Ontogenesis of embryonic porcine ventral mesencephalon in the perspective of its potential use as a xenograft in Parkinson's disease

Human fetal neural dopaminergic tissue can be transplanted and can ameliorate neurological deficiencies in patients with Parkinson's disease (PD). Donor tissue from other species has been used experimentally for several years in animal experiments and is now being considered an attractive alter...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of comparative neurology (1911) 1997-05, Vol.382 (1), p.19-28
Hauptverfasser: Molenaar, G.J., Hogenesch, R.I., Sprengers, M.E.S., Staal, M.J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 28
container_issue 1
container_start_page 19
container_title Journal of comparative neurology (1911)
container_volume 382
creator Molenaar, G.J.
Hogenesch, R.I.
Sprengers, M.E.S.
Staal, M.J.
description Human fetal neural dopaminergic tissue can be transplanted and can ameliorate neurological deficiencies in patients with Parkinson's disease (PD). Donor tissue from other species has been used experimentally for several years in animal experiments and is now being considered an attractive alternative, particularly from a donor species that breeds in large litters, e.g., the pig. We have studied the early ontogenetic development of the mesencephalic dopaminergic system in the pig, utilising an anti‐tyrosine hydroxylase (TH) immunocytochemical technique, and demonstrated the earliest appearance of its cell bodies at embryonic day 20 (E20). We compared the porcine data with those of human fetal development, as revealed by the same technique. Embryonic dopaminergic cell groups resembling the A8, A9, and A10 of the rat are present in the pig and differentiate into the homologous cell groups of human, although interesting quantitative differences are apparent. In the pig, prolonged presence of immature characteristics of TH‐immunoreactive (TH‐i.r.) cell bodies was observed, notwithstanding the early outgrowth of TH‐i.r. axons into the ganglionic eminence. In the human, on the other hand, cell divisions and maturation of dendrites have progressed to a further degree than in the pig, before such distinct outgrowth of axons takes place. In pig embryos of 28 days, cells in the ventral mesencephalon had differentiated into TH containing neurons, which indicates their potential to synthesize dopamine. In spite of their differentiation, these cells still showed immature morphological features (rounded cell bodies with undifferentiated, short processes). Dopamine synthesis by these cells was demonstrated in previous studies by the high performance liquid chromatographic technique (HogenEsch et al. [1993] Can. J. Neurol. Sci. 20(suppl. 4):P.S. 235). In a separate paper, we have described that these porcine 28‐day dopaminergic cells retain their potential for development and outgrowth in culture (van Roon et al. [1995] Res. Neurol. Neurosci. 7:199–205). We conclude that the ventral mesencephalon in pig embryos of 28 days is a potential source of dopaminergic neurons to be used as a xenograft in PD. J. Comp. Neurol. 382:19‐28, 1997. © 1997 Wiley‐Liss Inc.
