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Endotoxin and cytokines increase hepatic messenger RNA levels and serum concentrations of apolipoprotein J (clusterin) in Syrian hamsters

Endotoxin and cytokines increase hepatic messenger RNA levels and serum concentrations of apolipoprotein J (clusterin) in Syrian hamsters


Title: Endotoxin and cytokines increase hepatic messenger RNA levels and serum concentrations of apolipoprotein J (clusterin) in Syrian hamsters
Author: Harðardóttir, Ingibjörg
Kunitake, Steven T.
Moser, A. H.
Doerrler, William
Rapp, Joseph H.
Grunfeld, Carl
Feingold, Kenneth R.
Date: 1994-09
Language: English
Scope: 6
University/Institute: Landspitali - The National University Hospital of Iceland
Department: Clinical Laboratory Services, Diagnostics and Blood Bank
Faculty of Medicine
Series: Journal of Clinical Investigation; 94(3)
ISSN: 0021-9738
DOI: 10.1172/JCI117449
Subject: acute phase reaction; HDL; immunologic factors; lipopolysaccharides; lipoproteins; General Medicine
URI: https://hdl.handle.net/20.500.11815/3630

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Citation:

Harðardóttir , I , Kunitake , S T , Moser , A H , Doerrler , W , Rapp , J H , Grunfeld , C & Feingold , K R 1994 , ' Endotoxin and cytokines increase hepatic messenger RNA levels and serum concentrations of apolipoprotein J (clusterin) in Syrian hamsters ' , Journal of Clinical Investigation , vol. 94 , no. 3 , pp. 1304-1309 . https://doi.org/10.1172/JCI117449

Abstract:

Infection and inflammation induce alterations in hepatic synthesis and plasma concentrations of the acute phase proteins. Our results show that apolipoprotein (apo) J is a positive acute phase protein. Endotoxin (LPS), tumor necrosis factor (TNF), and interleukin (IL)-1 increased hepatic mRNA and serum protein levels of apo J in Syrian hamsters. Hepatic apo J mRNA levels increased 10- to 15-fold with doses of LPS from 0.1 to 100 μg/100 g body weight within 4 h and were elevated for ≥ 24 h. Serum apo J concentrations were significantly increased by 16 h and further elevated to 3.3 times that of control, 24 h after LPS administration. Serum apo J was associated with high density lipoprotein and increased fivefold in this fraction, after LPS administration. Hepatic apo J mRNA levels increased 3.5- and 4.6-fold, with TNF and IL-1, respectively, and 8.2-fold with a combination of TNF and IL-1. Serum apo J concentrations were increased 2.3- fold by TNF, 79% by IL-1, and 2.9-fold with a combination of TNF and IL-1. These results demonstrate that apo J is a positive acute phase protein.

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