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PMID: 3017995 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Monocyte-conditioned medium, interleukin-1, and tumor necrosis factor stimulate the acute phase response in human hepatoma cells in vitro.

The Journal of cell biology ·Vol. 103 ·No. 3 ·1986-09-00 ·Pages 787-93

Darlington GJ, Wilson DR, Lachman LB

Abstract

Human hepatoma cells mimic the acute phase response after treatment with monocyte-conditioned medium. Levels of secreted fibrinogen, alpha-1 acid glycoprotein, C-reactive protein, haptoglobin, and the third component of complement were elevated compared with control levels after 48 h of incubation with conditioned supernatant medium from an enriched fraction of normal peripheral monocytes. Albumin levels declined and alpha-1 antitrypsin remained unchanged. Levels of specific mRNA were measured by hybridization to slot blots and Northern blots and changed in correspondence with protein alterations. Interleukin-1 and tumor necrosis factor stimulated the third component of complement, but did not elevate any other member of the acute phase group and were therefore only partially active in this system. The identification of an in vitro model of the human acute phase response will permit analysis of the molecular basis for coordinate regulation of this group of facultative genes.

MeSH Terms
C-Reactive Protein/biosynthesis Carcinoma, Hepatocellular Cell Line DNA Glycoproteins/pharmacology Humans Inflammation Interleukin-1/pharmacology Liver/drug effects Liver Neoplasms Lymphokines/pharmacology RNA, Messenger/analysis Tumor Necrosis Factor-alpha
Chemicals
Glycoproteins Interleukin-1 Lymphokines RNA, Messenger Tumor Necrosis Factor-alpha C-Reactive Protein DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Darlington G J
Wilson D R
Lachman L B
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35 references, click to expand
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1986-09-00
Pages
787-93
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2114283
Subset
IM
Grants
NIGMS NIH HHS · GM-32111 · United States
Analysis Services
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