Abstract 15628: Endothelial Cell RNAseq in Hypercholesterolemic Zebrafish Reveals Early Dynamic Changes in Neuromast-Enriched Genes
IntroductionThe cellular and molecular phenotypes of atherosclerosis during development are largely unknown. Zebrafish has emerged as an appealing model to understand endothelial dysfunction during early atherogenesis, owing to their translucency enabling real-time imaging and large breeding capacit...
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Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 2019-11, Vol.140 (Suppl_1 Suppl 1), p.A15628-A15628 |
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creator | Dai, Wei Kithcart, Aaron P Rainville, Nicholas Deo, Rahul C Beerens, Manu MacRae, Calum |
description | IntroductionThe cellular and molecular phenotypes of atherosclerosis during development are largely unknown. Zebrafish has emerged as an appealing model to understand endothelial dysfunction during early atherogenesis, owing to their translucency enabling real-time imaging and large breeding capacity for high throughput screening. Furthermore, zebrafish share many of the same developmental pathways as humans, allowing the study of early vascular processes in a fully integrated vertebrate system.MethodsWe fed larval zebrafish regular or high cholesterol diet (4%) for one week from 5 days post fertilization and isolated endothelial enriched compartments by fluorescent activated cell sorting using the endothelial cell marker FLK:GFP. We performed transcriptome profiling of sorted endothelial cells. We also examined endothelial morphological changes in high cholesterol-fed larval fish with live imaging.ResultsIn addition to the anticipated findings in lipid metabolism, we found an unexpected 4-10 fold enrichment of 16 neuromast-related genes in the endothelial-enriched compared to endothelial-depleted cell fractions. The expression of these neuromast-related genes is significantly down-regulated 3.1 +/- 0.5 fold by high cholesterol diet when compared with a control diet. These changes are not observed in unsorted samples or in controls. In association with these defects, there were highly reproducible abnormalities of vascular patterning with significantly increased branching indices estimated using a wide range of endpoints with Image J (p |
doi_str_mv | 10.1161/circ.140.suppl_1.15628 |
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fullrecord | <record><control><sourceid>wolterskluwer</sourceid><recordid>TN_cdi_wolterskluwer_health_00003017-201911191-03254</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>00003017-201911191-03254</sourcerecordid><originalsourceid>FETCH-wolterskluwer_health_00003017-201911191-032543</originalsourceid><addsrcrecordid>eNqdjstOwzAQRS0EEuHxC8g_4OBHHoRdFUK76qJixSZy3Sk2uE6wHaqs-XFcxBewGB2Nrs7MReiO0Zyxit0r41XOCpqHaRxtz3JWVvzhDGWs5AUpStGco4xS2pBacH6JrkJ4T2sl6jJD34ttiF6qiH-tR9y53RA1WCMtbsFavFkvAnxi4_BqHsErPVgIEXzCwSj8Clsv9yZovIEvkDbgTno746fZyVPeauneIJz8NUx-OMgQSee8URp2eAkOwg262CcRbv94jYrn7qVdkeNg06PwYacj-F6n61H3qToVlNWEU9YwloZQwctC_FP7AaIwYbU</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Abstract 15628: Endothelial Cell RNAseq in Hypercholesterolemic Zebrafish Reveals Early Dynamic Changes in Neuromast-Enriched Genes</title><source>American Heart Association Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Journals@Ovid Complete</source><creator>Dai, Wei ; Kithcart, Aaron P ; Rainville, Nicholas ; Deo, Rahul C ; Beerens, Manu ; MacRae, Calum</creator><creatorcontrib>Dai, Wei ; Kithcart, Aaron P ; Rainville, Nicholas ; Deo, Rahul C ; Beerens, Manu ; MacRae, Calum</creatorcontrib><description>IntroductionThe cellular and molecular phenotypes of atherosclerosis during development are largely unknown. Zebrafish has emerged as an appealing model to understand endothelial dysfunction during early atherogenesis, owing to their translucency enabling real-time imaging and large breeding capacity for high throughput screening. Furthermore, zebrafish share many of the same developmental pathways as humans, allowing the study of early vascular processes in a fully integrated vertebrate system.MethodsWe fed larval zebrafish regular or high cholesterol diet (4%) for one week from 5 days post fertilization and isolated endothelial enriched compartments by fluorescent activated cell sorting using the endothelial cell marker FLK:GFP. We performed transcriptome profiling of sorted endothelial cells. We also examined endothelial morphological changes in high cholesterol-fed