Cytokine expression in three mouse models of experimental hepatitis.

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Cytokine expression in three mouse models of experimental hepatitis. / Sass, Gabriele; Heinlein, Sonja; Agli, Andrea; Bang, Renate; Schümann, Jens; Tiegs, Gisa.

In: CYTOKINE, Vol. 19, No. 3, 3, 2002, p. 115-120.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Sass, G, Heinlein, S, Agli, A, Bang, R, Schümann, J & Tiegs, G 2002, 'Cytokine expression in three mouse models of experimental hepatitis.', CYTOKINE, vol. 19, no. 3, 3, pp. 115-120. <http://www.ncbi.nlm.nih.gov/pubmed/12242077?dopt=Citation>

APA

Vancouver

Sass G, Heinlein S, Agli A, Bang R, Schümann J, Tiegs G. Cytokine expression in three mouse models of experimental hepatitis. CYTOKINE. 2002;19(3):115-120. 3.

Bibtex

@article{802bab14ee12456bb8f5442a697ddaa7,
title = "Cytokine expression in three mouse models of experimental hepatitis.",
abstract = "The activation of T-cells and macrophages and subsequent induction of cytokines are critical factors in the development of hepatitis. Up-regulation of pro-inflammatory cytokines, e.g. TNF has been shown to induce liver injury while counter regulation by anti-inflammatory cytokines, e.g. IL-10 is protective. We compared the induction of liver injury and the expression pattern of a variety of cytokines in T-cell- versus non-T-cell-dependent mouse models of liver injury. TNF, IFNgamma, IL-2, IL-4, IL-6, IL-10 and IL-12 were measured in plasma and liver tissue after either Concanavalin A (Con A), D-galactosamine/lipopolysaccharide (GalN/LPS) or high dose LPS induced liver injury. Additionally, the intra-hepatic expression of the putative pathogenicity factor high mobility group 1 protein (HMG-1) was compared in all three models.",
keywords = "Animals, Time Factors, Disease Models, Animal, Mice, Mice, Inbred BALB C, Up-Regulation, Kinetics, Reverse Transcriptase Polymerase Chain Reaction, Molecular Sequence Data, Enzyme-Linked Immunosorbent Assay, Interferon-gamma/biosynthesis, Galactosamine/pharmacology, Concanavalin A/pharmacology, Interleukin-6/biosynthesis, Tumor Necrosis Factor-alpha/biosynthesis, Interleukin-10/biosynthesis, Cytokines/*biosynthesis/*blood, Hepatitis/*blood, Interleukin-12/biosynthesis, Interleukin-2/biosynthesis, Interleukin-4/biosynthesis, Lipopolysaccharides/pharmacology, Liver/injuries, Animals, Time Factors, Disease Models, Animal, Mice, Mice, Inbred BALB C, Up-Regulation, Kinetics, Reverse Transcriptase Polymerase Chain Reaction, Molecular Sequence Data, Enzyme-Linked Immunosorbent Assay, Interferon-gamma/biosynthesis, Galactosamine/pharmacology, Concanavalin A/pharmacology, Interleukin-6/biosynthesis, Tumor Necrosis Factor-alpha/biosynthesis, Interleukin-10/biosynthesis, Cytokines/*biosynthesis/*blood, Hepatitis/*blood, Interleukin-12/biosynthesis, Interleukin-2/biosynthesis, Interleukin-4/biosynthesis, Lipopolysaccharides/pharmacology, Liver/injuries",
author = "Gabriele Sass and Sonja Heinlein and Andrea Agli and Renate Bang and Jens Sch{\"u}mann and Gisa Tiegs",
year = "2002",
language = "English",
volume = "19",
pages = "115--120",
journal = "CYTOKINE",
issn = "1043-4666",
publisher = "Academic Press Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Cytokine expression in three mouse models of experimental hepatitis.

