The Physiologic Concentration of Inositol 1,4,5-Trisphosphate in the Oocytes of Xenopus laevis
To measure the concentration of inositol 1,4,5-trisphosphate ([IP3]) in small regions of single Xenopus oocytes, a biological detector cell was combined with capillary electrophoresis. This method is 10,000 times more sensitive than all existing assays enabling subcellular measurement of [IP3] in Xe...
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Veröffentlicht in: | The Journal of biological chemistry 1998-10, Vol.273 (44), p.28657-28662 |
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creator | Luzzi, Veronica Sims, Christopher E. Soughayer, Joseph S. Allbritton, Nancy L. |
description | To measure the concentration of inositol 1,4,5-trisphosphate ([IP3]) in small regions of single Xenopus oocytes, a biological detector cell was combined with capillary electrophoresis. This method is 10,000 times more sensitive than all existing assays enabling subcellular measurement of [IP3] in Xenopus oocytes. Upon addition of lysophosphatidic acid to an oocyte, [IP3] increased from 40 to 650 nm within 2 min. IP3concentrations as high as 1.8 μm were measured after activation with lysophosphatidic acid, suggesting that the physiologic concentration of IP3 ranges from the tens of nanomolar to a few micromolar in Xenopus oocytes. Since the IP3 receptor in Xenopus oocytes is nearly identical to the type I receptor of mammalian cells, the range of [IP3] in most mammalian cells is likely to be similar to that in the oocyte. By selecting or engineering the appropriate detector cell, this strategy should be applicable to cyclic adenosine diphosphate ribose and nicotinic acid adenine dinucleotide phosphate, and to the discovery of new Ca2+-releasing second messengers. |
doi_str_mv | 10.1074/jbc.273.44.28657 |
format | Article |
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This method is 10,000 times more sensitive than all existing assays enabling subcellular measurement of [IP3] in Xenopus oocytes. Upon addition of lysophosphatidic acid to an oocyte, [IP3] increased from 40 to 650 nm within 2 min. IP3concentrations as high as 1.8 μm were measured after activation with lysophosphatidic acid, suggesting that the physiologic concentration of IP3 ranges from the tens of nanomolar to a few micromolar in Xenopus oocytes. Since the IP3 receptor in Xenopus oocytes is nearly identical to the type I receptor of mammalian cells, the range of [IP3] in most mammalian cells is likely to be similar to that in the oocyte. By selecting or engineering the appropriate detector cell, this strategy should be applicable to cyclic adenosine diphosphate ribose and nicotinic acid adenine dinucleotide phosphate, and to the discovery of new Ca2+-releasing second messengers.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.273.44.28657</identifier><identifier>PMID: 9786859</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Calcium Signaling ; Cell Line ; Electrophoresis, Capillary ; Freshwater ; Guinea Pigs ; Inositol 1,4,5-Trisphosphate - metabolism ; Inositol 1,4,5-Trisphosphate - physiology ; Oocytes - metabolism ; Oocytes - physiology ; PC12 Cells ; Rats ; Spectrometry, Fluorescence ; Xenopus laevis</subject><ispartof>The Journal of biological chemistry, 1998-10, Vol.273 (44), p.28657-28662</ispartof><rights>1998 © 1998 ASBMB. 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This method is 10,000 times more sensitive than all existing assays enabling subcellular measurement of [IP3] in Xenopus oocytes. Upon addition of lysophosphatidic acid to an oocyte, [IP3] increased from 40 to 650 nm within 2 min. IP3concentrations as high as 1.8 μm were measured after activation with lysophosphatidic acid, suggesting that the physiologic concentration of IP3 ranges from the tens of nanomolar to a few micromolar in Xenopus oocytes. Since the IP3 receptor in Xenopus oocytes is nearly identical to the type I receptor of mammalian cells, the range of [IP3] in most mammalian cells is likely to be similar to that in the oocyte. By selecting or engineering the appropriate detector cell, this strategy should be applicable to cyclic adenosine diphosphate ribose and nicotinic acid adenine dinucleotide phosphate, and to the discovery of new Ca2+-releasing second messengers.