A histological survey of green fluorescent protein expression in ‘green’ mice: implications for stem cell research
The transgenic enhanced green fluorescent protein (EGFP) expressing ‘green’ mouse (C57BL/6-TgN(ACTbEGFP)IOsb) is a widely used tool in stem cell research, where the ubiquitous nature of EGFP expression is critical to track the fate of single or small groups of transplanted haematopoietic stem cells...
Gespeichert in:
Veröffentlicht in: | Pathology 2007-04, Vol.39 (2), p.247-251 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 251 |
---|---|
container_issue | 2 |
container_start_page | 247 |
container_title | Pathology |
container_volume | 39 |
creator | Biankin, Sandra A. Collector, Michael I. Biankin, Andrew V. Brown, Lindsey J. Kleeberger, Wolfram Devereux, Wendy L. Zahnow, Cynthia A. Baylin, Stephen B. Neil Watkins, D. Sharkis, Saul J. Leach, Steven D. |
description | The transgenic enhanced green fluorescent protein (EGFP) expressing ‘green’ mouse (C57BL/6-TgN(ACTbEGFP)IOsb) is a widely used tool in stem cell research, where the ubiquitous nature of EGFP expression is critical to track the fate of single or small groups of transplanted haematopoietic stem cells (HSC). Our aim was to investigate this assumed ubiquitous expression by performing a detailed histological survey of EGFP expression in these mice.
Fluorescent microscopy of frozen tissue sections was used to perform a detailed histological survey of the pattern of EGFP expression in these mice. Flow cytometry was also used to determine the expression pattern in blood and bone marrow.
Three patterns of EGFP expression were noted. In most tissues there was an apparently stochastic variegation of the transgene, with individual cell types demonstrating highly variable rates of EGFP expression. Certain specific cell types such as pancreatic ductal epithelium, cerebral cortical neurones and glial cells and glomerular mesangial cells consistently lacked EGFP expression, while others, including pancreatic islet cells, expressed EGFP only at extremely low levels, barely distinguishable from background. Lastly, in the colon and stomach the pattern of EGFP expression was suggestive of clonal inactivation. Only cardiac and skeletal muscle showed near ubiquitous expression.
These findings raise questions regarding the ‘ubiquitous’ expression of EGFP in these transgenic mice and suggest caution in relying overly on EGFP alone as an infallible marker of donor cell origin. |
doi_str_mv | 10.1080/00313020701230807 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70415924</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S003130251633803X</els_id><sourcerecordid>20768834</sourcerecordid><originalsourceid>FETCH-LOGICAL-c434t-8d3a1fa236d94c7f6a102f17ee2b0042d5e7f5b265805050b0effe6df51b9cff3</originalsourceid><addsrcrecordid>eNqFkc1OxCAUhYnR6Dj6AG4MK3dVKNB2dGWMf4mJG10TSi8zmLaMQCe68zH09XwSGWcSFyYaFoTLd07uPRehA0qOKanICSGMMpKTktCcpUK5gUaUFyJjE0Y30Wj5nyVA7KDdEJ4IIbyqqm20Q0sueCmKEVqc45kN0bVuarVqcRj8Al6xM3jqAXps2sF5CBr6iOfeRbA9hpd5KgXrepxen2_v3-jn2wfurIZTbLt5m8xiAgI2zuMQocMa2hYnHSivZ3toy6g2wP76HqPHq8uHi5vs7v769uL8LtOc8ZhVDVPUqJwVzYTr0hSKktzQEiCv0zB5I6A0os4LURGRTk3AGCgaI2g90cawMTpa-abenwcIUXY2LDtRPbghyJJwKiY5_xdMIRdVxZYgXYHauxA8GDn3tlP-VVIil1uRv7aSNIdr86HuoPlRrNeQgLMVYPuUV6dmoNo408qDfHKD71NEf9qv1ZCSXFjwMmgLvYbGetBRNs7-of4Clpev5w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20768834</pqid></control><display><type>article</type><title>A histological survey of green fluorescent protein expression in ‘green’ mice: implications for stem cell research</title><source>MEDLINE</source><source>Taylor & Francis Journals Complete</source><source>Alma/SFX Local Collection</source><creator>Biankin, Sandra A. ; Collector, Michael I. ; Biankin, Andrew V. ; Brown, Lindsey J. ; Kleeberger, Wolfram ; Devereux, Wendy L. ; Zahnow, Cynthia A. ; Baylin, Stephen B. ; Neil Watkins, D. ; Sharkis, Saul J. ; Leach, Steven D.</creator><creatorcontrib>Biankin, Sandra A. ; Collector, Michael I. ; Biankin, Andrew V. ; Brown, Lindsey J. ; Kleeberger, Wolfram ; Devereux, Wendy L. ; Zahnow, Cynthia A. ; Baylin, Stephen B. ; Neil Watkins, D. ; Sharkis, Saul J. ; Leach, Steven D.</creatorcontrib><description>The transgenic enhanced green fluorescent protein (EGFP) expressing ‘green’ mouse (C57BL/6-TgN(ACTbEGFP)IOsb) is a widely used tool in stem cell research, where the ubiquitous nature of EGFP expression is critical to track the fate of single or small groups of transplanted haematopoietic stem cells (HSC). Our aim was to investigate this assumed ubiquitous expression by performing a detailed histological survey of EGFP expression in these mice.
