Target-dependent differentiation and development of molluscan neurons and neuroendocrine cells: use of parasitisation as a tool
Specimens of the freshwater snail Lymnaea stagnalis infected with the schistosome parasite Trichobilharzia ocellata show a strongly inhibited development of their reproductive tract. We hypothesised that the effects of the underdevelopment of targets are reflected at the level of the neuronal develo...
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description | Specimens of the freshwater snail
Lymnaea stagnalis infected with the schistosome parasite
Trichobilharzia ocellata show a strongly inhibited development of their reproductive tract. We hypothesised that the effects of the underdevelopment of targets are reflected at the level of the neuronal development of (i) the motor neurons innervating the male copulation organ and (ii) neuroendocrine cells regulating the gonad. We determined the state of neuronal development by measuring cell number, cell size and neuropeptide gene expression. Our results show that the neuronal development of both copulation controlling anterior lobe motor neurons of the right cerebral ganglion and neuroendocrine caudodorsal cells, which produce neuropeptides regulating ovulation, egg laying and accompanying behaviour, are affected in parasitised animals in which their respective target organs were not developed. The cell bodies were smaller and fewer cells were found to express neuropeptide genes compared to those in non-parasitised animals. These effects were not observed in the appropriate controls. Backfills and lesions of the penis nerve have shown that the inhibited development of central motor neurons in parasitised snails is target dependent; neighbouring neurons that have no connection with the male copulation organ are not affected. Our data suggest that this effect is established by target-derived neurotrophic factors that need this connection for being transported to the innervating motor neurons. We propose that the effect on the neuroendocrine caudodorsal cells is mediated by a humoral factor, since they have no known connection with their target.
We have shown that the size and gene expression of motor neurons controlling copulation behaviour in the pond snail
Lymnaea stagnalis are related to the size of their target, the copulation organ, and depend on the connection with this target. |
doi_str_mv | 10.1016/S0306-4522(00)00556-X |
format | Article |
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Lymnaea stagnalis infected with the schistosome parasite
Trichobilharzia ocellata show a strongly inhibited development of their reproductive tract. We hypothesised that the effects of the underdevelopment of targets are reflected at the level of the neuronal development of (i) the motor neurons innervating the male copulation organ and (ii) neuroendocrine cells regulating the gonad. We determined the state of neuronal development by measuring cell number, cell size and neuropeptide gene expression. Our results show that the neuronal development of both copulation controlling anterior lobe motor neurons of the right cerebral ganglion and neuroendocrine caudodorsal cells, which produce neuropeptides regulating ovulation, egg laying and accompanying behaviour, are affected in parasitised animals in which their respective target organs were not developed. The cell bodies were smaller and fewer cells were found to express neuropeptide genes compared to those in non-parasitised animals. These effects were not observed in the appropriate controls. Backfills and lesions of the penis nerve have shown that the inhibited development of central motor neurons in parasitised snails is target dependent; neighbouring neurons that have no connection with the male copulation organ are not affected. Our data suggest that this effect is established by target-derived neurotrophic factors that need this connection for being transported to the innervating motor neurons. We propose that the effect on the neuroendocrine caudodorsal cells is mediated by a humoral factor, since they have no known connection with their target.
