Stimulation of Arginine Transport and Nitric Oxide Production by Lipopolysaccharide Is Mediated by Different Signaling Pathways in Astrocytes

: Transport of l‐arginine and generation of nitrite in microglia‐free astroglial cultures derived from neonatal mouse brain were stimulated by bacterial lipopolysaccharide (LPS) in a time‐ and dose‐dependent manner. LPS stimulated arginine transport between 1.3‐ and 2.5‐fold; half‐maximal stimulatio...

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Veröffentlicht in:Journal of neurochemistry 1995-08, Vol.65 (2), p.590-594
Hauptverfasser: Schmidlin, Andreas, Wiesinger, Heinrich
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description : Transport of l‐arginine and generation of nitrite in microglia‐free astroglial cultures derived from neonatal mouse brain were stimulated by bacterial lipopolysaccharide (LPS) in a time‐ and dose‐dependent manner. LPS stimulated arginine transport between 1.3‐ and 2.5‐fold; half‐maximal stimulation was obtained with 0.3 µg/ml LPS. Acceleration of transport was detectable within 6 h of incubation with LPS. Cycloheximide or actinomycin D neutralized the effect of LPS. Stimulation of generation of nitrite was reduced when the cells were incubated simultaneously with LPS and either genistein or diethyldithiocarbamate, inhibitors of protein tyrosine kinase and nuclear transcription factor κ, respectively. However, stimulation of arginine transport was not reduced in the presence of these compounds. Dexamethasone inhibited stimulation of nitric oxide (NO) production but not of arginine transport. Protein kinase C inhibitor staurosporine had no effect on either process. The results suggest that LPS‐stimulated acceleration of arginine transport in astrocytes requires protein as well as RNA synthesis. Induction of synthesis of an astroglial cationic amino acid transport system appears to be mechanistically independent from stimulation of intracellular NO production.
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LPS stimulated arginine transport between 1.3‐ and 2.5‐fold; half‐maximal stimulation was obtained with 0.3 µg/ml LPS. Acceleration of transport was detectable within 6 h of incubation with LPS. Cycloheximide or actinomycin D neutralized the effect of LPS. Stimulation of generation of nitrite was reduced when the cells were incubated simultaneously with LPS and either genistein or diethyldithiocarbamate, inhibitors of protein tyrosine kinase and nuclear transcription factor κ, respectively. However, stimulation of arginine transport was not reduced in the presence of these compounds. Dexamethasone inhibited stimulation of nitric oxide (NO) production but not of arginine transport. Protein kinase C inhibitor staurosporine had no effect on either process. The results suggest that LPS‐stimulated acceleration of arginine transport in astrocytes requires protein as well as RNA synthesis. 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LPS stimulated arginine transport between 1.3‐ and 2.5‐fold; half‐maximal stimulation was obtained with 0.3 µg/ml LPS. Acceleration of transport was detectable within 6 h of incubation with LPS. Cycloheximide or actinomycin D neutralized the effect of LPS. Stimulation of generation of nitrite was reduced when the cells were incubated simultaneously with LPS and either genistein or diethyldithiocarbamate, inhibitors of protein tyrosine kinase and nuclear transcription factor κ, respectively. However, stimulation of arginine transport was not reduced in the presence of these compounds. Dexamethasone inhibited stimulation of nitric oxide (NO) production but not of arginine transport. Protein kinase C inhibitor staurosporine had no effect on either process. The results suggest that LPS‐stimulated acceleration of arginine transport in astrocytes requires protein as well as RNA synthesis. Induction of synthesis of an astroglial cationic amino acid transport system appears to be mechanistically independent from stimulation of intracellular NO production.