Fluorescent microscopy of frozen tissue sections was used to perform a detailed histological survey of the pattern of EGFP expression in these mice. Flow cytometry was also used to determine the expression pattern in blood and bone marrow.
Three patterns of EGFP expression were noted. In most tissues there was an apparently stochastic variegation of the transgene, with individual cell types demonstrating highly variable rates of EGFP expression. Certain specific cell types such as pancreatic ductal epithelium, cerebral cortical neurones and glial cells and glomerular mesangial cells consistently lacked EGFP expression, while others, including pancreatic islet cells, expressed EGFP only at extremely low levels, barely distinguishable from background. Lastly, in the colon and stomach the pattern of EGFP expression was suggestive of clonal inactivation. Only cardiac and skeletal muscle showed near ubiquitous expression.
These findings raise questions regarding the ‘ubiquitous’ expression of EGFP in these transgenic mice and suggest caution in relying overly on EGFP alone as an infallible marker of donor cell origin.</description><identifier>ISSN: 0031-3025</identifier><identifier>EISSN: 1465-3931</identifier><identifier>DOI: 10.1080/00313020701230807</identifier><identifier>PMID: 17454756</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Animals ; Biomedical Research - methods ; Cell Lineage ; Flow Cytometry ; Fluorescent Antibody Technique ; GFP expression ; GFP Mice ; Green Fluorescent Proteins - biosynthesis ; Green Fluorescent Proteins - genetics ; Mice ; Mice, Transgenic ; Microscopy, Fluorescence ; Models, Animal ; stem cell transplantation ; Stem Cells</subject><ispartof>Pathology, 2007-04, Vol.39 (2), p.247-251</ispartof><rights>2007 Royal College of Pathologists of Australasia</rights><rights>2007 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-8d3a1fa236d94c7f6a102f17ee2b0042d5e7f5b265805050b0effe6df51b9cff3</citedby><cites>FETCH-LOGICAL-c434t-8d3a1fa236d94c7f6a102f17ee2b0042d5e7f5b265805050b0effe6df51b9cff3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00313020701230807$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00313020701230807$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,61194,61375</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17454756$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Biankin, Sandra A.</creatorcontrib><creatorcontrib>Collector, Michael I.</creatorcontrib><creatorcontrib>Biankin, Andrew V.</creatorcontrib><creatorcontrib>Brown, Lindsey J.</creatorcontrib><creatorcontrib>Kleeberger, Wolfram</creatorcontrib><creatorcontrib>Devereux, Wendy L.</creatorcontrib><creatorcontrib>Zahnow, Cynthia A.</creatorcontrib><creatorcontrib>Baylin, Stephen B.</creatorcontrib><creatorcontrib>Neil Watkins, D.</creatorcontrib><creatorcontrib>Sharkis, Saul J.</creatorcontrib><creatorcontrib>Leach, Steven D.</creatorcontrib><title>A histological survey of green fluorescent protein expression in ‘green’ mice: implications for stem cell research</title><title>Pathology</title><addtitle>Pathology</addtitle><description>The transgenic enhanced green fluorescent protein (EGFP) expressing ‘green’ mouse (C57BL/6-TgN(ACTbEGFP)IOsb) is a widely used tool in stem cell research, where the ubiquitous nature of EGFP expression is critical to track the fate of single or small groups of transplanted haematopoietic stem cells (HSC). Our aim was to investigate this assumed ubiquitous expression by performing a detailed histological survey of EGFP expression in these mice.
