Differential expression of phospholipase D1 in the developing retina
Expression patterns of phospholipase D1 (PLD1) in the developing rat retina were investigated using immunocytochemistry and Western blot analysis and compared with the expression patterns of glutamine synthetase. PLD1 immunoreactivity appeared first in a few neuroblasts in the middle of the mantle z...
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Veröffentlicht in: | The European journal of neuroscience 2002-03, Vol.15 (6), p.1006-1012 |
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description | Expression patterns of phospholipase D1 (PLD1) in the developing rat retina were investigated using immunocytochemistry and Western blot analysis and compared with the expression patterns of glutamine synthetase. PLD1 immunoreactivity appeared first in a few neuroblasts in the middle of the mantle zone of the primitive retina by embryonic (E) day 13. PLD1‐immunoreactive primitive ganglion cells were characterized in the ganglion cell layer by E17. Faint immunoreactivity at E17 profiled radially orientated cells and this pattern appeared up to postnatal (P) day 7. In the ganglion cell layer at P3, displaced amacrine cells and ganglion cells were classified. At P5, presumptive horizontal cells and amacrine cells were identified. By P7, a thin outermost layer of newly formed segments of the photoreceptor cells was also PLD1 immunoreactive. PLD1 immunoreactivity at P8 was limited to radial Müller cells and the outer segment layer of the photoreceptor cells, and the expression pattern was conserved to adulthood. Western blot analysis showed relatively high amounts of PLD1 protein at E17 and P3, a decrease at P7, and moderate amounts from P8 onward. Co‐expression of PLD1 with glutamine synthetase in the retina appeared first after birth in differentiating neurons and in Müller cells by P8; thereafter the pattern was maintained. The expression pattern of the PLD1 during development of the retina suggests that PLD1 plays important roles in glutamate‐associated differentiation of both specific neurons and radial glial cells, and in glutamate‐mediated cellular signalling in Müller cells. |
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S. ; Lee, M.-Y. ; Chung, J.-W. ; Chun, M.-H. ; Oh, S.-J.</creator><creatorcontrib>Lee, E.-J. ; Min, D. S. ; Lee, M.-Y. ; Chung, J.-W. ; Chun, M.-H. ; Oh, S.-J.</creatorcontrib><description>Expression patterns of phospholipase D1 (PLD1) in the developing rat retina were investigated using immunocytochemistry and Western blot analysis and compared with the expression patterns of glutamine synthetase. PLD1 immunoreactivity appeared first in a few neuroblasts in the middle of the mantle zone of the primitive retina by embryonic (E) day 13. PLD1‐immunoreactive primitive ganglion cells were characterized in the ganglion cell layer by E17. Faint immunoreactivity at E17 profiled radially orientated cells and this pattern appeared up to postnatal (P) day 7. In the ganglion cell layer at P3, displaced amacrine cells and ganglion cells were classified. At P5, presumptive horizontal cells and amacrine cells were identified. By P7, a thin outermost layer of newly formed segments of the photoreceptor cells was also PLD1 immunoreactive. PLD1 immunoreactivity at P8 was limited to radial Müller cells and the outer segment layer of the photoreceptor cells, and the expression pattern was conserved to adulthood. Western blot analysis showed relatively high amounts of PLD1 protein at E17 and P3, a decrease at P7, and moderate amounts from P8 onward. Co‐expression of PLD1 with glutamine synthetase in the retina appeared first after birth in differentiating neurons and in Müller cells by P8; thereafter the pattern was maintained. The expression pattern of the PLD1 during development of the retina suggests that PLD1 plays important roles in glutamate‐associated differentiation of both specific neurons and radial glial cells, and in glutamate‐mediated cellular signalling in Müller cells.</description><identifier>ISSN: 0953-816X</identifier><identifier>EISSN: 1460-9568</identifier><identifier>DOI: 10.1046/j.1460-9568.2002.01939.x</identifier><identifier>PMID: 11918661</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science, Ltd</publisher><subject>Aging - metabolism ; Animals ; Animals, Newborn ; Cell Differentiation - physiology ; Cell Lineage - physiology ; differentiation ; Female ; Fetus ; Glutamate-Ammonia Ligase - metabolism ; Glutamic Acid - metabolism ; glutamine synthetase ; immunocytochemistry ; Immunohistochemistry ; Microtubule-Associated Proteins - metabolism ; Neuroglia - cytology ; Neuroglia - enzymology ; Neurons - cytology ; Neurons - enzymology ; Phospholipase D - metabolism ; Pregnancy ; rat ; Rats ; Rats, Sprague-Dawley ; Retina - embryology ; Retina - enzymology ; Retina - growth & development ; Signal Transduction - physiology ; Stem Cells - cytology ; Stem Cells - enzymology ; Western blot analysis</subject><ispartof>The European journal of neuroscience, 2002-03, Vol.15 (6), p.1006-1012</ispartof><rights>Federation of European Neuroscience Societies</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5029-da75956374d8e41da6d4cbbdff133790c1a3ef187414987ea300d0dda87ace3a3</citedby><cites>FETCH-LOGICAL-c5029-da75956374d8e41da6d4cbbdff133790c1a3ef187414987ea300d0dda87ace3a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1460-9568.2002.01939.