larval fish with live imaging.ResultsIn addition to the anticipated findings in lipid metabolism, we found an unexpected 4-10 fold enrichment of 16 neuromast-related genes in the endothelial-enriched compared to endothelial-depleted cell fractions. The expression of these neuromast-related genes is significantly down-regulated 3.1 +/- 0.5 fold by high cholesterol diet when compared with a control diet. These changes are not observed in unsorted samples or in controls. In association with these defects, there were highly reproducible abnormalities of vascular patterning with significantly increased branching indices estimated using a wide range of endpoints with Image J (p<0.01).ConclusionsWe have identified a unique pathway abnormality in zebrafish rendered hypercholesterolemic during development that is associated with a series of genes implicated in mechanotransduction. We are currently exploring the mechanistic role of these genes in atherosclerosis biology. These insights into the earliest phases of dyslipidemic vascular biology will inform our understanding of the longitudinal pathogenesis of human disease and also form the basis for high throughput screens to reverse disease mechanisms.</description><identifier>ISSN: 0009-7322</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/circ.140.suppl_1.15628</identifier><language>eng</language><publisher>by the American College of Cardiology Foundation and the American Heart Association, Inc</publisher><ispartof>Circulation (New York, N.Y.), 2019-11, Vol.140 (Suppl_1 Suppl 1), p.A15628-A15628</ispartof><rights>2019 by the American College of Cardiology Foundation and the American Heart Association, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Dai, Wei</creatorcontrib><creatorcontrib>Kithcart, Aaron P</creatorcontrib><creatorcontrib>Rainville, Nicholas</creatorcontrib><creatorcontrib>Deo, Rahul C</creatorcontrib><creatorcontrib>Beerens, Manu</creatorcontrib><creatorcontrib>MacRae, Calum</creatorcontrib><title>Abstract 15628: Endothelial Cell RNAseq in Hypercholesterolemic Zebrafish Reveals Early Dynamic Changes in Neuromast-Enriched Genes</title><title>Circulation (New York, N.Y.)</title><description>IntroductionThe cellular and molecular phenotypes of atherosclerosis during development are largely unknown. Zebrafish has emerged as an appealing model to understand endothelial dysfunction during early atherogenesis, owing to their translucency enabling real-time imaging and large breeding capacity for high throughput screening. Furthermore, zebrafish share many of the same developmental pathways as humans, allowing the study of early vascular processes in a fully integrated vertebrate system.MethodsWe fed larval zebrafish regular or high cholesterol diet (4%) for one week from 5 days post fertilization and isolated endothelial enriched compartments by fluorescent activated cell sorting using the endothelial cell marker FLK:GFP. We performed transcriptome profiling of sorted endothelial cells. We also examined endothelial morphological changes in high cholesterol-fed larval fish with live imaging.ResultsIn addition to the anticipated findings in lipid metabolism, we found an unexpected 4-10 fold enrichment of 16 neuromast-related genes in the endothelial-enriched compared to endothelial-depleted cell fractions. The expression of these neuromast-related genes is significantly down-regulated 3.1 +/- 0.5 fold by high cholesterol diet when compared with a control diet. These changes are not observed in unsorted samples or in controls. In association with these defects, there were highly reproducible abnormalities of vascular patterning with significantly increased branching indices estimated using a wide range of endpoints with Image J (p<0.01).ConclusionsWe have identified a unique pathway abnormality in zebrafish rendered hypercholesterolemic during development that is associated with a series of genes implicated in mechanotransduction. We are currently exploring the mechanistic role of these genes in atherosclerosis biology. These insights into the earliest phases of dyslipidemic vascular biology will inform our understanding of the longitudinal pathogenesis of human disease and also form the basis for high throughput screens to reverse disease mechanisms.