We have shown that the size and gene expression of motor neurons controlling copulation behaviour in the pond snail
Lymnaea stagnalis are related to the size of their target, the copulation organ, and depend on the connection with this target.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/S0306-4522(00)00556-X</identifier><identifier>PMID: 11311809</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Biological and medical sciences ; Cell Count ; Cell Differentiation ; Cell Size ; Female ; Fundamental and applied biological sciences. Psychology ; Gonads - innervation ; Immunohistochemistry ; Invertebrates ; Life cycle. Embryology. Development ; Lymnaea stagnalis ; Male ; Mollusca ; Mollusca - parasitology ; motor neurons ; Motor Neurons - cytology ; Motor Neurons - metabolism ; neuroendocrine cells ; Neuropeptide Y - metabolism ; Neuropeptides - metabolism ; Neurosecretory Systems - cytology ; Physiology. Development ; polyploidy ; Schistosoma ; schistosome parasites ; snail brain ; target organs ; Trichobilharzia ocellata</subject><ispartof>Neuroscience, 2001-01, Vol.103 (1), p.289-299</ispartof><rights>2001 IBRO</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-1d1bda69b04eadc0f2f1f52629ff788bc626d72e647070a18fd445145e458e0e3</citedby><cites>FETCH-LOGICAL-c420t-1d1bda69b04eadc0f2f1f52629ff788bc626d72e647070a18fd445145e458e0e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0306-4522(00)00556-X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=906421$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11311809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Lange, R.P.J</creatorcontrib><creatorcontrib>Moorer-van Delft, C.M</creatorcontrib><creatorcontrib>de Boer, P.A.C.M</creatorcontrib><creatorcontrib>van Minnen, J</creatorcontrib><creatorcontrib>de Jong-Brink, M</creatorcontrib><title>Target-dependent differentiation and development of molluscan neurons and neuroendocrine cells: use of parasitisation as a tool</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Specimens of the freshwater snail
Lymnaea stagnalis infected with the schistosome parasite
Trichobilharzia ocellata show a strongly inhibited development of their reproductive tract. We hypothesised that the effects of the underdevelopment of targets are reflected at the level of the neuronal development of (i) the motor neurons innervating the male copulation organ and (ii) neuroendocrine cells regulating the gonad. We determined the state of neuronal development by measuring cell number, cell size and neuropeptide gene expression. Our results show that the neuronal development of both copulation controlling anterior lobe motor neurons of the right cerebral ganglion and neuroendocrine caudodorsal cells, which produce neuropeptides regulating ovulation, egg laying and accompanying behaviour, are affected in parasitised animals in which their respective target organs were not developed. The cell bodies were smaller and fewer cells were found to express neuropeptide genes compared to those in non-parasitised animals. These effects were not observed in the appropriate controls. Backfills and lesions of the penis nerve have shown that the inhibited development of central motor neurons in parasitised snails is target dependent; neighbouring neurons that have no connection with the male copulation organ are not affected. Our data suggest that this effect is established by target-derived neurotrophic factors that need this connection for being transported to the innervating motor neurons. We propose that the effect on the neuroendocrine caudodorsal cells is mediated by a humoral factor, since they have no known connection with their target.
We have shown that the size and gene expression of motor neurons controlling copulation behaviour in the pond snail
Lymnaea stagnalis are related to the size of their target, the copulation organ, and depend on the connection with this target.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Count</subject><subject>Cell Differentiation</subject><subject>Cell Size</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gonads - innervation</subject><subject>Immunohistochemistry</subject><subject>Invertebrates</subject><subject>Life cycle. Embryology. Development</subject><subject>Lymnaea stagnalis</subject><subject>Male</subject><subject>Mollusca</subject><subject>Mollusca - parasitology</subject><subject>motor neurons</subject><subject>Motor Neurons - cytology</subject><subject>Motor Neurons - metabolism</subject><subject>neuroendocrine cells</subject><subject>Neuropeptide Y - metabolism</subject><subject>Neuropeptides - metabolism</subject><subject>Neurosecretory Systems - cytology</subject><subject>Physiology. Development</subject><subject>polyploidy</subject><subject>Schistosoma</subject><subject>schistosome parasites</subject><subject>snail brain</subject><subject>target organs</subject><subject>Trichobilharzia ocellata</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUFrFTEUhYNY7LP6E5QBQXQxepNJMjPdiBS1hYILK3QX8pIbicwkYzJTcNW_bua9oS6bTS7kOyeXcwh5ReEDBSo__oAGZM0FY-8A3gMIIevbJ2RHu7apW8H5U7J7QE7J85x_QzmCN8_IKaUNpR30O3J_o9MvnGuLEwaLYa6sdw5TmbyefQyVDrayeIdDnMb1PbpqjMOwZKNDFXBJMeQDdJiLSTTJB6wMDkM-r5aMq2TSSWc_-7yZFkk1xzi8ICdODxlfbvcZ-fn1y83FZX39_dvVxefr2nAGc00t3Vst-z1w1NaAY446wSTrnWu7bm8kk7ZlKHkLLWjaOcu5oFwgFx0CNmfk7dF3SvHPgnlWo8_rijpgXLJqi47yRjwK0o7Kpu36AoojaFLMOaFTU_KjTn8VBbVWpA4VqTV_BaAOFanbonu9fbDsR7T_VVsnBXizAbpkPLikg_H5getBckYL9elIYUntzmNS2XgMBq1PaGZlo39kkX-nH6-e</recordid><startdate>20010101</startdate><enddate>20010101</enddate><creator>de