Effects of Docosahexaenoic and Arachidonic Acids on the Synthesis and Distribution of Aminophospholipids during Neuronal Differentiation of PC12 Cells
We have shown previously that docosahexaenoic acid (DHA) promotes and arachidonic acid (AA) suppresses neurite outgrowth of PC12 cells induced by nerve growth factor (NGF) and that incorporation of [3H]ethanolamine into phosphatidylethanolamine (PE) is suppressed in PC12 cells by AA while DHA has no...
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description | We have shown previously that docosahexaenoic acid (DHA) promotes and arachidonic acid (AA) suppresses neurite outgrowth of PC12 cells induced by nerve growth factor (NGF) and that incorporation of [3H]ethanolamine into phosphatidylethanolamine (PE) is suppressed in PC12 cells by AA while DHA has no effect. In the present study, the effects of these fatty acids on PE synthesis via decarboxylation of phosphatidylserine (PS), another pathway of PE synthesis, and distribution of aminophospholipids were examined. Incorporation of [3H]serine into PS and PE was elevated in the course of NGF-induced differentiation and was further stimulated significantly by DHA, but not by AA. [3H]Ethanolamine uptake by PC12 cells was significantly suppressed by AA but not by DHA while these fatty acids did not affect [3H]serine uptake, indicating that the suppression by AA of [3H]ethanolamine incorporation into phosphatidylethanolamine is attributable, at least in part, to a reduction in [3H]ethanolamine uptake. The distribution of PE in the outer leaflet of plasma membrane decreased during differentiation, which is known to be accompanied by an increase in the surface area of plasma membrane. Supplementation of PC12 cells with DHA or AA did not affect the distribution of aminophospholipids. Thus, DHA and AA affected aminophospholipid synthesis and neurite outgrowth differently, but not the transport and distribution of aminophospholipids, while the PE concentration in the outer leaflet of the plasma membrane decreased in association with morphological changes in PC12 cells induced by NGF. |
doi_str_mv | 10.1006/abbi.1999.1110 |
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In the present study, the effects of these fatty acids on PE synthesis via decarboxylation of phosphatidylserine (PS), another pathway of PE synthesis, and distribution of aminophospholipids were examined. Incorporation of [3H]serine into PS and PE was elevated in the course of NGF-induced differentiation and was further stimulated significantly by DHA, but not by AA. [3H]Ethanolamine uptake by PC12 cells was significantly suppressed by AA but not by DHA while these fatty acids did not affect [3H]serine uptake, indicating that the suppression by AA of [3H]ethanolamine incorporation into phosphatidylethanolamine is attributable, at least in part, to a reduction in [3H]ethanolamine uptake. The distribution of PE in the outer leaflet of plasma membrane decreased during differentiation, which is known to be accompanied by an increase in the surface area of plasma membrane. Supplementation of PC12 cells with DHA or AA did not affect the distribution of aminophospholipids. Thus, DHA and AA affected aminophospholipid synthesis and neurite outgrowth differently, but not the transport and distribution of aminophospholipids, while the PE concentration in the outer leaflet of the plasma membrane decreased in association with morphological changes in PC12 cells induced by NGF.</description><identifier>ISSN: 0003-9861</identifier><identifier>EISSN: 1096-0384</identifier><identifier>DOI: 10.1006/abbi.1999.1110</identifier><identifier>PMID: 10087166</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Anti-Bacterial Agents - metabolism ; arachidonic acid ; Arachidonic Acid - pharmacology ; Cell Differentiation ; Cell Membrane - metabolism ; Cell Size - drug effects ; docosahexaenoic acid ; Docosahexaenoic Acids - pharmacology ; Ethanolamine - metabolism ; Flow Cytometry ; Hemolysin Proteins - metabolism ; nerve growth factor ; Nerve Growth Factors - pharmacology ; Neurons - drug effects ; Neurons - metabolism ; PC12 Cells ; Peptides ; phosphatidylethanolamine ; Phosphatidylethanolamines - metabolism ; phosphatidylserine ; Phosphatidylserines - metabolism ; phospholipids ; Phospholipids - metabolism ; polyunsaturated fatty acids ; Rats ; Serine - metabolism ; Trinitrobenzenesulfonic Acid - metabolism ; Tritium</subject><ispartof>Archives of biochemistry and biophysics, 1999-04, Vol.364 (1), p.67-74</ispartof><rights>1999 Academic Press</rights><rights>Copyright 1999 Academic Press.