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PMID: 2108188 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Transforming growth factors type beta 1 and beta 2 suppress rat astrocyte autoantigen presentation and antagonize hyperinduction of class II major histocompatibility complex antigen expression by interferon-gamma and tumor necrosis factor-alpha.

Journal of neuroimmunology ·Vol. 27 ·No. 1 ·1990-04-00 ·Pages 41-7

Schluesener HJ

Abstract

The transforming growth factors (TGF) type beta 1 and beta 2 are regulatory cytokines strongly affecting rat astrocyte immune functions. Both cytokines suppressed presentation of autoantigen by astrocytes: highly encephalitogenic T cells cocultured with TGF-beta-treated astrocytes in the presence of myelin basic protein did not become activated to transfer experimental allergic encephalomyelitis, a central nervous system (CNS) autoimmune disease. Furthermore, TGF-beta 1 and -beta 2 antagonized hyperinduction of astrocyte major histocompatibility complex (MHC) class II antigen expression by interferon-gamma and tumor necrosis factor-alpha. Thus, TGF-beta might be a potential regulator of CNS inflammation.

MeSH Terms
Animals Antigen-Presenting Cells/drug effects Astrocytes/immunology,metabolism Autoantigens/immunology Cell Line Dinoprostone/metabolism Histocompatibility Antigens Class II/immunology Indomethacin/pharmacology Interferon-gamma/pharmacology Rats Transforming Growth Factors/physiology Tumor Necrosis Factor-alpha/pharmacology
Chemicals
Autoantigens Histocompatibility Antigens Class II Tumor Necrosis Factor-alpha Transforming Growth Factors Interferon-gamma Dinoprostone Indomethacin
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Schluesener H J
Clinical Research Unit for Multiple Sclerosis, Max-Planck-Society, Würzburg, F.R.G.
Article Info
Journal
Journal of neuroimmunology
Abbr.
J Neuroimmunol
ISSN
0165-5728
Published
1990-04-00
Pages
41-7
Language
English
Region
Netherlands
NLM ID
8109498
Subset
IM
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