Fluorescent microscopy of frozen tissue sections was used to perform a detailed histological survey of the pattern of EGFP expression in these mice. Flow cytometry was also used to determine the expression pattern in blood and bone marrow.
Three patterns of EGFP expression were noted. In most tissues there was an apparently stochastic variegation of the transgene, with individual cell types demonstrating highly variable rates of EGFP expression. Certain specific cell types such as pancreatic ductal epithelium, cerebral cortical neurones and glial cells and glomerular mesangial cells consistently lacked EGFP expression, while others, including pancreatic islet cells, expressed EGFP only at extremely low levels, barely distinguishable from background. Lastly, in the colon and stomach the pattern of EGFP expression was suggestive of clonal inactivation. Only cardiac and skeletal muscle showed near ubiquitous expression.
These findings raise questions regarding the ‘ubiquitous’ expression of EGFP in these transgenic mice and suggest caution in relying overly on EGFP alone as an infallible marker of donor cell origin.</description><subject>Animals</subject><subject>Biomedical Research - methods</subject><subject>Cell Lineage</subject><subject>Flow Cytometry</subject><subject>Fluorescent Antibody Technique</subject><subject>GFP expression</subject><subject>GFP Mice</subject><subject>Green Fluorescent Proteins - biosynthesis</subject><subject>Green Fluorescent Proteins - genetics</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Microscopy, Fluorescence</subject><subject>Models, Animal</subject><subject>stem cell transplantation</subject><subject>Stem Cells</subject><issn>0031-3025</issn><issn>1465-3931</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1OxCAUhYnR6Dj6AG4MK3dVKNB2dGWMf4mJG10TSi8zmLaMQCe68zH09XwSGWcSFyYaFoTLd07uPRehA0qOKanICSGMMpKTktCcpUK5gUaUFyJjE0Y30Wj5nyVA7KDdEJ4IIbyqqm20Q0sueCmKEVqc45kN0bVuarVqcRj8Al6xM3jqAXps2sF5CBr6iOfeRbA9hpd5KgXrepxen2_v3-jn2wfurIZTbLt5m8xiAgI2zuMQocMa2hYnHSivZ3toy6g2wP76HqPHq8uHi5vs7v769uL8LtOc8ZhVDVPUqJwVzYTr0hSKktzQEiCv0zB5I6A0os4LURGRTk3AGCgaI2g90cawMTpa-abenwcIUXY2LDtRPbghyJJwKiY5_xdMIRdVxZYgXYHauxA8GDn3tlP-VVIil1uRv7aSNIdr86HuoPlRrNeQgLMVYPuUV6dmoNo408qDfHKD71NEf9qv1ZCSXFjwMmgLvYbGetBRNs7-of4Clpev5w</recordid><startdate>20070401</startdate><enddate>20070401</enddate><creator>Biankin, Sandra A.</creator><creator>Collector, Michael I.</creator><creator>Biankin, Andrew V.</creator><creator>Brown, Lindsey J.</creator><creator>Kleeberger, Wolfram</creator><creator>Devereux, Wendy L.</creator><creator>Zahnow, Cynthia A.</creator><creator>Baylin, Stephen B.</creator><creator>Neil Watkins, D.</creator><creator>Sharkis, Saul J.</creator><creator>Leach, Steven D.</creator><general>Elsevier B.V</general><general>Informa UK Ltd</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20070401</creationdate><title>A histological survey of green fluorescent protein expression in ‘green’ mice: implications for stem cell research</title><author>Biankin, Sandra A. ; Collector, Michael I. ; Biankin, Andrew V. ; Brown, Lindsey J. ; Kleeberger, Wolfram ; Devereux, Wendy L. ; Zahnow, Cynthia A. ; Baylin, Stephen B. ; Neil Watkins, D. ; Sharkis, Saul J. ; Leach, Steven D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-8d3a1fa236d94c7f6a102f17ee2b0042d5e7f5b265805050b0effe6df51b9cff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Biomedical Research - methods</topic><topic>Cell Lineage</topic><topic>Flow Cytometry</topic><topic>Fluorescent Antibody Technique</topic><topic>GFP expression</topic><topic>GFP Mice</topic><topic>Green Fluorescent Proteins - biosynthesis</topic><topic>Green Fluorescent Proteins - genetics</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Microscopy, Fluorescence</topic><topic>Models, Animal</topic><topic>stem cell transplantation</topic><topic>Stem Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Biankin, Sandra A.</creatorcontrib><creatorcontrib>Collector, Michael I.</creatorcontrib><creatorcontrib>Biankin, Andrew V.</creatorcontrib><creatorcontrib>Brown, Lindsey J.