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-a50a6ba824b058e604b628742e2d7f3e1ef6b6f9bf8ac4f6fb07180128b216043</citedby><cites>FETCH-LOGICAL-c430t-a50a6ba824b058e604b628742e2d7f3e1ef6b6f9bf8ac4f6fb07180128b216043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/abbi.1999.1110$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10087166$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ikemoto, Atsushi</creatorcontrib><creatorcontrib>Kobayashi, Tetsuyuki</creatorcontrib><creatorcontrib>Emoto, Kazuo</creatorcontrib><creatorcontrib>Umeda, Masato</creatorcontrib><creatorcontrib>Watanabe, Shiro</creatorcontrib><creatorcontrib>Okuyama, Harumi</creatorcontrib><title>Effects of Docosahexaenoic and Arachidonic Acids on the Synthesis and Distribution of Aminophospholipids during Neuronal Differentiation of PC12 Cells</title><title>Archives of biochemistry and biophysics</title><addtitle>Arch Biochem Biophys</addtitle><description>We have shown previously that docosahexaenoic acid (DHA) promotes and arachidonic acid (AA) suppresses neurite outgrowth of PC12 cells induced by nerve growth factor (NGF) and that incorporation of [3H]ethanolamine into phosphatidylethanolamine (PE) is suppressed in PC12 cells by AA while DHA has no effect. In the present study, the effects of these fatty acids on PE synthesis via decarboxylation of phosphatidylserine (PS), another pathway of PE synthesis, and distribution of aminophospholipids were examined. Incorporation of [3H]serine into PS and PE was elevated in the course of NGF-induced differentiation and was further stimulated significantly by DHA, but not by AA. [3H]Ethanolamine uptake by PC12 cells was significantly suppressed by AA but not by DHA while these fatty acids did not affect [3H]serine uptake, indicating that the suppression by AA of [3H]ethanolamine incorporation into phosphatidylethanolamine is attributable, at least in part, to a reduction in [3H]ethanolamine uptake. The distribution of PE in the outer leaflet of plasma membrane decreased during differentiation, which is known to be accompanied by an increase in the surface area of plasma membrane. Supplementation of PC12 cells with DHA or AA did not affect the distribution of aminophospholipids. Thus, DHA and AA affected aminophospholipid synthesis and neurite outgrowth differently, but not the transport and distribution of aminophospholipids, while the PE concentration in the outer leaflet of the plasma membrane decreased in association with morphological changes in PC12 cells induced by NGF.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - metabolism</subject><subject>arachidonic acid</subject><subject>Arachidonic Acid - pharmacology</subject><subject>Cell Differentiation</subject><subject>Cell Membrane - metabolism</subject><subject>Cell Size - drug effects</subject><subject>docosahexaenoic acid</subject><subject>Docosahexaenoic Acids - pharmacology</subject><subject>Ethanolamine - metabolism</subject><subject>Flow Cytometry</subject><subject>Hemolysin Proteins - metabolism</subject><subject>nerve growth factor</subject><subject>Nerve Growth Factors - pharmacology</subject><subject>Neurons - drug effects</subject><subject>Neurons - metabolism</subject><subject>PC12 Cells</subject><subject>Peptides</subject><subject>phosphatidylethanolamine</subject><subject>Phosphatidylethanolamines - metabolism</subject><subject>phosphatidylserine</subject><subject>Phosphatidylserines - metabolism</subject><subject>phospholipids</subject><subject>Phospholipids - metabolism</subject><subject>polyunsaturated fatty acids</subject><subject>Rats</subject><subject>Serine - metabolism</subject><subject>Trinitrobenzenesulfonic Acid - metabolism</subject><subject>Tritium</subject><issn>0003-9861</issn><issn>1096-0384</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU9v1DAQxS0EokvhyhFy4pZl7KSOc1xtyx-pAqTSs2U74-6grL3YCaJfhM-LQ4rEhYM1sub33ozmMfaSw5YDyLfGWtryvu-3nHN4xDYcellDo9rHbAMATd0ryc_Ys5y_AXDeSvGUnRWp6riUG_brynt0U66iry6ji9kc8KfBEMlVJgzVLhl3oCGG8t85GgoYqumA1c19KCVT_oNdUp4S2Xmi0i5WuyOFeDrEXN5Ip0U3zInCXfUJ5xSDGYukTE4YJjJ_VV_2XFR7HMf8nD3xZsz44qGes9t3V1_3H-rrz-8_7nfXtWsbmGpzAUZao0Rr4UKhhNZKobpWoBg63yBHL630vfXKuNZLb6HjCrhQVvBCN-fszep7SvH7jHnSR8qubGACxjlr2csWmk4WcLuCLsWcE3p9SnQ06V5z0EsSeklCL0noJYkiePXgPNsjDv_g6-kL8HoFvIna3CXK-vZGAG9AqL4TvSqEWgksF_hBmHR2hMHhQKlkpodI_5v-Gy--otM</recordid><startdate>19990401</startdate><enddate>19990401</enddate><creator>Ikemoto, Atsushi</creator><creator>Kobayashi, Tetsuyuki</creator><creator>Emoto, Kazuo</creator><creator>Umeda, Masato</creator><creator>Watanabe, Shiro</creator><creator>Okuyama, Harumi</creator><general>Elsevier Inc</general><scope>FBQ</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>19990401</creationdate><title>Effects of Docosahexaenoic and Arachidonic Acids on the Synthesis and Distribution of Aminophospholipids during Neuronal Differentiation of PC12 Cells</title><author>Ikemoto, Atsushi ; Kobayashi, Tetsuyuki ; Emoto, Kazuo ; Umeda, Masato ; Watanabe, Shiro ; Okuyama, Harumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-a50a6ba824b058e604b628742e2d7f3e1ef6b6f9bf8ac4f6fb07180128b216043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - metabolism</topic><topic>arachidonic acid</topic><topic>Arachidonic Acid - pharmacology</topic><topic>Cell Differentiation</topic><topic>Cell Membrane - metabolism</topic><topic>Cell Size - drug effects</topic><topic>docosahexaenoic acid</topic><topic>Docosahexaenoic Acids - pharmacology</topic><topic>Ethanolamine - metabolism</topic><topic>Flow Cytometry</topic><topic>Hemolysin Proteins - metabolism</topic><topic>nerve growth factor</topic><topic>Nerve Growth Factors - pharmacology</topic><topic>Neurons - drug effects</topic><topic>Neurons - metabolism</topic><topic>PC12 Cells</topic><topic>Peptides</topic><topic>phosphatidylethanolamine</topic><topic>Phosphatidylethanolamines - metabolism</topic><topic>phosphatidylserine</topic><topic>Phosphatidylserines - metabolism</topic><topic>phospholipids</topic><topic>Phospholipids - metabolism</topic><topic>polyunsaturated fatty acids</topic><topic>Rats</topic><topic>Serine - metabolism</topic><topic>Trinitrobenzenesulfonic Acid - metabolism</topic><topic>Tritium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ikemoto, Atsushi</creatorcontrib><creatorcontrib>Kobayashi, Tetsuyuki</creatorcontrib><creatorcontrib>Emoto, Kazuo</creatorcontrib><creatorcontrib>Umeda, Masato</creatorcontrib><creatorcontrib>Watanabe, Shiro</creatorcontrib><creatorcontrib>Okuyama, Harumi</creatorcontrib><collection>AGRIS</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>Archives of biochemistry and biophysics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ikemoto, Atsushi</au><au>Kobayashi, Tetsuyuki</au><au>Emoto, Kazuo</au><au>Umeda, Masato</au><au>Watanabe, Shiro</au><au>Okuyama, Harumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of Docosahexaenoic and Arachidonic Acids on the Synthesis and Distribution of Aminophospholipids during Neuronal Differentiation of PC12 Cells</atitle><jtitle>Archives of biochemistry and biophysics</jtitle><addtitle>Arch Biochem Biophys</addtitle><date>1999-04-01</date><risdate>1999</risdate><volume>364</volume><issue>1</issue><spage>67</spage><epage>74</epage><pages>67-74</pages><issn>0003-9861</issn><eissn>1096-0384</eissn><abstract>We have shown previously that docosahexaenoic acid (DHA) promotes and arachidonic acid (AA) suppresses neurite outgrowth of PC12 cells induced by nerve growth factor (NGF) and that incorporation of [3H]ethanolamine into phosphatidylethanolamine (PE) is suppressed in PC12 cells by AA while DHA has no effect. In the present study, the effects of these fatty acids on PE synthesis via decarboxylation of phosphatidylserine (PS), another pathway of PE synthesis, and distribution of aminophospholipids were examined. Incorporation of [3H]serine into PS and PE was elevated in the course of NGF-induced differentiation and was further stimulated significantly by DHA, but not by AA. [3H]Ethanolamine uptake by PC12 cells was significantly suppressed by AA but not by DHA while these fatty acids did not affect [3H]serine uptake, indicating that the suppression by AA of [3H]ethanolamine incorporation into phosphatidylethanolamine is attributable, at least in part, to a reduction in [3H]ethanolamine uptake. The distribution of PE in the outer leaflet of plasma membrane decreased during differentiation, which is known to be accompanied by an increase in the surface area of plasma membrane. Supplementation of PC12 cells with DHA or AA did not affect the distribution of aminophospholipids. Thus, DHA and AA affected aminophospholipid synthesis and neurite outgrowth differently, but not the transport and distribution of aminophospholipids, while the PE concentration in the outer leaflet of the plasma membrane decreased in association with morphological changes in PC12 cells induced by NGF.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10087166</pmid><doi>10.1006/abbi.1999.1110</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Anti-Bacterial Agents - metabolism arachidonic acid Arachidonic Acid - pharmacology Cell Differentiation Cell Membrane - metabolism Cell Size - drug effects docosahexaenoic acid Docosahexaenoic Acids - pharmacology Ethanolamine - metabolism Flow Cytometry Hemolysin Proteins - metabolism nerve growth factor Nerve Growth Factors - pharmacology Neurons - drug effects Neurons - metabolism PC12 Cells Peptides phosphatidylethanolamine Phosphatidylethanolamines - metabolism phosphatidylserine Phosphatidylserines - metabolism phospholipids Phospholipids - metabolism polyunsaturated fatty acids Rats Serine - metabolism Trinitrobenzenesulfonic Acid - metabolism Tritium |
title | Effects of Docosahexaenoic and Arachidonic Acids on the Synthesis and Distribution of Aminophospholipids during Neuronal Differentiation of PC12 Cells |
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