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 |
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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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M. ; Forray, C. ; Pfenning, M. ; Richelson, E.</creator><creatorcontrib>Snider, R. M. ; Forray, C. ; Pfenning, M. ; Richelson, E.</creatorcontrib><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><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.1986.tb00742.x</identifier><identifier>PMID: 3018165</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>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</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&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. M.</creator><creator>Forray, C.</creator><creator>Pfenning, M.</creator><creator>Richelson, E.</creator><general>Blackwell Publishing 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>7QP</scope><scope>7SQ</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>198610</creationdate><title>Neurotensin Stimulates Inositol Phospholipid Metabolism and Calcium Mobilization in Murine Neuroblastoma Clone N1E‐115</title><author>Snider, R. 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 & 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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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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