</description><subject>Animals</subject><subject>Calcium Signaling</subject><subject>Cell Line</subject><subject>Electrophoresis, Capillary</subject><subject>Freshwater</subject><subject>Guinea Pigs</subject><subject>Inositol 1,4,5-Trisphosphate - metabolism</subject><subject>Inositol 1,4,5-Trisphosphate - physiology</subject><subject>Oocytes - metabolism</subject><subject>Oocytes - physiology</subject><subject>PC12 Cells</subject><subject>Rats</subject><subject>Spectrometry, Fluorescence</subject><subject>Xenopus laevis</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc9LwzAUx4Moc07vXoQexNM6kzZtWm8y_DEQ5mHCToY0fVkzumYmmbL_3uiGB0F88HiH9_1-efkEoXOCRwQzer2s5Chh6YjSUVLkGTtAfYKLNE4zMj9EfYwTEpdJVhyjE-eWOBQtSQ_1SlbkRVb20eusgei52TptWrPQMhqbTkLnrfDadJFR0aQzTnvTRmRIh1k8s9qtGxNaeIh0F_kQMDVy68F9yefQmfXGRa2Ad-1O0ZESrYOz_Rygl_u72fgxfpo-TMa3T7GklPk4U1UqiEooxjUkBStpLSUWsgalmBQQ3iohZ2kuS8VIUilWkQJXLKO5wEWVpQN0tctdW_O2Aef5SjsJbSs6MBvH8zIUDQn_CQnDZSCJgxDvhNIa5ywovrZ6JeyWE8y_2PPAngf2nFL-zT5YLvbZm2oF9Y9hDzvsL3f7Ri-aD22BV9rIBla_Y252MgjA3jVY7qSG8Ct1sEjPa6P_vuET-Gmfsw</recordid><startdate>19981030</startdate><enddate>19981030</enddate><creator>Luzzi, Veronica</creator><creator>Sims, Christopher E.</creator><creator>Soughayer, Joseph S.</creator><creator>Allbritton, Nancy L.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</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>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>19981030</creationdate><title>The Physiologic Concentration of Inositol 1,4,5-Trisphosphate in the Oocytes of Xenopus laevis</title><author>Luzzi, Veronica ; Sims, Christopher E. ; Soughayer, Joseph S. ; Allbritton, Nancy L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c447t-5fb3a1f2400de28794dcc0acdeff7cae107ce6736c9f712bf7b180b7546a08b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Calcium Signaling</topic><topic>Cell Line</topic><topic>Electrophoresis, Capillary</topic><topic>Freshwater</topic><topic>Guinea Pigs</topic><topic>Inositol 1,4,5-Trisphosphate - metabolism</topic><topic>Inositol 1,4,5-Trisphosphate - physiology</topic><topic>Oocytes - metabolism</topic><topic>Oocytes - physiology</topic><topic>PC12 Cells</topic><topic>Rats</topic><topic>Spectrometry, Fluorescence</topic><topic>Xenopus laevis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luzzi, Veronica</creatorcontrib><creatorcontrib>Sims, Christopher E.</creatorcontrib><creatorcontrib>Soughayer, Joseph S.</creatorcontrib><creatorcontrib>Allbritton, Nancy L.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luzzi, Veronica</au><au>Sims, Christopher E.</au><au>Soughayer, Joseph S.</au><au>Allbritton, Nancy L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Physiologic Concentration of Inositol 1,4,5-Trisphosphate in the Oocytes of Xenopus laevis</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>1998-10-30</date><risdate>1998</risdate><volume>273</volume><issue>44</issue><spage>28657</spage><epage>28662</epage><pages>28657-28662</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>To measure the concentration of inositol 1,4,5-trisphosphate ([IP3]) in small regions of single Xenopus oocytes, a biological detector cell was combined with capillary electrophoresis. This method is 10,000 times more sensitive than all existing assays enabling subcellular measurement of [IP3] in Xenopus oocytes. Upon addition of lysophosphatidic acid to an oocyte, [IP3] increased from 40 to 650 nm within 2 min. IP3concentrations as high as 1.8 μm were measured after activation with lysophosphatidic acid, suggesting that the physiologic concentration of IP3 ranges from the tens of nanomolar to a few micromolar in Xenopus oocytes. Since the IP3 receptor in Xenopus oocytes is nearly identical to the type I receptor of mammalian cells, the range of [IP3] in most mammalian cells is likely to be similar to that in the oocyte. By selecting or engineering the appropriate detector cell, this strategy should be applicable to cyclic adenosine diphosphate ribose and nicotinic acid adenine dinucleotide phosphate, and to the discovery of new Ca2+-releasing second messengers.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>9786859</pmid><doi>10.1074/jbc.273.44.28657</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Calcium Signaling Cell Line Electrophoresis, Capillary Freshwater Guinea Pigs Inositol 1,4,5-Trisphosphate - metabolism Inositol 1,4,5-Trisphosphate - physiology Oocytes - metabolism Oocytes - physiology PC12 Cells Rats Spectrometry, Fluorescence Xenopus laevis |
title | The Physiologic Concentration of Inositol 1,4,5-Trisphosphate in the Oocytes of Xenopus laevis |
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