Phospholipids and Their Derivatives as Mitogen and Motogen of Budding Tunicates
In order to discover novel invertebrate cytokines from the budding tunicate, Polyandrocarpa misakiensis, we treated the water-insoluble fraction of tunicate homogenates with trypsin. The extracts showed remarkable activities to promote the growth and motility of tunicate cells. The activities were h...
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Veröffentlicht in: | Journal of biochemistry (Tokyo) 2004-01, Vol.135 (1), p.71-78 |
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description | In order to discover novel invertebrate cytokines from the budding tunicate, Polyandrocarpa misakiensis, we treated the water-insoluble fraction of tunicate homogenates with trypsin. The extracts showed remarkable activities to promote the growth and motility of tunicate cells. The activities were heat-stable and proteinase K-resistant. After anion exchange chromatography, the activities were eluted with detergents such as 0.1% deoxycholic acid. The Fourier transform infrared spectrum indicated large amounts of fatty acids and phospholipids instead of polypeptides in the extracts. Consistently, the activities were extractable with organic solvents such as chloroform. Long chains of n-3 polyunsaturated free fatty acids (FFA), phosphatidylinositol (PI), phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylserine (PS) were the major components in the lipid-soluble fraction. A cDNA for FFA-releasing enzyme phospholipase A2 (PLA2) was cloned. The expression of this gene could be seen in epidermal cells during budding. The recombinant protein, as in the case of the authentic PLA2, preferred PC and PE as substrates, followed by PS and PI. The resultant FFAs only promoted cell growth, while the remaining lysophospholipids stimulated cell motility. The former contained unsaturated fatty acids (C18:1, C20:5, and C22:6) while the latter did not, suggesting that unsaturated fatty acids are responsible for mitogenic activity in tunicate cells. These results show for the first time that phospholipids and their derivatives are bio-mediators promoting cell growth and cell motility in invertebrates. |
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The extracts showed remarkable activities to promote the growth and motility of tunicate cells. The activities were heat-stable and proteinase K-resistant. After anion exchange chromatography, the activities were eluted with detergents such as 0.1% deoxycholic acid. The Fourier transform infrared spectrum indicated large amounts of fatty acids and phospholipids instead of polypeptides in the extracts. Consistently, the activities were extractable with organic solvents such as chloroform. Long chains of n-3 polyunsaturated free fatty acids (FFA), phosphatidylinositol (PI), phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylserine (PS) were the major components in the lipid-soluble fraction. A cDNA for FFA-releasing enzyme phospholipase A2 (PLA2) was cloned. The expression of this gene could be seen in epidermal cells during budding. The recombinant protein, as in the case of the authentic PLA2, preferred PC and PE as substrates, followed by PS and PI. The resultant FFAs only promoted cell growth, while the remaining lysophospholipids stimulated cell motility. The former contained unsaturated fatty acids (C18:1, C20:5, and C22:6) while the latter did not, suggesting that unsaturated fatty acids are responsible for mitogenic activity in tunicate cells. These results show for the first time that phospholipids and their derivatives are bio-mediators promoting cell growth and cell motility in invertebrates.</description><identifier>ISSN: 0021-924X</identifier><identifier>DOI: 10.1093/jb/mvh008</identifier><identifier>PMID: 14999011</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Amino Acid Sequence ; Animals ; budding ; cell growth ; cell motility ; Cell Movement - drug effects ; Cell Movement - genetics ; Cell-Free System - physiology ; Cells, Cultured ; fatty acid ; Mitogens - genetics ; Mitogens - isolation & purification ; Mitogens - pharmacology ; Molecular Sequence Data ; phospholipase A2 ; phospholipid ; Phospholipids - genetics ; Phospholipids - isolation & purification ; Phospholipids - pharmacology ; tunicate ; Urochordata - cytology ; Urochordata - genetics ; Urochordata - growth & development</subject><ispartof>Journal of biochemistry (Tokyo), 2004-01, Vol.135 (1), p.71-78</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-4069239f032d8ac40eb33a7ea032b22b8f222238f73aec3741e0daa4aeb659a93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14999011$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arai, Kazuya</creatorcontrib><creatorcontrib>Yoshida, Satoshi</creatorcontrib><creatorcontrib>Nakatani, Masanao</creatorcontrib><creatorcontrib>Fujiwara, Shigeki</creatorcontrib><creatorcontrib>Yubisui, Toshitsugu</creatorcontrib><creatorcontrib>Kawamura, Kazuo</creatorcontrib><title>Phospholipids and Their Derivatives as Mitogen and Motogen of Budding Tunicates</title><title>Journal of biochemistry (Tokyo)</title><addtitle>J Biochem</addtitle><description>In order to discover novel invertebrate cytokines from the budding tunicate, Polyandrocarpa misakiensis, we treated the water-insoluble fraction of tunicate homogenates with trypsin. The extracts showed remarkable activities to promote the growth and motility of tunicate cells. The activities were heat-stable and proteinase K-resistant. After anion exchange chromatography, the activities were eluted with detergents such as 0.1% deoxycholic acid. The Fourier transform infrared spectrum indicated large amounts of fatty acids and phospholipids instead of polypeptides in the extracts. Consistently, the activities were extractable with organic solvents such as chloroform. Long chains of n-3 polyunsaturated free fatty acids (FFA), phosphatidylinositol (PI), phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylserine (PS) were the major components in the lipid-soluble fraction. A cDNA for FFA-releasing enzyme phospholipase A2 (PLA2) was cloned. The expression of this gene could be seen in epidermal cells during budding. The recombinant protein, as in the case of the authentic PLA2, preferred PC and PE as substrates, followed by PS and PI. The resultant FFAs only promoted cell growth, while the remaining lysophospholipids stimulated cell motility. The former contained unsaturated fatty acids (C18:1, C20:5, and C22:6) while the latter did not, suggesting that unsaturated fatty acids are responsible for mitogenic activity in tunicate cells. These results show for the first time that phospholipids and their derivatives are bio-mediators promoting cell growth and cell motility in invertebrates.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>budding</subject><subject>cell growth</subject><subject>cell motility</subject><subject>Cell Movement - drug effects</subject><subject>Cell Movement - genetics</subject><subject>Cell-Free System - physiology</subject><subject>Cells, Cultured</subject><subject>fatty acid</subject><subject>Mitogens - genetics</subject><subject>Mitogens - isolation & purification</subject><subject>Mitogens - pharmacology</subject><subject>Molecular Sequence Data</subject><subject>phospholipase A2</subject><subject>phospholipid</subject><subject>Phospholipids - genetics</subject><subject>Phospholipids - isolation & purification</subject><subject>Phospholipids - pharmacology</subject><subject>tunicate</subject><subject>Urochordata - cytology</subject><subject>Urochordata - genetics</subject><subject>Urochordata - growth & development</subject><issn>0021-924X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtPg0AUhWehsbW68A8YViYusPOgwCx9tsY2dYFN42YywKVMBQZnoNF_L5VG7-bec-6XszgIXRB8QzBn4208Lnc5xuERGmJMicuptx6gU2u3e0kZO0ED4nHOMSFDtHzNta1zXahapdaRVepEOSjjPIBRO9moHXSudRaq0RuofoGF7m-dOXdtmqpq40RtpRLZgD1Dx5ksLJwf9gi9PT1G9zN3vpw-39_O3YSFk8b1sM8p4xlmNA1l4mGIGZMByM6IKY3DjHbDwixgEhIWeARwKqUnIfYnXHI2Qld9bm30Zwu2EaWyCRSFrEC3VgTE5x5nQQde92BitLUGMlEbVUrzLQgW-8bENhZ9Yx17eQht4xLSf_JQVwe4PaBsA19_f2k-hB-wYCJm63fxMvWj1XQVCsJ-AMhmeJY</recordid><startdate>200401</startdate><enddate>200401</enddate><creator>Arai, Kazuya</creator><creator>Yoshida, Satoshi</creator><creator>Nakatani, Masanao</creator><creator>Fujiwara, Shigeki</creator><creator>Yubisui, Toshitsugu</creator><creator>Kawamura, Kazuo</creator><general>Oxford University Press</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>200401</creationdate><title>Phospholipids and Their Derivatives as Mitogen and Motogen of Budding Tunicates</title><author>Arai, Kazuya ; Yoshida, Satoshi ; Nakatani, Masanao ; Fujiwara, Shigeki ; Yubisui, Toshitsugu ; Kawamura, Kazuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-4069239f032d8ac40eb33a7ea032b22b8f222238f73aec3741e0daa4aeb659a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>budding</topic><topic>cell growth</topic><topic>cell motility</topic><topic>Cell Movement - drug effects</topic><topic>Cell Movement - genetics</topic><topic>Cell-Free System - physiology</topic><topic>Cells, Cultured</topic><topic>fatty acid</topic><topic>Mitogens - genetics</topic><topic>Mitogens - isolation & purification</topic><topic>Mitogens - pharmacology</topic><topic>Molecular Sequence Data</topic><topic>phospholipase A2</topic><topic>phospholipid</topic><topic>Phospholipids - genetics</topic><topic>Phospholipids - isolation & purification</topic><topic>Phospholipids - pharmacology</topic><topic>tunicate</topic><topic>Urochordata - cytology</topic><topic>Urochordata - genetics</topic><topic>Urochordata - growth & development</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arai, Kazuya</creatorcontrib><creatorcontrib>Yoshida, Satoshi</creatorcontrib><creatorcontrib>Nakatani, Masanao</creatorcontrib><creatorcontrib>Fujiwara, Shigeki</creatorcontrib><creatorcontrib>Yubisui, Toshitsugu</creatorcontrib><creatorcontrib>Kawamura, Kazuo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biochemistry (Tokyo)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arai, Kazuya</au><au>Yoshida, Satoshi</au><au>Nakatani, Masanao</au><au>Fujiwara, Shigeki</au><au>Yubisui, Toshitsugu</au><au>Kawamura, Kazuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phospholipids and Their Derivatives as Mitogen and Motogen of Budding Tunicates</atitle><jtitle>Journal of biochemistry (Tokyo)</jtitle><addtitle>J Biochem</addtitle><date>2004-01</date><risdate>2004</risdate><volume>135</volume><issue>1</issue><spage>71</spage><epage>78</epage><pages>71-78</pages><issn>0021-924X</issn><abstract>In order to discover novel invertebrate cytokines from the budding tunicate, Polyandrocarpa misakiensis, we treated the water-insoluble fraction of tunicate homogenates with trypsin. The extracts showed remarkable activities to promote the growth and motility of tunicate cells. The activities were heat-stable and proteinase K-resistant. After anion exchange chromatography, the activities were eluted with detergents such as 0.1% deoxycholic acid. The Fourier transform infrared spectrum indicated large amounts of fatty acids and phospholipids instead of polypeptides in the extracts. Consistently, the activities were extractable with organic solvents such as chloroform. Long chains of n-3 polyunsaturated free fatty acids (FFA), phosphatidylinositol (PI), phosphatidylcholine (PC), phosphatidylethanolamine (PE) and phosphatidylserine (PS) were the major components in the lipid-soluble fraction. A cDNA for FFA-releasing enzyme phospholipase A2 (PLA2) was cloned. The expression of this gene could be seen in epidermal cells during budding. The recombinant protein, as in the case of the authentic PLA2, preferred PC and PE as substrates, followed by PS and PI. The resultant FFAs only promoted cell growth, while the remaining lysophospholipids stimulated cell motility. The former contained unsaturated fatty acids (C18:1, C20:5, and C22:6) while the latter did not, suggesting that unsaturated fatty acids are responsible for mitogenic activity in tunicate cells. These results show for the first time that phospholipids and their derivatives are bio-mediators promoting cell growth and cell motility in invertebrates.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>14999011</pmid><doi>10.1093/jb/mvh008</doi><tpages>8</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals budding cell growth cell motility Cell Movement - drug effects Cell Movement - genetics Cell-Free System - physiology Cells, Cultured fatty acid Mitogens - genetics Mitogens - isolation & purification Mitogens - pharmacology Molecular Sequence Data phospholipase A2 phospholipid Phospholipids - genetics Phospholipids - isolation & purification Phospholipids - pharmacology tunicate Urochordata - cytology Urochordata - genetics Urochordata - growth & development |
title | Phospholipids and Their Derivatives as Mitogen and Motogen of Budding Tunicates |
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