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Functional and developmental analysis of the blood–brain barrier in zebrafish
Abstract The blood–brain barrier (BBB) is essential for maintaining brain homeostasis and protecting the brain from toxic substances. Breakdown of this barrier results in severe brain pathologies, whereas impermeability of the BBB is a major obstacle for drug delivery to the brain. Despite its impor...
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Published in: | Brain research bulletin 2008-03, Vol.75 (5), p.619-628 |
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description | Abstract The blood–brain barrier (BBB) is essential for maintaining brain homeostasis and protecting the brain from toxic substances. Breakdown of this barrier results in severe brain pathologies, whereas impermeability of the BBB is a major obstacle for drug delivery to the brain. Despite its importance, our understanding of the maturation and modulation of the BBB is limited. Zebrafish ( Danio rerio ) has emerged as a useful model organism for studying vertebrate development and disease mechanisms, as well as for preclinical drug screening. However, the nature of the BBB has not yet been examined in teleost fish. In this paper, we report that with the exception of the circumventricular organs, the cerebral microvessels in zebrafish are impermeable to sulfo-NHS-biotin and horseradish peroxidase (HRP). Brain endothelial cells show immunoreactivity to Claudin-5 and Zonula Occludens-1 (ZO-1), implying the presence of tight junctions in these cells. The expression of Claudin-5 and ZO-1 was detected in cerebral microvessels from 3 days post-fertilization (dpf), concomitant with maturation of the BBB, as determined by restricted permeability to HRP and various fluorescent tracers. Real-time analysis of fluorescent tracer leakage in embryonic zebrafish suggests that they may be used as an in vivo model for BBB breakdown. Taken together, our results show that the endothelial tight junction-based BBB of zebrafish is similar to that of higher vertebrates and thus, zebrafish may be an excellent genetic and experimental model organism for studying development and maintenance of the BBB. |
doi_str_mv | 10.1016/j.brainresbull.2007.10.043 |
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Breakdown of this barrier results in severe brain pathologies, whereas impermeability of the BBB is a major obstacle for drug delivery to the brain. Despite its importance, our understanding of the maturation and modulation of the BBB is limited. Zebrafish ( Danio rerio ) has emerged as a useful model organism for studying vertebrate development and disease mechanisms, as well as for preclinical drug screening. However, the nature of the BBB has not yet been examined in teleost fish. In this paper, we report that with the exception of the circumventricular organs, the cerebral microvessels in zebrafish are impermeable to sulfo-NHS-biotin and horseradish peroxidase (HRP). Brain endothelial cells show immunoreactivity to Claudin-5 and Zonula Occludens-1 (ZO-1), implying the presence of tight junctions in these cells. The expression of Claudin-5 and ZO-1 was detected in cerebral microvessels from 3 days post-fertilization (dpf), concomitant with maturation of the BBB, as determined by restricted permeability to HRP and various fluorescent tracers. Real-time analysis of fluorescent tracer leakage in embryonic zebrafish suggests that they may be used as an in vivo model for BBB breakdown. Taken together, our results show that the endothelial tight junction-based BBB of zebrafish is similar to that of higher vertebrates and thus, zebrafish may be an excellent genetic and experimental model organism for studying development and maintenance of the BBB.</description><identifier>ISSN: 0361-9230</identifier><identifier>EISSN: 1873-2747</identifier><identifier>DOI: 10.1016/j.brainresbull.2007.10.043</identifier><identifier>PMID: 18355638</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Animals, Genetically Modified ; Biological Transport - physiology ; Biotin - metabolism ; Blood-Brain Barrier - growth & development ; Blood-Brain Barrier - metabolism ; Capillary Permeability ; Circumventricular organ ; Claudin-5 ; Danio rerio ; Embryo, Nonmammalian ; Endothelial ; Freshwater ; Green Fluorescent Proteins - biosynthesis ; Green Fluorescent Proteins - genetics ; Horseradish Peroxidase - metabolism ; Membrane Proteins ; Neurology ; Proto-Oncogene Protein c-fli-1 - biosynthesis ; Proto-Oncogene Protein c-fli-1 - genetics ; Teleostei ; Tight junction ; Tight Junctions - physiology ; Zebrafish ; ZO-1</subject><ispartof>Brain research bulletin, 2008-03, Vol.75 (5), p.619-628</ispartof><rights>Elsevier Inc.