doi_str_mv 10.1002/(SICI)1096-9861(19970526)382:1<19::AID-CNE2>3.0.CO;2-N
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78999700</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>78999700</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4332-2628e8be297241b10bddfc0e952e8553fce300473fc1bc557979c1a19cd892b03</originalsourceid><addsrcrecordid>eNqFkUtvEzEURkcIVELhJyB5Be1igh-ZhwOqVE1fkUICAsLyyuPcaQ0Tz2BP2mbPD8dDQliA1JV9pfudz_KJohNGh4xS_ubo06SYHDMq01jmKTtiUmY04emxyPmYvWNyPD6dnMXF7JyfiCEdFvO3PJ49igb7yONoEEAsljLNnkbPvP9GKZVS5AfRgWQizakcRD_ntmuu0aI3njQVwVXpNo01mrSN08YiuUXbOVWTFXq0GtsbVTeWGEu6GyQtOt-i7swt9mnT-ZDrQsKExNojUZ4oco-2uXaq6vrYB-W-G-sb-9qTpfGoPD6PnlSq9vhidx5GXy7OPxdX8XR-OSlOp7EeCcFjnvIc8xK5zPiIlYyWy2WlKcqEY54kotIoKB1l4cJKnSSZzKRmikm9zCUvqTiMXm25rWt-rNF3sDJeY10ri83aQ5bL_pcfXmSpyOQoTcLiYruoXeO9wwpaZ1bKbYBR6D0C9B6hlwK9FPjjEYJH6EeA4BF6jyCAQjEHDrMAfrl7wbpc4XKP3Yn7W3xnatz80_pg6X86f88BHG_Bxnd4vwcHaZBmIkvg6-wSzq4-vs-nixQW4hemycm-</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16379465</pqid></control><display><type>article</type><title>Ontogenesis of embryonic porcine ventral mesencephalon in the perspective of its potential use as a xenograft in Parkinson's disease</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Molenaar, G.J. ; Hogenesch, R.I. ; Sprengers, M.E.S. ; Staal, M.J.</creator><creatorcontrib>Molenaar, G.J. ; Hogenesch, R.I. ; Sprengers, M.E.S. ; Staal, M.J.</creatorcontrib><description>Human fetal neural dopaminergic tissue can be transplanted and can ameliorate neurological deficiencies in patients with Parkinson's disease (PD). Donor tissue from other species has been used experimentally for several years in animal experiments and is now being considered an attractive alternative, particularly from a donor species that breeds in large litters, e.g., the pig. We have studied the early ontogenetic development of the mesencephalic dopaminergic system in the pig, utilising an anti‐tyrosine hydroxylase (TH) immunocytochemical technique, and demonstrated the earliest appearance of its cell bodies at embryonic day 20 (E20). We compared the porcine data with those of human fetal development, as revealed by the same technique. Embryonic dopaminergic cell groups resembling the A8, A9, and A10 of the rat are present in the pig and differentiate into the homologous cell groups of human, although interesting quantitative differences are apparent. In the pig, prolonged presence of immature characteristics of TH‐immunoreactive (TH‐i.r.) cell bodies was observed, notwithstanding the early outgrowth of TH‐i.r. axons into the ganglionic eminence. In the human, on the other hand, cell divisions and maturation of dendrites have progressed to a further degree than in the pig, before such distinct outgrowth of axons takes place. In pig embryos of 28 days, cells in the ventral mesencephalon had differentiated into TH containing neurons, which indicates their potential to synthesize dopamine. In spite of their differentiation, these cells still showed immature morphological features (rounded cell bodies with undifferentiated, short processes). Dopamine synthesis by these cells was demonstrated in previous studies by the high performance liquid chromatographic technique (HogenEsch et al. [1993] Can. J. Neurol. Sci. 20(suppl. 4):P.S. 235). In a separate paper, we have described that these porcine 28‐day dopaminergic cells retain their potential for development and outgrowth in culture (van Roon et al. [1995] Res. Neurol. Neurosci. 7:199–205). We conclude that the ventral mesencephalon in pig embryos of 28 days is a potential source of dopaminergic neurons to be used as a xenograft in PD. J. Comp. Neurol. 