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1460-9568.2002.01939.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11918661$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, E.-J.</creatorcontrib><creatorcontrib>Min, D. S.</creatorcontrib><creatorcontrib>Lee, M.-Y.</creatorcontrib><creatorcontrib>Chung, J.-W.</creatorcontrib><creatorcontrib>Chun, M.-H.</creatorcontrib><creatorcontrib>Oh, S.-J.</creatorcontrib><title>Differential expression of phospholipase D1 in the developing retina</title><title>The European journal of neuroscience</title><addtitle>Eur J Neurosci</addtitle><description>Expression patterns of phospholipase D1 (PLD1) in the developing rat retina were investigated using immunocytochemistry and Western blot analysis and compared with the expression patterns of glutamine synthetase. PLD1 immunoreactivity appeared first in a few neuroblasts in the middle of the mantle zone of the primitive retina by embryonic (E) day 13. PLD1‐immunoreactive primitive ganglion cells were characterized in the ganglion cell layer by E17. Faint immunoreactivity at E17 profiled radially orientated cells and this pattern appeared up to postnatal (P) day 7. In the ganglion cell layer at P3, displaced amacrine cells and ganglion cells were classified. At P5, presumptive horizontal cells and amacrine cells were identified. By P7, a thin outermost layer of newly formed segments of the photoreceptor cells was also PLD1 immunoreactive. PLD1 immunoreactivity at P8 was limited to radial Müller cells and the outer segment layer of the photoreceptor cells, and the expression pattern was conserved to adulthood. Western blot analysis showed relatively high amounts of PLD1 protein at E17 and P3, a decrease at P7, and moderate amounts from P8 onward. Co‐expression of PLD1 with glutamine synthetase in the retina appeared first after birth in differentiating neurons and in Müller cells by P8; thereafter the pattern was maintained. The expression pattern of the PLD1 during development of the retina suggests that PLD1 plays important roles in glutamate‐associated differentiation of both specific neurons and radial glial cells, and in glutamate‐mediated cellular signalling in Müller cells.</description><subject>Aging - metabolism</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Lineage - physiology</subject><subject>differentiation</subject><subject>Female</subject><subject>Fetus</subject><subject>Glutamate-Ammonia Ligase - metabolism</subject><subject>Glutamic Acid - metabolism</subject><subject>glutamine synthetase</subject><subject>immunocytochemistry</subject><subject>Immunohistochemistry</subject><subject>Microtubule-Associated Proteins - metabolism</subject><subject>Neuroglia - cytology</subject><subject>Neuroglia - enzymology</subject><subject>Neurons - cytology</subject><subject>Neurons - enzymology</subject><subject>Phospholipase D - metabolism</subject><subject>Pregnancy</subject><subject>rat</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Retina - embryology</subject><subject>Retina - enzymology</subject><subject>Retina - growth & development</subject><subject>Signal Transduction - physiology</subject><subject>Stem Cells - cytology</subject><subject>Stem Cells - enzymology</subject><subject>Western blot analysis</subject><issn>0953-816X</issn><issn>1460-9568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkM9v0zAUgC0EYmXwLyCfEJeE9-rEPw4coN3G0DQkNGA3y41fmEuaBDuF7r8nWavtNnGwbMnf92x9jHGEHKGQ79Y5FhIyU0qdzwHmOaARJt89YbP7i6dsBqYUmUZ5fcRepLQGAC2L8jk7QjSopcQZWy5DXVOkdgiu4bTrI6UUupZ3Ne9vujSuJvQuEV8iDy0fboh7-kNN14f2J480hNa9ZM9q1yR6ddiP2bfTk6vFp-ziy9n54sNFVpUwN5l3qhx_JlThNRXonfRFtVr5ukYhlIEKnaAatSqwMFqREwAevHdauYqEE8fszX5uH7vfW0qD3YRUUdO4lrptsgpLpbQxI_j2URD1VAKkgBHVe7SKXUqRatvHsHHx1iLYKbZd26mpnZraKba9i213o_r68Mp2tSH_IB7qjsD7PfA3NHT734PtyefL6TT62d4PaaDdve_iLyuVUKX9cXlmT79fXeuP6qtdiH-yNZzH</recordid><startdate>200203</startdate><enddate>200203</enddate><creator>Lee, E.-J.</creator><creator>Min, D. S.</creator><creator>Lee, M.-Y.</creator><creator>Chung, J.-W.</creator><creator>Chun, M.-H.</creator><creator>Oh, S.-J.