Publikationsserver der RWTH Aachen University
Untersuchungen zur Rolle von Zytokinen bei der Beta-2-Mikroglobulin-Synthese in verschiedenen humanen Zelltypen
Abstract
dc:descriptionBackground. Proinflammatory monocytic cytokines such as interleukin-1 (IL-1), tumour necrosis factor-alpha (TNF-alpha) and IL-6 have been incriminated in the pathogenesis of elevated beta-2-microglobulin (beta-2-M) serum concentrations in patients undergoing haemodialysis with so-called bioincompatible dialyser membranes. However, neither the source of the elevated serum beta-2-M nor the precise role of monocytic cytokines in the expression of the beta-2-M gene have been elucidated conclusively. The aim of this study was to evaluate whether monoytic cytokines, and in particular IL-6, are regulators of beta-2-M gene expression in human hepatoma cells, T-lymphocytes and monocytes. Methods. HepG2 and HuH7 human hepatoma cells, Jurkat T-cells, monocytic MonoMac6 cells, primary human monocytes and synoviocytes were stimulated with IL-1-beta, IL-6, interferon-alpha (IFN-alpha), IFN-gamma or conditioned media from lipopolysaccharide (LPS)-treated monocytes. Expression of beta-2-M mRNA was analysed by Northern blotting, beta-2-M protein synthesis was determined by metabolic labelling and immunoprecipitation, and beta-2-M secretion was measured by an enzyme-linked immunosorbent assay (ELISA). Results. In all cell types tested, IFN-gamma and, to a lesser extent, IFN-alpha stimulated gene expression of beta-2-M resulting in an increased synthesis and secretion of beta-2-M protein. Neither IL-1-beta and IL-6 nor supernatants from LPS-treated monocytes were capable of inducing beta-2-M gene expression, with the exception of a small increase in HuH7 hepatoma cells upon IL-1-beta treatment. Conclusions. The present study provides evidence that interferons are important regulators of beta-2-M expression. It also shows that proinflammatory monocytic cytokines do not modulate directly the expression of beta-2-M in cells of hepatic, monocytic and T-lymphocytic origin. Whether they are other inflammatory influences to the bioincompability of dialyser membranes is discussed in this study.
Degree
thesis:*- Grantor dc:publisher
- Publikationsserver der RWTH Aachen University
- Year dc:date
- 2006
Author and committee
dc:creator, dc:contributor.*- Author dc:creator
-
- Vraetz, Thomas
- Contributors dc:contributor
-
- Graeve, Lutz
Subjects
dc:subject × 19- info:eu-repo/classification/ddc/610
- Amyloidose
- Mikroglobulin <beta-2->
- Dialyse
- Interleukin 6
- Interleukin 1
- Interferon <gamma->
- Interferon
- Interferon <alpha->
- Medizin
- Bioinkompatibilität
- Zytokine
- Hämodialyse
- Beta-2-Mikroglobulin
- bioincompatibility
- cytokines
- haemodialysis
- beta-2-microglobulin
- amyloidosis
Rights
dc:rights- Statement dc:rights
-
- info:eu-repo/semantics/openAccess
- Language dc:language
- ger
Identifiers
dc:identifier.*- OAI identifier oai:identifier
- oai:publications.rwth-aachen.de:61519