</rights><rights>2007 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-e9d318345182cec56483607c080ce0b80e59db11627523c481e621a3014372f03</citedby><cites>FETCH-LOGICAL-c521t-e9d318345182cec56483607c080ce0b80e59db11627523c481e621a3014372f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18355638$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jeong, Jae-Yeon</creatorcontrib><creatorcontrib>Kwon, Hyouk-Bum</creatorcontrib><creatorcontrib>Ahn, Jong-Chan</creatorcontrib><creatorcontrib>Kang, Dongmin</creatorcontrib><creatorcontrib>Kwon, Seung-Hae</creatorcontrib><creatorcontrib>Park, Jeong Ae</creatorcontrib><creatorcontrib>Kim, Kyu-Won</creatorcontrib><title>Functional and developmental analysis of the blood–brain barrier in zebrafish</title><title>Brain research bulletin</title><addtitle>Brain Res Bull</addtitle><description>Abstract The blood–brain barrier (BBB) is essential for maintaining brain homeostasis and protecting the brain from toxic substances. Breakdown of this barrier results in severe brain pathologies, whereas impermeability of the BBB is a major obstacle for drug delivery to the brain. Despite its importance, our understanding of the maturation and modulation of the BBB is limited. Zebrafish ( Danio rerio ) has emerged as a useful model organism for studying vertebrate development and disease mechanisms, as well as for preclinical drug screening. However, the nature of the BBB has not yet been examined in teleost fish. In this paper, we report that with the exception of the circumventricular organs, the cerebral microvessels in zebrafish are impermeable to sulfo-NHS-biotin and horseradish peroxidase (HRP). Brain endothelial cells show immunoreactivity to Claudin-5 and Zonula Occludens-1 (ZO-1), implying the presence of tight junctions in these cells. The expression of Claudin-5 and ZO-1 was detected in cerebral microvessels from 3 days post-fertilization (dpf), concomitant with maturation of the BBB, as determined by restricted permeability to HRP and various fluorescent tracers. Real-time analysis of fluorescent tracer leakage in embryonic zebrafish suggests that they may be used as an in vivo model for BBB breakdown. Taken together, our results show that the endothelial tight junction-based BBB of zebrafish is similar to that of higher vertebrates and thus, zebrafish may be an excellent genetic and experimental model organism for studying development and maintenance of the BBB.</description><subject>Animals</subject><subject>Animals, Genetically Modified</subject><subject>Biological Transport - physiology</subject><subject>Biotin - metabolism</subject><subject>Blood-Brain Barrier - growth & development</subject><subject>Blood-Brain Barrier - metabolism</subject><subject>Capillary Permeability</subject><subject>Circumventricular organ</subject><subject>Claudin-5</subject><subject>Danio rerio</subject><subject>Embryo, Nonmammalian</subject><subject>Endothelial</subject><subject>Freshwater</subject><subject>Green Fluorescent Proteins - biosynthesis</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Horseradish Peroxidase - metabolism</subject><subject>Membrane Proteins</subject><subject>Neurology</subject><subject>Proto-Oncogene Protein c-fli-1 - biosynthesis</subject><subject>Proto-Oncogene Protein c-fli-1 - genetics</subject><subject>Teleostei</subject><subject>Tight junction</subject><subject>Tight Junctions - physiology</subject><subject>Zebrafish</subject><subject>ZO-1</subject><issn>0361-9230</issn><issn>1873-2747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkcFO3DAQhq2qqGxpX6GKOPSWZWwntsOhUkVLqYTEgfZsOc5EeOuNFztBWk68A2_YJ6nDrkTFiZOtmX_mn_mGkGMKSwpUnKyWbTRuiJjayfslA5A5sYSKvyELqiQvmazkW7IALmjZMA6H5H1KKwAQqhbvyCFVvK4FVwtydT4NdnRhML4wQ1d0eIc-bNY4jE8R47fJpSL0xXiDRetD6P4-PD75F62J0WEs8vcec6h36eYDOeiNT_hx_x6R3-fff51dlJdXP36efb0sbc3oWGLT8TxEVVPFLNpaVIoLkBYUWIRWAdZN11IqmKwZt5WiKBg1HGjFJeuBH5HPu76bGG4nTKNeu2TRezNgmJKmTSWlkjQLT3dCG0NKEXu9iW5t4lZT0DNOvdL_49QzzjmXcebiT3uXqV1j91y655cF33YCzLveZRg6WYeDxc5FtKPugnudz5cXbax3g7PG_8EtplWYYr5E3konpkFfz4ed7woSgDPZ8H9JuaJx</recordid><startdate>20080328</startdate><enddate>20080328</enddate><creator>Jeong, Jae-Yeon</creator><creator>Kwon, Hyouk-Bum</creator><creator>Ahn, Jong-Chan</creator><creator>Kang, Dongmin</creator><creator>Kwon, Seung-Hae</creator><creator>Park, Jeong Ae</creator><creator>Kim, Kyu-Won</creator><general>Elsevier Inc</general><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>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H95</scope><scope>L.G</scope><scope>P64</scope></search><sort><creationdate>20080328</creationdate><title>Functional and developmental analysis of the blood–brain