382:19‐28, 1997. © 1997 Wiley‐Liss Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/(SICI)1096-9861(19970526)382:1&lt;19::AID-CNE2&gt;3.0.CO;2-N</identifier><identifier>PMID: 9136809</identifier><language>eng</language><publisher>New York: John Wiley &amp; Sons, Inc</publisher><subject>Animals ; Brain Tissue Transplantation ; central nervous system ; donor graft ; dopamine ; Embryo, Mammalian ; Embryonic and Fetal Development ; Fetal Tissue Transplantation ; Fetus ; Gestational Age ; Humans ; Hypothalamus - anatomy &amp; histology ; Hypothalamus - embryology ; Mesencephalon - anatomy &amp; histology ; Mesencephalon - embryology ; Mesencephalon - transplantation ; Nerve Fibers - ultrastructure ; Parkinson Disease - surgery ; Rats ; Species Specificity ; substantia nigra ; Swine - embryology ; Tegmentum Mesencephali - anatomy &amp; histology ; Tegmentum Mesencephali - embryology ; Transplantation, Heterologous</subject><ispartof>Journal of comparative neurology (1911), 1997-05, Vol.382 (1), p.19-28</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4332-2628e8be297241b10bddfc0e952e8553fce300473fc1bc557979c1a19cd892b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291096-9861%2819970526%29382%3A1%3C19%3A%3AAID-CNE2%3E3.0.CO%3B2-N$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291096-9861%2819970526%29382%3A1%3C19%3A%3AAID-CNE2%3E3.0.CO%3B2-N$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9136809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Molenaar, G.J.</creatorcontrib><creatorcontrib>Hogenesch, R.I.</creatorcontrib><creatorcontrib>Sprengers, M.E.S.</creatorcontrib><creatorcontrib>Staal, M.J.</creatorcontrib><title>Ontogenesis of embryonic porcine ventral mesencephalon in the perspective of its potential use as a xenograft in Parkinson's disease</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Human fetal neural dopaminergic tissue can be transplanted and can ameliorate neurological deficiencies in patients with Parkinson's disease (PD). Donor tissue from other species has been used experimentally for several years in animal experiments and is now being considered an attractive alternative, particularly from a donor species that breeds in large litters, e.g., the pig. We have studied the early ontogenetic development of the mesencephalic dopaminergic system in the pig, utilising an anti‐tyrosine hydroxylase (TH) immunocytochemical technique, and demonstrated the earliest appearance of its cell bodies at embryonic day 20 (E20). We compared the porcine data with those of human fetal development, as revealed by the same technique. Embryonic dopaminergic cell groups resembling the A8, A9, and A10 of the rat are present in the pig and differentiate into the homologous cell groups of human, although interesting quantitative differences are apparent. In the pig, prolonged presence of immature characteristics of TH‐immunoreactive (TH‐i.r.) cell bodies was observed, notwithstanding the early outgrowth of TH‐i.r. axons into the ganglionic eminence. In the human, on the other hand, cell divisions and maturation of dendrites have progressed to a further degree than in the pig, before such distinct outgrowth of axons takes place. In pig embryos of 28 days, cells in the ventral mesencephalon had differentiated into TH containing neurons, which indicates their potential to synthesize dopamine. In spite of their differentiation, these cells still showed immature morphological features (rounded cell bodies with undifferentiated, short processes). Dopamine synthesis by these cells was demonstrated in previous studies by the high performance liquid chromatographic technique (HogenEsch et al. [1993] Can. J. Neurol. Sci. 20(suppl. 4):P.S. 235). In a separate paper, we have described that these porcine 28‐day dopaminergic cells retain their potential for development and outgrowth in culture (van Roon et al. [1995] Res. Neurol. Neurosci. 7:199–205). We conclude that the ventral mesencephalon in pig embryos of 28 days is a potential source of dopaminergic neurons to be used as a xenograft in PD. J. Comp. Neurol. 382:19‐28, 1997. © 1997 Wiley‐Liss Inc.