Document Detail


Effect of endothelin-1 on astrocytic protein content.
MedLine Citation:
PMID:  12730959     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The astrocytic endothelin (ET) receptors, ET(A) and ET(B), modulate calcium signaling and the astrocytic gap junctional network. The nonselective ET receptor ligand ET-1 inhibits gap junction permeability, an effect that can be blocked by tolbutamide. This mechanism may play a role in pathophysiological conditions such as ischemic stroke, characterized by elevated tissue ET-1 levels and hypertrophic-appearing reactive astrocytes. Therefore, the effect of ET-1 on cellular protein content was investigated in confluent once-passaged rat astrocyte cultures under serum-free conditions, by the Lowry method. Gap junction permeability was determined by the dye transfer technique. ET-1 prevented the decrease in astrocytic protein content observed in controls. The effect of ET-1 on cellular protein content was most pronounced in cultures seeded at high density, but it was attenuated in ET(B)-deficient (sl/sl) astrocytes. This effect could be blocked by the nonselective ET antagonist LU 302872 (10 micro M), as well as by the protein synthesis inhibitor cycloheximide (10 micro M). This increase in astrocytic protein content was inhibited by the ATP-sensitive K(+) channel blocker tolbutamide, which also antagonized the ET-1-induced reduction of gap junction permeability and reversed the morphological changes observed in astrocytes upon ET-1 treatment. Cytosine arabinoside (10 micro M), a DNA synthesis blocker, inhibited the ET-1-induced BrdU uptake without affecting the ET-1-induced increase in astrocytic protein content. To conclude, ET-1 induces an increase in astrocytic protein content as well as changes in astrocyte morphology in vitro. This hypertrophic response involves uncoupling of the astrocytic gap junctional network and is not dependent on DNA synthesis.
Authors:
Martin Hasselblatt; Marion Bunte; Ralf Dringen; Arantxa Tabernero; José M Medina; Christian Giaume; Anna-Leena Sirén; Hannelore Ehrenreich
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Glia     Volume:  42     ISSN:  0894-1491     ISO Abbreviation:  Glia     Publication Date:  2003 Jun 
Date Detail:
Created Date:  2003-05-05     Completed Date:  2003-08-04     Revised Date:  2003-11-14    
Medline Journal Info:
Nlm Unique ID:  8806785     Medline TA:  Glia     Country:  United States    
Other Details:
Languages:  eng     Pagination:  390-7     Citation Subset:  IM    
Copyright Information:
Copyright 2003 Wiley-Liss, Inc.
Affiliation:
Max-Planck-Institut für Experimentelle Medizin, Göttingen, Germany.
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MeSH Terms
Descriptor/Qualifier:
Animals
Antimetabolites / pharmacokinetics
Antimetabolites, Antineoplastic / pharmacology
Astrocytes / cytology,  drug effects*,  metabolism*
Bromodeoxyuridine / pharmacokinetics
Cells, Cultured
Cycloheximide / pharmacology
Cytarabine / pharmacology
Endothelin-1 / pharmacology*
Gap Junctions / drug effects,  physiology
Hypoglycemic Agents / pharmacology
Nerve Tissue Proteins / metabolism
Propionic Acids / pharmacology
Protein Synthesis Inhibitors / pharmacology
Pyrimidines / pharmacology
Rats
Rats, Mutant Strains
Rats, Wistar
Receptors, Endothelin / antagonists & inhibitors,  metabolism
Tolbutamide / pharmacology
Chemical
Reg. No./Substance:
0/Antimetabolites; 0/Antimetabolites, Antineoplastic; 0/Endothelin-1; 0/Hypoglycemic Agents; 0/LU 224332; 0/Nerve Tissue Proteins; 0/Propionic Acids; 0/Protein Synthesis Inhibitors; 0/Pyrimidines; 0/Receptors, Endothelin; 147-94-4/Cytarabine; 59-14-3/Bromodeoxyuridine; 64-77-7/Tolbutamide; 66-81-9/Cycloheximide

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