barrier in zebrafish</title><author>Jeong, Jae-Yeon ; Kwon, Hyouk-Bum ; Ahn, Jong-Chan ; Kang, Dongmin ; Kwon, Seung-Hae ; Park, Jeong Ae ; Kim, Kyu-Won</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-e9d318345182cec56483607c080ce0b80e59db11627523c481e621a3014372f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Animals, Genetically Modified</topic><topic>Biological Transport - physiology</topic><topic>Biotin - metabolism</topic><topic>Blood-Brain Barrier - growth & development</topic><topic>Blood-Brain Barrier - metabolism</topic><topic>Capillary Permeability</topic><topic>Circumventricular organ</topic><topic>Claudin-5</topic><topic>Danio rerio</topic><topic>Embryo, Nonmammalian</topic><topic>Endothelial</topic><topic>Freshwater</topic><topic>Green Fluorescent Proteins - biosynthesis</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Horseradish Peroxidase - metabolism</topic><topic>Membrane Proteins</topic><topic>Neurology</topic><topic>Proto-Oncogene Protein c-fli-1 - biosynthesis</topic><topic>Proto-Oncogene Protein c-fli-1 - genetics</topic><topic>Teleostei</topic><topic>Tight junction</topic><topic>Tight Junctions - physiology</topic><topic>Zebrafish</topic><topic>ZO-1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeong, Jae-Yeon</creatorcontrib><creatorcontrib>Kwon, Hyouk-Bum</creatorcontrib><creatorcontrib>Ahn, Jong-Chan</creatorcontrib><creatorcontrib>Kang, Dongmin</creatorcontrib><creatorcontrib>Kwon, Seung-Hae</creatorcontrib><creatorcontrib>Park, Jeong Ae</creatorcontrib><creatorcontrib>Kim, Kyu-Won</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Brain research bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeong, Jae-Yeon</au><au>Kwon, Hyouk-Bum</au><au>Ahn, Jong-Chan</au><au>Kang, Dongmin</au><au>Kwon, Seung-Hae</au><au>Park, Jeong Ae</au><au>Kim, Kyu-Won</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functional and developmental analysis of the blood–brain barrier in zebrafish</atitle><jtitle>Brain research bulletin</jtitle><addtitle>Brain Res Bull</addtitle><date>2008-03-28</date><risdate>2008</risdate><volume>75</volume><issue>5</issue><spage>619</spage><epage>628</epage><pages>619-628</pages><issn>0361-9230</issn><eissn>1873-2747</eissn><abstract>Abstract The blood–brain barrier (BBB) is essential for maintaining brain homeostasis and protecting the brain from toxic substances. Breakdown of this barrier results in severe brain pathologies, whereas impermeability of the BBB is a major obstacle for drug delivery to the brain. Despite its importance, our understanding of the maturation and modulation of the BBB is limited. Zebrafish ( Danio rerio ) has emerged as a useful model organism for studying vertebrate development and disease mechanisms, as well as for preclinical drug screening. However, the nature of the BBB has not yet been examined in teleost fish. In this paper, we report that with the exception of the circumventricular organs, the cerebral microvessels in zebrafish are impermeable to sulfo-NHS-biotin and horseradish peroxidase (HRP). Brain endothelial cells show immunoreactivity to Claudin-5 and Zonula Occludens-1 (ZO-1), implying the presence of tight junctions in these cells. The expression of Claudin-5 and ZO-1 was detected in cerebral microvessels from 3 days post-fertilization (dpf), concomitant with maturation of the BBB, as determined by restricted permeability to HRP and various fluorescent tracers. Real-time analysis of fluorescent tracer leakage in embryonic zebrafish suggests that they may be used as an in vivo model for BBB breakdown. Taken together, our results show that the endothelial tight junction-based BBB of zebrafish is similar to that of higher vertebrates and thus, zebrafish may be an excellent genetic and experimental model organism for studying development and maintenance of the BBB.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18355638</pmid><doi>10.1016/j.brainresbull.2007.10.043</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Animals, Genetically Modified Biological Transport - physiology Biotin - metabolism Blood-Brain Barrier - growth & development Blood-Brain Barrier - metabolism Capillary Permeability Circumventricular organ Claudin-5 Danio rerio Embryo, Nonmammalian Endothelial Freshwater Green Fluorescent Proteins - biosynthesis Green Fluorescent Proteins - genetics Horseradish Peroxidase - metabolism Membrane Proteins Neurology Proto-Oncogene Protein c-fli-1 - biosynthesis Proto-Oncogene Protein c-fli-1 - genetics Teleostei Tight junction Tight Junctions - physiology Zebrafish ZO-1 |
title | Functional and developmental analysis of the blood–brain barrier in zebrafish |
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