</description><subject>Animals</subject><subject>Brain Tissue Transplantation</subject><subject>central nervous system</subject><subject>donor graft</subject><subject>dopamine</subject><subject>Embryo, Mammalian</subject><subject>Embryonic and Fetal Development</subject><subject>Fetal Tissue Transplantation</subject><subject>Fetus</subject><subject>Gestational Age</subject><subject>Humans</subject><subject>Hypothalamus - anatomy &amp; histology</subject><subject>Hypothalamus - embryology</subject><subject>Mesencephalon - anatomy &amp; histology</subject><subject>Mesencephalon - embryology</subject><subject>Mesencephalon - transplantation</subject><subject>Nerve Fibers - ultrastructure</subject><subject>Parkinson Disease - surgery</subject><subject>Rats</subject><subject>Species Specificity</subject><subject>substantia nigra</subject><subject>Swine - embryology</subject><subject>Tegmentum Mesencephali - anatomy &amp; histology</subject><subject>Tegmentum Mesencephali - embryology</subject><subject>Transplantation, Heterologous</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtvEzEURkcIVELhJyB5Be1igh-ZhwOqVE1fkUICAsLyyuPcaQ0Tz2BP2mbPD8dDQliA1JV9pfudz_KJohNGh4xS_ubo06SYHDMq01jmKTtiUmY04emxyPmYvWNyPD6dnMXF7JyfiCEdFvO3PJ49igb7yONoEEAsljLNnkbPvP9GKZVS5AfRgWQizakcRD_ntmuu0aI3njQVwVXpNo01mrSN08YiuUXbOVWTFXq0GtsbVTeWGEu6GyQtOt-i7swt9mnT-ZDrQsKExNojUZ4oco-2uXaq6vrYB-W-G-sb-9qTpfGoPD6PnlSq9vhidx5GXy7OPxdX8XR-OSlOp7EeCcFjnvIc8xK5zPiIlYyWy2WlKcqEY54kotIoKB1l4cJKnSSZzKRmikm9zCUvqTiMXm25rWt-rNF3sDJeY10ri83aQ5bL_pcfXmSpyOQoTcLiYruoXeO9wwpaZ1bKbYBR6D0C9B6hlwK9FPjjEYJH6EeA4BF6jyCAQjEHDrMAfrl7wbpc4XKP3Yn7W3xnatz80_pg6X86f88BHG_Bxnd4vwcHaZBmIkvg6-wSzq4-vs-nixQW4hemycm-</recordid><startdate>19970526</startdate><enddate>19970526</enddate><creator>Molenaar, G.J.</creator><creator>Hogenesch, R.I.</creator><creator>Sprengers, M.E.S.</creator><creator>Staal, M.J.</creator><general>John Wiley &amp; Sons, Inc</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>19970526</creationdate><title>Ontogenesis of embryonic porcine ventral mesencephalon in the perspective of its potential use as a xenograft in Parkinson's disease</title><author>Molenaar, G.J. ; Hogenesch, R.I. ; Sprengers, M.E.S. ; Staal, M.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4332-2628e8be297241b10bddfc0e952e8553fce300473fc1bc557979c1a19cd892b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Animals</topic><topic>Brain Tissue Transplantation</topic><topic>central nervous system</topic><topic>donor graft</topic><topic>dopamine</topic><topic>Embryo, Mammalian</topic><topic>Embryonic and Fetal Development</topic><topic>Fetal Tissue Transplantation</topic><topic>Fetus</topic><topic>Gestational Age</topic><topic>Humans</topic><topic>Hypothalamus - anatomy &amp; histology</topic><topic>Hypothalamus - embryology</topic><topic>Mesencephalon - anatomy &amp; histology</topic><topic>Mesencephalon - embryology</topic><topic>Mesencephalon - transplantation</topic><topic>Nerve Fibers - ultrastructure</topic><topic>Parkinson Disease - surgery</topic><topic>Rats</topic><topic>Species Specificity</topic><topic>substantia nigra</topic><topic>Swine - embryology</topic><topic>Tegmentum Mesencephali - anatomy &amp; histology</topic><topic>Tegmentum Mesencephali - embryology</topic><topic>Transplantation, Heterologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Molenaar, G.J.</creatorcontrib><creatorcontrib>Hogenesch, R.I.</creatorcontrib><creatorcontrib>Sprengers, M.E.S.</creatorcontrib><creatorcontrib>Staal, M.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>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Molenaar, G.J.</au><au>Hogenesch, R.I.</au><au>Sprengers, M.E.S.</au><au>Staal, M.