Neurotensin Stimulates Inositol Phospholipid Metabolism and Calcium Mobilization in Murine Neuroblastoma Clone N1E‐115

Murine neuroblastoma cells (clone N1E‐115) possess neurotensin receptors that mediate cyclic GMP synthesis. Because of the hypothesized relationship between phospholipid metabolism, intracellular Ca2+, and cyclic GMP synthesis, we determined with these cells the effects of neurotensin on 32P labelin...

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Veröffentlicht in:Journal of neurochemistry 1986-10, Vol.47 (4), p.1214-1218
Hauptverfasser: Snider, R. M., Forray, C., Pfenning, M., Richelson, E.
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container_end_page 1218
container_issue 4
container_start_page 1214
container_title Journal of neurochemistry
container_volume 47
creator Snider, R. M.
Forray, C.
Pfenning, M.
Richelson, E.
description Murine neuroblastoma cells (clone N1E‐115) possess neurotensin receptors that mediate cyclic GMP synthesis. Because of the hypothesized relationship between phospholipid metabolism, intracellular Ca2+, and cyclic GMP synthesis, we determined with these cells the effects of neurotensin on 32P labeling of phospholipids, release of inositol phosphates, and intracellular Ca2+ (as determined with the use of Quin‐2, a fluorescent probe sensitive to free Ca2+ levels). Neurotensin stimulated incorporation of 32P into phospholipids, especially phosphatidylinositol and phosphatidate. Neurotensin also stimulated the release of [3H]‐inositol phosphates with an EC50 of about 1 nM. Mean basal Ca2+ concentration in these cells was 134 nM and this level was increased in a rapid and dose‐dependent manner by neurotensin, with an EC50 of 4 nM. Since the EC50 for neurotensin in stimulating cyclic GMP synthesis is 1.5 nM and the KD for binding of [3H]neurotensin at 0° is 11 nM, all these different effects appear to be shared proximal consequences of neurotensin receptor activation.
doi_str_mv 10.1111/j.1471-4159.1986.tb00742.x
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Psychology ; Hormonal regulation ; Inositol - metabolism ; Inositol phosphate ; inositol phosphates ; Inositol Phosphates - metabolism ; Mice ; Molecular and cellular biology ; N1E‐115 ; Neuroblastoma - metabolism ; neuroblastoma cells ; Neurotensin ; Neurotensin - pharmacology ; Phosphatidic Acids - metabolism ; Phosphatidylinositols - metabolism ; Receptors, Neurotensin ; Receptors, Neurotransmitter - physiology</subject><ispartof>Journal of neurochemistry, 1986-10, Vol.47 (4), p.1214-1218</ispartof><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4824-9698c1967bba989e882728ec49d822e98e94193c82b2c6bc1b7f627d9e61fe933</citedby><cites>FETCH-LOGICAL-c4824-9698c1967bba989e882728ec49d822e98e94193c82b2c6bc1b7f627d9e61fe933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-4159.1986.tb00742.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.1986.tb00742.x$$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&amp;idt=7970035$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3018165$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Snider, R. M.</creatorcontrib><creatorcontrib>Forray, C.</creatorcontrib><creatorcontrib>Pfenning, M.</creatorcontrib><creatorcontrib>Richelson, E.</creatorcontrib><title>Neurotensin Stimulates Inositol Phospholipid Metabolism and Calcium Mobilization in Murine Neuroblastoma Clone N1E‐115</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>Murine neuroblastoma cells (clone N1E‐115) possess neurotensin receptors that mediate cyclic GMP synthesis. Because of the hypothesized relationship between phospholipid metabolism, intracellular Ca2+, and cyclic GMP synthesis, we determined with these cells the effects of neurotensin on 32P labeling of phospholipids, release of inositol phosphates, and intracellular Ca2+ (as determined with the use of Quin‐2, a fluorescent probe sensitive to free Ca2+ levels). Neurotensin stimulated incorporation of 32P into phospholipids, especially phosphatidylinositol and phosphatidate. Neurotensin also stimulated the release of [3H]‐inositol phosphates with an EC50 of about 1 nM. Mean basal Ca2+ concentration in these cells was 134 nM and this level was increased in a rapid and dose‐dependent manner by neurotensin, with an EC50 of 4 nM. Since the EC50 for neurotensin in stimulating cyclic GMP synthesis is 1.5 nM and the KD for binding of [3H]neurotensin at 0° is 11 nM, all these different effects appear to be shared proximal consequences of neurotensin receptor activation.