</description><issn>0009-7322</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqdjstOwzAQRS0EEuHxC8g_4OBHHoRdFUK76qJixSZy3Sk2uE6wHaqs-XFcxBewGB2Nrs7MReiO0Zyxit0r41XOCpqHaRxtz3JWVvzhDGWs5AUpStGco4xS2pBacH6JrkJ4T2sl6jJD34ttiF6qiH-tR9y53RA1WCMtbsFavFkvAnxi4_BqHsErPVgIEXzCwSj8Clsv9yZovIEvkDbgTno746fZyVPeauneIJz8NUx-OMgQSee8URp2eAkOwg262CcRbv94jYrn7qVdkeNg06PwYacj-F6n61H3qToVlNWEU9YwloZQwctC_FP7AaIwYbU</recordid><startdate>20191119</startdate><enddate>20191119</enddate><creator>Dai, Wei</creator><creator>Kithcart, Aaron P</creator><creator>Rainville, Nicholas</creator><creator>Deo, Rahul C</creator><creator>Beerens, Manu</creator><creator>MacRae, Calum</creator><general>by the American College of Cardiology Foundation and the American Heart Association, Inc</general><scope/></search><sort><creationdate>20191119</creationdate><title>Abstract 15628: Endothelial Cell RNAseq in Hypercholesterolemic Zebrafish Reveals Early Dynamic Changes in Neuromast-Enriched Genes</title><author>Dai, Wei ; Kithcart, Aaron P ; Rainville, Nicholas ; Deo, Rahul C ; Beerens, Manu ; MacRae, Calum</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-wolterskluwer_health_00003017-201911191-032543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Dai, Wei</creatorcontrib><creatorcontrib>Kithcart, Aaron P</creatorcontrib><creatorcontrib>Rainville, Nicholas</creatorcontrib><creatorcontrib>Deo, Rahul C</creatorcontrib><creatorcontrib>Beerens, Manu</creatorcontrib><creatorcontrib>MacRae, Calum</creatorcontrib><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dai, Wei</au><au>Kithcart, Aaron P</au><au>Rainville, Nicholas</au><au>Deo, Rahul C</au><au>Beerens, Manu</au><au>MacRae, Calum</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abstract 15628: Endothelial Cell RNAseq in Hypercholesterolemic Zebrafish Reveals Early Dynamic Changes in Neuromast-Enriched Genes</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><date>2019-11-19</date><risdate>2019</risdate><volume>140</volume><issue>Suppl_1 Suppl 1</issue><spage>A15628</spage><epage>A15628</epage><pages>A15628-A15628</pages><issn>0009-7322</issn><eissn>1524-4539</eissn><abstract>IntroductionThe cellular and molecular phenotypes of atherosclerosis during development are largely unknown. Zebrafish has emerged as an appealing model to understand endothelial dysfunction during early atherogenesis, owing to their translucency enabling real-time imaging and large breeding capacity for high throughput screening. Furthermore, zebrafish share many of the same developmental pathways as humans, allowing the study of early vascular processes in a fully integrated vertebrate system.MethodsWe fed larval zebrafish regular or high cholesterol diet (4%) for one week from 5 days post fertilization and isolated endothelial enriched compartments by fluorescent activated cell sorting using the endothelial cell marker FLK:GFP. We performed transcriptome profiling of sorted endothelial cells. We also examined endothelial morphological changes in high cholesterol-fed larval fish with live imaging.ResultsIn addition to the anticipated findings in lipid metabolism, we found an unexpected 4-10 fold enrichment of 16 neuromast-related genes in the endothelial-enriched compared to endothelial-depleted cell fractions. The expression of these neuromast-related genes is significantly down-regulated 3.1 +/- 0.5 fold by high cholesterol diet when compared with a control diet. These changes are not observed in unsorted samples or in controls. In association with these defects, there were highly reproducible abnormalities of vascular patterning with significantly increased branching indices estimated using a wide range of endpoints with Image J (p<0.01).ConclusionsWe have identified a unique pathway abnormality in zebrafish rendered hypercholesterolemic during development that is associated with a series of genes implicated in mechanotransduction. We are currently exploring the mechanistic role of these genes in atherosclerosis biology. These insights into the earliest phases of dyslipidemic vascular biology will inform our understanding of the longitudinal pathogenesis of human disease and also form the basis for high throughput screens to reverse disease mechanisms.</abstract><pub>by the American College of Cardiology Foundation and the American Heart Association, Inc</pub><doi>10.1161/circ.140.suppl_1.15628</doi></addata></record> |
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source | American Heart Association Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete |
title | Abstract 15628: Endothelial Cell RNAseq in Hypercholesterolemic Zebrafish Reveals Early Dynamic Changes in Neuromast-Enriched Genes |
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