AU - Sass, Gabriele

AU - Heinlein, Sonja

AU - Agli, Andrea

AU - Bang, Renate

AU - Schümann, Jens

AU - Tiegs, Gisa

PY - 2002

Y1 - 2002

N2 - The activation of T-cells and macrophages and subsequent induction of cytokines are critical factors in the development of hepatitis. Up-regulation of pro-inflammatory cytokines, e.g. TNF has been shown to induce liver injury while counter regulation by anti-inflammatory cytokines, e.g. IL-10 is protective. We compared the induction of liver injury and the expression pattern of a variety of cytokines in T-cell- versus non-T-cell-dependent mouse models of liver injury. TNF, IFNgamma, IL-2, IL-4, IL-6, IL-10 and IL-12 were measured in plasma and liver tissue after either Concanavalin A (Con A), D-galactosamine/lipopolysaccharide (GalN/LPS) or high dose LPS induced liver injury. Additionally, the intra-hepatic expression of the putative pathogenicity factor high mobility group 1 protein (HMG-1) was compared in all three models.

AB - The activation of T-cells and macrophages and subsequent induction of cytokines are critical factors in the development of hepatitis. Up-regulation of pro-inflammatory cytokines, e.g. TNF has been shown to induce liver injury while counter regulation by anti-inflammatory cytokines, e.g. IL-10 is protective. We compared the induction of liver injury and the expression pattern of a variety of cytokines in T-cell- versus non-T-cell-dependent mouse models of liver injury. TNF, IFNgamma, IL-2, IL-4, IL-6, IL-10 and IL-12 were measured in plasma and liver tissue after either Concanavalin A (Con A), D-galactosamine/lipopolysaccharide (GalN/LPS) or high dose LPS induced liver injury. Additionally, the intra-hepatic expression of the putative pathogenicity factor high mobility group 1 protein (HMG-1) was compared in all three models.

KW - Animals

KW - Time Factors

KW - Disease Models, Animal

KW - Mice

KW - Mice, Inbred BALB C

KW - Up-Regulation

KW - Kinetics

KW - Reverse Transcriptase Polymerase Chain Reaction

KW - Molecular Sequence Data

KW - Enzyme-Linked Immunosorbent Assay

KW - Interferon-gamma/biosynthesis

KW - Galactosamine/pharmacology

KW - Concanavalin A/pharmacology

KW - Interleukin-6/biosynthesis

KW - Tumor Necrosis Factor-alpha/biosynthesis

KW - Interleukin-10/biosynthesis

KW - Cytokines/biosynthesis/blood

KW - Hepatitis/blood

KW - Interleukin-12/biosynthesis

KW - Interleukin-2/biosynthesis

KW - Interleukin-4/biosynthesis

KW - Lipopolysaccharides/pharmacology

KW - Liver/injuries

KW - Animals

KW - Time Factors

KW - Disease Models, Animal

KW - Mice

KW - Mice, Inbred BALB C

KW - Up-Regulation

KW - Kinetics

KW - Reverse Transcriptase Polymerase Chain Reaction

KW - Molecular Sequence Data

KW - Enzyme-Linked Immunosorbent Assay

KW - Interferon-gamma/biosynthesis

KW - Galactosamine/pharmacology

KW - Concanavalin A/pharmacology

KW - Interleukin-6/biosynthesis

KW - Tumor Necrosis Factor-alpha/biosynthesis

KW - Interleukin-10/biosynthesis

KW - Cytokines/biosynthesis/blood

KW - Hepatitis/blood

KW - Interleukin-12/biosynthesis

KW - Interleukin-2/biosynthesis

KW - Interleukin-4/biosynthesis

KW - Lipopolysaccharides/pharmacology

KW - Liver/injuries

M3 - SCORING: Journal article

VL - 19

SP - 115

EP - 120

JO - CYTOKINE

JF - CYTOKINE

SN - 1043-4666

IS - 3

M1 - 3

ER -