-induced hepatic fibrosis.

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