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ontogenesis of embryonic porcine ventral mesencephalon in the perspective of its potential use as a xenograft in Parkinson's disease</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>1997-05-26</date><risdate>1997</risdate><volume>382</volume><issue>1</issue><spage>19</spage><epage>28</epage><pages>19-28</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Human fetal neural dopaminergic tissue can be transplanted and can ameliorate neurological deficiencies in patients with Parkinson's disease (PD). Donor tissue from other species has been used experimentally for several years in animal experiments and is now being considered an attractive alternative, particularly from a donor species that breeds in large litters, e.g., the pig. We have studied the early ontogenetic development of the mesencephalic dopaminergic system in the pig, utilising an anti‐tyrosine hydroxylase (TH) immunocytochemical technique, and demonstrated the earliest appearance of its cell bodies at embryonic day 20 (E20). We compared the porcine data with those of human fetal development, as revealed by the same technique. Embryonic dopaminergic cell groups resembling the A8, A9, and A10 of the rat are present in the pig and differentiate into the homologous cell groups of human, although interesting quantitative differences are apparent. In the pig, prolonged presence of immature characteristics of TH‐immunoreactive (TH‐i.r.) cell bodies was observed, notwithstanding the early outgrowth of TH‐i.r. axons into the ganglionic eminence. In the human, on the other hand, cell divisions and maturation of dendrites have progressed to a further degree than in the pig, before such distinct outgrowth of axons takes place. In pig embryos of 28 days, cells in the ventral mesencephalon had differentiated into TH containing neurons, which indicates their potential to synthesize dopamine. In spite of their differentiation, these cells still showed immature morphological features (rounded cell bodies with undifferentiated, short processes). Dopamine synthesis by these cells was demonstrated in previous studies by the high performance liquid chromatographic technique (HogenEsch et al. [1993] Can. J. Neurol. Sci. 20(suppl. 4):P.S. 235). In a separate paper, we have described that these porcine 28‐day dopaminergic cells retain their potential for development and outgrowth in culture (van Roon et al. [1995] Res. Neurol. Neurosci. 7:199–205). We conclude that the ventral mesencephalon in pig embryos of 28 days is a potential source of dopaminergic neurons to be used as a xenograft in PD. J. Comp. Neurol. 382:19‐28, 1997. © 1997 Wiley‐Liss Inc.</abstract><cop>New York</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>9136809</pmid><doi>10.1002/(SICI)1096-9861(19970526)382:1&lt;19::AID-CNE2&gt;3.0.CO;2-N</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-9967
ispartof Journal of comparative neurology (1911), 1997-05, Vol.382 (1), p.19-28
issn 0021-9967
1096-9861
language eng
recordid cdi_proquest_miscellaneous_78999700
source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Animals
Brain Tissue Transplantation
central nervous system
donor graft
dopamine
Embryo, Mammalian
Embryonic and Fetal Development
Fetal Tissue Transplantation
Fetus
Gestational Age
Humans
Hypothalamus - anatomy & histology
Hypothalamus - embryology
Mesencephalon - anatomy & histology
Mesencephalon - embryology
Mesencephalon - transplantation
Nerve Fibers - ultrastructure
Parkinson Disease - surgery
Rats
Species Specificity
substantia nigra
Swine - embryology
Tegmentum Mesencephali - anatomy & histology
Tegmentum Mesencephali - embryology
Transplantation, Heterologous
title Ontogenesis of embryonic porcine ventral mesencephalon in the perspective of its potential use as a xenograft in Parkinson's disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T00%3A01%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ontogenesis%20of%20embryonic%20porcine%20ventral%20mesencephalon%20in%20the%20perspective%20of%20its%20potential%20use%20as%20a%20xenograft%20in%20Parkinson's%20disease&rft.jtitle=Journal%20of%20comparative%20neurology%20(1911)&rft.au=Molenaar,%20G.J.&rft.date=1997-05-26&rft.volume=382&rft.issue=1&rft.spage=19&rft.epage=28&rft.pages=19-28&rft.issn=0021-9967&rft.eissn=1096-9861&rft_id=info:doi/10.1002/(SICI)1096-9861(19970526)382:1%3C19::AID-CNE2%3E3.0.CO;2-N&rft_dat=%3Cproquest_cross%3E78999700%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16379465&rft_id=info:pmid/9136809&rfr_iscdi=true