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 |
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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. |
doi_str_mv | 10.1046/j.1471-4159.1995.65020590.x |
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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><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1046/j.1471-4159.1995.65020590.x</identifier><identifier>PMID: 7616213</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>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</subject><ispartof>Journal of neurochemistry, 1995-08, Vol.65 (2), p.590-594</ispartof><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4370-cfd7b9e93529ccc9f1521a6ed2f6d68259c0e0ddea859185aa264cb769c93cc23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1471-4159.1995.65020590.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1471-4159.1995.65020590.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3599462$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7616213$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schmidlin, Andreas</creatorcontrib><creatorcontrib>Wiesinger, Heinrich</creatorcontrib><title>Stimulation of Arginine Transport and Nitric Oxide Production by Lipopolysaccharide Is Mediated by Different Signaling Pathways in Astrocytes</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><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.</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. Induction of synthesis of an astroglial cationic amino acid transport system appears to be mechanistically independent from stimulation of intracellular NO production.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>7616213</pmid><doi>10.1046/j.1471-4159.1995.65020590.x</doi><tpages>5</tpages></addata></record> |
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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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