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PMID: 9178851 Published · ppublish English Journal Article

The angiotensin AT2 receptor down-regulates neurofilament M in PC12W cells.

Neuroscience letters ·Vol. 227 ·No. 1 ·1997-05-09 ·Pages 29-32

Gallinat S, Csikos T, Meffert S, Herdegen T, Stoll M, Unger T

Abstract

The angiotensin (ANG II) AT2 receptor mediates antiproliferative effects and induces neurite outgrowth in PC12W cells. To further investigate the molecular events following AT2 receptor stimulation in these cells, we determined the expression pattern of the middle-sized neurofilament subunit (NF-M) using Western and Northern blot analysis and reverse-transcription polymerase chain reaction. On both, the protein and the mRNA level, ANG II via AT2 receptors not only counteracted nerve growth factor (NGF)-mediated NF-M up-regulation but also reduced NF-M levels in the absence of NGF by maximally 72%. The ANG II-induced effects were completely abolished by pretreatment with the AT2 receptor antagonist, PD123177. In view of previous findings of decreased NF levels in regenerating neurons and in neuronal cultures undergoing apoptosis, our observation suggests a new role of AT2 receptors in either of these processes.

MeSH Terms
Angiotensin Receptor Antagonists Animals Biphenyl Compounds/pharmacology Cell Differentiation/physiology Down-Regulation Imidazoles/pharmacology Linear Models Losartan Neurofilament Proteins/metabolism PC12 Cells Polymerase Chain Reaction/methods Rats Receptors, Angiotensin/physiology Tetrazoles/pharmacology Transcription, Genetic
Chemicals
Angiotensin Receptor Antagonists Biphenyl Compounds Imidazoles Neurofilament Proteins Receptors, Angiotensin Tetrazoles Losartan
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Gallinat S
Department of Pharmacology, Christian-Albrechts-University, Kiel, Germany.
Csikos T
Meffert S
Herdegen T
Stoll M
Unger T
Article Info
Journal
Neuroscience letters
Abbr.
Neurosci Lett
ISSN
0304-3940
Published
1997-05-09
Pages
29-32
Language
English
Region
Ireland
NLM ID
7600130
Subset
IM
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