</creator><general>Blackwell Science, Ltd</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>200203</creationdate><title>Differential expression of phospholipase D1 in the developing retina</title><author>Lee, E.-J. ; Min, D. S. ; Lee, M.-Y. ; Chung, J.-W. ; Chun, M.-H. ; Oh, S.-J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5029-da75956374d8e41da6d4cbbdff133790c1a3ef187414987ea300d0dda87ace3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Aging - metabolism</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Lineage - physiology</topic><topic>differentiation</topic><topic>Female</topic><topic>Fetus</topic><topic>Glutamate-Ammonia Ligase - metabolism</topic><topic>Glutamic Acid - metabolism</topic><topic>glutamine synthetase</topic><topic>immunocytochemistry</topic><topic>Immunohistochemistry</topic><topic>Microtubule-Associated Proteins - metabolism</topic><topic>Neuroglia - cytology</topic><topic>Neuroglia - enzymology</topic><topic>Neurons - cytology</topic><topic>Neurons - enzymology</topic><topic>Phospholipase D - metabolism</topic><topic>Pregnancy</topic><topic>rat</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Retina - embryology</topic><topic>Retina - enzymology</topic><topic>Retina - growth & development</topic><topic>Signal Transduction - physiology</topic><topic>Stem Cells - cytology</topic><topic>Stem Cells - enzymology</topic><topic>Western blot analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, E.-J.</creatorcontrib><creatorcontrib>Min, D. S.</creatorcontrib><creatorcontrib>Lee, M.-Y.</creatorcontrib><creatorcontrib>Chung, J.-W.</creatorcontrib><creatorcontrib>Chun, M.-H.</creatorcontrib><creatorcontrib>Oh, S.-J.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The European journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, E.-J.</au><au>Min, D. S.</au><au>Lee, M.-Y.</au><au>Chung, J.-W.</au><au>Chun, M.-H.</au><au>Oh, S.-J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression of phospholipase D1 in the developing retina</atitle><jtitle>The European journal of neuroscience</jtitle><addtitle>Eur J Neurosci</addtitle><date>2002-03</date><risdate>2002</risdate><volume>15</volume><issue>6</issue><spage>1006</spage><epage>1012</epage><pages>1006-1012</pages><issn>0953-816X</issn><eissn>1460-9568</eissn><abstract>Expression patterns of phospholipase D1 (PLD1) in the developing rat retina were investigated using immunocytochemistry and Western blot analysis and compared with the expression patterns of glutamine synthetase. PLD1 immunoreactivity appeared first in a few neuroblasts in the middle of the mantle zone of the primitive retina by embryonic (E) day 13. PLD1‐immunoreactive primitive ganglion cells were characterized in the ganglion cell layer by E17. Faint immunoreactivity at E17 profiled radially orientated cells and this pattern appeared up to postnatal (P) day 7. In the ganglion cell layer at P3, displaced amacrine cells and ganglion cells were classified. At P5, presumptive horizontal cells and amacrine cells were identified. By P7, a thin outermost layer of newly formed segments of the photoreceptor cells was also PLD1 immunoreactive. PLD1 immunoreactivity at P8 was limited to radial Müller cells and the outer segment layer of the photoreceptor cells, and the expression pattern was conserved to adulthood. Western blot analysis showed relatively high amounts of PLD1 protein at E17 and P3, a decrease at P7, and moderate amounts from P8 onward. Co‐expression of PLD1 with glutamine synthetase in the retina appeared first after birth in differentiating neurons and in Müller cells by P8; thereafter the pattern was maintained. The expression pattern of the PLD1 during development of the retina suggests that PLD1 plays important roles in glutamate‐associated differentiation of both specific neurons and radial glial cells, and in glutamate‐mediated cellular signalling in Müller cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science, Ltd</pub><pmid>11918661</pmid><doi>10.1046/j.1460-9568.2002.01939.x</doi><tpages>7</tpages></addata></record> |
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subjects | Aging - metabolism Animals Animals, Newborn Cell Differentiation - physiology Cell Lineage - physiology differentiation Female Fetus Glutamate-Ammonia Ligase - metabolism Glutamic Acid - metabolism glutamine synthetase immunocytochemistry Immunohistochemistry Microtubule-Associated Proteins - metabolism Neuroglia - cytology Neuroglia - enzymology Neurons - cytology Neurons - enzymology Phospholipase D - metabolism Pregnancy rat Rats Rats, Sprague-Dawley Retina - embryology Retina - enzymology Retina - growth & development Signal Transduction - physiology Stem Cells - cytology Stem Cells - enzymology Western blot analysis |
title | Differential expression of phospholipase D1 in the developing retina |
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