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>calcium</subject><subject>Calcium - metabolism</subject><subject>Cell Line</subject><subject>Cell physiology</subject><subject>Clone Cells - metabolism</subject><subject>Cyclic GMP</subject><subject>Cyclic GMP - biosynthesis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hormonal regulation</subject><subject>Inositol - metabolism</subject><subject>Inositol phosphate</subject><subject>inositol phosphates</subject><subject>Inositol Phosphates - metabolism</subject><subject>Mice</subject><subject>Molecular and cellular biology</subject><subject>N1E‐115</subject><subject>Neuroblastoma - metabolism</subject><subject>neuroblastoma cells</subject><subject>Neurotensin</subject><subject>Neurotensin - pharmacology</subject><subject>Phosphatidic Acids - metabolism</subject><subject>Phosphatidylinositols - metabolism</subject><subject>Receptors, Neurotensin</subject><subject>Receptors, Neurotransmitter - physiology</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkcFu1DAQhi1EVbaFR0CyEOKW1ON4Y5sLQlELRd2CBJwt23FUr5x4iROx5cQj9Bn7JCRstFeEL7Y83_wz0ofQKyA5TOdimwPjkDFYyxykKPPBEMIZzfdP0OpYeopWhFCaFYTRZ-gspS0hULISTtFpQUBAuV6h_a0b-zi4LvkOfx18OwY9uISvu5j8EAP-chfT7i4Gv_M13rhBm-mdWqy7Glc6WD-2eBOND_6XHnzs8JSzGXvfOfw32gSdhthqXIU4_8Hl4-8HgPVzdNLokNyL5T5H368uv1Ufs5vPH66r9zeZZYKyTJZSWJAlN0ZLIZ0QlFPhLJO1oNRJ4SQDWVhBDbWlsWB4U1JeS1dC42RRnKM3h9xdH3-MLg2q9cm6EHTn4pgU54RIyeGfIDC2ZhRm8O0BtH1MqXeN2vW-1f29AqJmP2qrZglqlqBmP2rxo_ZT88tlymhaVx9bFyFT_fVS18nq0PS6sz4dMS6ndYsZe3fAfvrg7v9jAfXptgIKrPgDp4muWw</recordid><startdate>198610</startdate><enddate>198610</enddate><creator>Snider, R. 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M. ; Forray, C. ; Pfenning, M. ; Richelson, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4824-9698c1967bba989e882728ec49d822e98e94193c82b2c6bc1b7f627d9e61fe933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>calcium</topic><topic>Calcium - metabolism</topic><topic>Cell Line</topic><topic>Cell physiology</topic><topic>Clone Cells - metabolism</topic><topic>Cyclic GMP</topic><topic>Cyclic GMP - biosynthesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hormonal regulation</topic><topic>Inositol - metabolism</topic><topic>Inositol phosphate</topic><topic>inositol phosphates</topic><topic>Inositol Phosphates - metabolism</topic><topic>Mice</topic><topic>Molecular and cellular biology</topic><topic>N1E‐115</topic><topic>Neuroblastoma - metabolism</topic><topic>neuroblastoma cells</topic><topic>Neurotensin</topic><topic>Neurotensin - pharmacology</topic><topic>Phosphatidic Acids - metabolism</topic><topic>Phosphatidylinositols - metabolism</topic><topic>Receptors, Neurotensin</topic><topic>Receptors, Neurotransmitter - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Snider, R. M.</creatorcontrib><creatorcontrib>Forray, C.</creatorcontrib><creatorcontrib>Pfenning, M.</creatorcontrib><creatorcontrib>Richelson, E.</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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Endocrinology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Snider, R. M.</au><au>Forray, C.</au><au>Pfenning, M.</au><au>Richelson, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neurotensin Stimulates Inositol Phospholipid Metabolism and Calcium Mobilization in Murine Neuroblastoma Clone N1E‐115</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1986-10</date><risdate>1986</risdate><volume>47</volume><issue>4</issue><spage>1214</spage><epage>1218</epage><pages>1214-1218</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>Murine neuroblastoma cells (clone N1E‐115) possess neurotensin receptors that mediate cyclic GMP synthesis. Because of the hypothesized relationship between phospholipid metabolism, intracellular Ca2+, and cyclic GMP synthesis, we determined with these cells the effects of neurotensin on 32P labeling of phospholipids, release of inositol phosphates, and intracellular Ca2+ (as determined with the use of Quin‐2, a fluorescent probe sensitive to free Ca2+ levels). Neurotensin stimulated incorporation of 32P into phospholipids, especially phosphatidylinositol and phosphatidate. Neurotensin also stimulated the release of [3H]‐inositol phosphates with an EC50 of about 1 nM. Mean basal Ca2+ concentration in these cells was 134 nM and this level was increased in a rapid and dose‐dependent manner by neurotensin, with an EC50 of 4 nM. Since the EC50 for neurotensin in stimulating cyclic GMP synthesis is 1.5 nM and the KD for binding of [3H]neurotensin at 0° is 11 nM, all these different effects appear to be shared proximal consequences of neurotensin receptor activation.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>3018165</pmid><doi>10.1111/j.1471-4159.1986.tb00742.x</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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ispartof Journal of neurochemistry, 1986-10, Vol.47 (4), p.1214-1218
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source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects Animals
Biological and medical sciences
calcium
Calcium - metabolism
Cell Line
Cell physiology
Clone Cells - metabolism
Cyclic GMP
Cyclic GMP - biosynthesis
Fundamental and applied biological sciences. Psychology
Hormonal regulation
Inositol - metabolism
Inositol phosphate
inositol phosphates
Inositol Phosphates - metabolism
Mice
Molecular and cellular biology
N1E‐115
Neuroblastoma - metabolism
neuroblastoma cells
Neurotensin
Neurotensin - pharmacology
Phosphatidic Acids - metabolism
Phosphatidylinositols - metabolism
Receptors, Neurotensin
Receptors, Neurotransmitter - physiology
title Neurotensin Stimulates Inositol Phospholipid Metabolism and Calcium Mobilization in Murine Neuroblastoma Clone N1E‐115
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