Lange, R.P.J</creator><creator>Moorer-van Delft, C.M</creator><creator>de Boer, P.A.C.M</creator><creator>van Minnen, J</creator><creator>de Jong-Brink, M</creator><general>Elsevier Ltd</general><general>Elsevier</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>F1W</scope><scope>H95</scope><scope>L.G</scope><scope>7X8</scope></search><sort><creationdate>20010101</creationdate><title>Target-dependent differentiation and development of molluscan neurons and neuroendocrine cells: use of parasitisation as a tool</title><author>de Lange, R.P.J ; Moorer-van Delft, C.M ; de Boer, P.A.C.M ; van Minnen, J ; de Jong-Brink, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-1d1bda69b04eadc0f2f1f52629ff788bc626d72e647070a18fd445145e458e0e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Count</topic><topic>Cell Differentiation</topic><topic>Cell Size</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gonads - innervation</topic><topic>Immunohistochemistry</topic><topic>Invertebrates</topic><topic>Life cycle. Embryology. Development</topic><topic>Lymnaea stagnalis</topic><topic>Male</topic><topic>Mollusca</topic><topic>Mollusca - parasitology</topic><topic>motor neurons</topic><topic>Motor Neurons - cytology</topic><topic>Motor Neurons - metabolism</topic><topic>neuroendocrine cells</topic><topic>Neuropeptide Y - metabolism</topic><topic>Neuropeptides - metabolism</topic><topic>Neurosecretory Systems - cytology</topic><topic>Physiology. Development</topic><topic>polyploidy</topic><topic>Schistosoma</topic><topic>schistosome parasites</topic><topic>snail brain</topic><topic>target organs</topic><topic>Trichobilharzia ocellata</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Lange, R.P.J</creatorcontrib><creatorcontrib>Moorer-van Delft, C.M</creatorcontrib><creatorcontrib>de Boer, P.A.C.M</creatorcontrib><creatorcontrib>van Minnen, J</creatorcontrib><creatorcontrib>de Jong-Brink, M</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>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>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Lange, R.P.J</au><au>Moorer-van Delft, C.M</au><au>de Boer, P.A.C.M</au><au>van Minnen, J</au><au>de Jong-Brink, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Target-dependent differentiation and development of molluscan neurons and neuroendocrine cells: use of parasitisation as a tool</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2001-01-01</date><risdate>2001</risdate><volume>103</volume><issue>1</issue><spage>289</spage><epage>299</epage><pages>289-299</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Specimens of the freshwater snail
Lymnaea stagnalis infected with the schistosome parasite
Trichobilharzia ocellata show a strongly inhibited development of their reproductive tract. We hypothesised that the effects of the underdevelopment of targets are reflected at the level of the neuronal development of (i) the motor neurons innervating the male copulation organ and (ii) neuroendocrine cells regulating the gonad. We determined the state of neuronal development by measuring cell number, cell size and neuropeptide gene expression. Our results show that the neuronal development of both copulation controlling anterior lobe motor neurons of the right cerebral ganglion and neuroendocrine caudodorsal cells, which produce neuropeptides regulating ovulation, egg laying and accompanying behaviour, are affected in parasitised animals in which their respective target organs were not developed. The cell bodies were smaller and fewer cells were found to express neuropeptide genes compared to those in non-parasitised animals. These effects were not observed in the appropriate controls. Backfills and lesions of the penis nerve have shown that the inhibited development of central motor neurons in parasitised snails is target dependent; neighbouring neurons that have no connection with the male copulation organ are not affected. Our data suggest that this effect is established by target-derived neurotrophic factors that need this connection for being transported to the innervating motor neurons. We propose that the effect on the neuroendocrine caudodorsal cells is mediated by a humoral factor, since they have no known connection with their target.
We have shown that the size and gene expression of motor neurons controlling copulation behaviour in the pond snail
Lymnaea stagnalis are related to the size of their target, the copulation organ, and depend on the connection with this target.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>11311809</pmid><doi>10.1016/S0306-4522(00)00556-X</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cell Count Cell Differentiation Cell Size Female Fundamental and applied biological sciences. Psychology Gonads - innervation Immunohistochemistry Invertebrates Life cycle. Embryology. Development Lymnaea stagnalis Male Mollusca Mollusca - parasitology motor neurons Motor Neurons - cytology Motor Neurons - metabolism neuroendocrine cells Neuropeptide Y - metabolism Neuropeptides - metabolism Neurosecretory Systems - cytology Physiology. Development polyploidy Schistosoma schistosome parasites snail brain target organs Trichobilharzia ocellata |
title | Target-dependent differentiation and development of molluscan neurons and neuroendocrine cells: use of parasitisation as a tool |
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