</description><subject>Animals</subject><subject>Arginine</subject><subject>Arginine - metabolism</subject><subject>Astrocytes</subject><subject>Astrocytes - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biological Transport - drug effects</subject><subject>Cells, Cultured</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Isolated neuron and nerve. Neuroglia</subject><subject>Lipopolysaccharide</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Mice</subject><subject>Mice, Inbred Strains</subject><subject>Nitric oxide</subject><subject>Nitric Oxide - biosynthesis</subject><subject>Signal Transduction</subject><subject>Transport</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkc1qGzEURkVpSZ20j1AQtHQ3E_2MNBZdGadtEtwkkHQtZEnjyIylqaQhnofIO9cTO96WroT4znfvhQPAZ4xKjCp-vi5xVeOiwkyUWAhWcoYIYgKV2zdgcszegglChBQUVeQ9OE1pjRDmFccn4KTmmBNMJ-D5PrtN36rsgoehgbO4ct55Cx-i8qkLMUPlDbxxOToNb7fOWHgXg-n1S2M5wIXrQhfaISmtH1UcgasEf1njVLZmJC5c09hofYb3buVV6_wK3qn8-KSGBJ2Hs5Rj0EO26QN416g22Y-H9wz8_vH9YX5ZLG5_Xs1ni0JXtEaFbky9FFZQRoTWWjSYEay4NaThhk8JExpZZIxVUybwlClFeKWXNRdaUK0JPQNf93O7GP70NmW5cUnbtlXehj7Juq7QbhH9J4j5lDFBx4nf9qCOIaVoG9lFt1FxkBjJ0Zpcy9GMHM3I0Zp8tSa3u_anw5p-ubHm2D1o2uVfDrlKWrXNzo126YhRJkTFxyMu9tiTa-3wPxfI65v564_-BdA5tx0</recordid><startdate>199508</startdate><enddate>199508</enddate><creator>Schmidlin, Andreas</creator><creator>Wiesinger, Heinrich</creator><general>Blackwell Science Ltd</general><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>199508</creationdate><title>Stimulation of Arginine Transport and Nitric Oxide Production by Lipopolysaccharide Is Mediated by Different Signaling Pathways in Astrocytes</title><author>Schmidlin, Andreas ; Wiesinger, Heinrich</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4370-cfd7b9e93529ccc9f1521a6ed2f6d68259c0e0ddea859185aa264cb769c93cc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Arginine</topic><topic>Arginine - metabolism</topic><topic>Astrocytes</topic><topic>Astrocytes - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biological Transport - drug effects</topic><topic>Cells, Cultured</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Isolated neuron and nerve. Neuroglia</topic><topic>Lipopolysaccharide</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Mice</topic><topic>Mice, Inbred Strains</topic><topic>Nitric oxide</topic><topic>Nitric Oxide - biosynthesis</topic><topic>Signal Transduction</topic><topic>Transport</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schmidlin, Andreas</creatorcontrib><creatorcontrib>Wiesinger, Heinrich</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schmidlin, Andreas</au><au>Wiesinger, Heinrich</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stimulation of Arginine Transport and Nitric Oxide Production by Lipopolysaccharide Is Mediated by Different Signaling Pathways in Astrocytes</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1995-08</date><risdate>1995</risdate><volume>65</volume><issue>2</issue><spage>590</spage><epage>594</epage><pages>590-594</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: Transport of l‐arginine and generation of nitrite in microglia‐free astroglial cultures derived from neonatal mouse brain were stimulated by bacterial lipopolysaccharide (LPS) in a time‐ and dose‐dependent manner. LPS stimulated arginine transport between 1.3‐ and 2.5‐fold; half‐maximal stimulation was obtained with 0.3 µg/ml LPS. Acceleration of transport was detectable within 6 h of incubation with LPS. Cycloheximide or actinomycin D neutralized the effect of LPS. Stimulation of generation of nitrite was reduced when the cells were incubated simultaneously with LPS and either genistein or diethyldithiocarbamate, inhibitors of protein tyrosine kinase and nuclear transcription factor κ, respectively. However, stimulation of arginine transport was not reduced in the presence of these compounds. Dexamethasone inhibited stimulation of nitric oxide (NO) production but not of arginine transport. Protein kinase C inhibitor staurosporine had no effect on either process. The results suggest that LPS‐stimulated acceleration of arginine transport in astrocytes requires protein as well as RNA synthesis. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Animals
Arginine
Arginine - metabolism
Astrocytes
Astrocytes - metabolism
Biological and medical sciences
Biological Transport - drug effects
Cells, Cultured
Fundamental and applied biological sciences. Psychology
Isolated neuron and nerve. Neuroglia
Lipopolysaccharide
Lipopolysaccharides - pharmacology
Mice
Mice, Inbred Strains
Nitric oxide
Nitric Oxide - biosynthesis
Signal Transduction
Transport
Vertebrates: nervous system and sense organs
title Stimulation of Arginine Transport and Nitric Oxide Production by Lipopolysaccharide Is Mediated by Different Signaling Pathways in Astrocytes
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