</creatorcontrib><creatorcontrib>Kleeberger, Wolfram</creatorcontrib><creatorcontrib>Devereux, Wendy L.</creatorcontrib><creatorcontrib>Zahnow, Cynthia A.</creatorcontrib><creatorcontrib>Baylin, Stephen B.</creatorcontrib><creatorcontrib>Neil Watkins, D.</creatorcontrib><creatorcontrib>Sharkis, Saul J.</creatorcontrib><creatorcontrib>Leach, Steven D.</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Biankin, Sandra A.</au><au>Collector, Michael I.</au><au>Biankin, Andrew V.</au><au>Brown, Lindsey J.</au><au>Kleeberger, Wolfram</au><au>Devereux, Wendy L.</au><au>Zahnow, Cynthia A.</au><au>Baylin, Stephen B.</au><au>Neil Watkins, D.</au><au>Sharkis, Saul J.</au><au>Leach, Steven D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A histological survey of green fluorescent protein expression in ‘green’ mice: implications for stem cell research</atitle><jtitle>Pathology</jtitle><addtitle>Pathology</addtitle><date>2007-04-01</date><risdate>2007</risdate><volume>39</volume><issue>2</issue><spage>247</spage><epage>251</epage><pages>247-251</pages><issn>0031-3025</issn><eissn>1465-3931</eissn><abstract>The transgenic enhanced green fluorescent protein (EGFP) expressing ‘green’ mouse (C57BL/6-TgN(ACTbEGFP)IOsb) is a widely used tool in stem cell research, where the ubiquitous nature of EGFP expression is critical to track the fate of single or small groups of transplanted haematopoietic stem cells (HSC). Our aim was to investigate this assumed ubiquitous expression by performing a detailed histological survey of EGFP expression in these mice.
Fluorescent microscopy of frozen tissue sections was used to perform a detailed histological survey of the pattern of EGFP expression in these mice. Flow cytometry was also used to determine the expression pattern in blood and bone marrow.
Three patterns of EGFP expression were noted. In most tissues there was an apparently stochastic variegation of the transgene, with individual cell types demonstrating highly variable rates of EGFP expression. Certain specific cell types such as pancreatic ductal epithelium, cerebral cortical neurones and glial cells and glomerular mesangial cells consistently lacked EGFP expression, while others, including pancreatic islet cells, expressed EGFP only at extremely low levels, barely distinguishable from background. Lastly, in the colon and stomach the pattern of EGFP expression was suggestive of clonal inactivation. Only cardiac and skeletal muscle showed near ubiquitous expression.
These findings raise questions regarding the ‘ubiquitous’ expression of EGFP in these transgenic mice and suggest caution in relying overly on EGFP alone as an infallible marker of donor cell origin.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>17454756</pmid><doi>10.1080/00313020701230807</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0031-3025 |
ispartof | Pathology, 2007-04, Vol.39 (2), p.247-251 |
issn | 0031-3025 1465-3931 |
language | eng |
recordid | cdi_proquest_miscellaneous_70415924 |
source | MEDLINE; Taylor & Francis Journals Complete; Alma/SFX Local Collection |
subjects | Animals Biomedical Research - methods Cell Lineage Flow Cytometry Fluorescent Antibody Technique GFP expression GFP Mice Green Fluorescent Proteins - biosynthesis Green Fluorescent Proteins - genetics Mice Mice, Transgenic Microscopy, Fluorescence Models, Animal stem cell transplantation Stem Cells |
title | A histological survey of green fluorescent protein expression in ‘green’ mice: implications for stem cell research |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-10T03%3A49%3A42IST&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=A%20histological%20survey%20of%20green%20fluorescent%20protein%20expression%20in%20%E2%80%98green%E2%80%99%20mice:%20implications%20for%20stem%20cell%20research&rft.jtitle=Pathology&rft.au=Biankin,%20Sandra%20A.&rft.date=2007-04-01&rft.volume=39&rft.issue=2&rft.spage=247&rft.epage=251&rft.pages=247-251&rft.issn=0031-3025&rft.eissn=1465-3931&rft_id=info:doi/10.1080/00313020701230807&rft_dat=%3Cproquest_cross%3E20768834%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=20768834&rft_id=info:pmid/17454756&rft_els_id=S003130251633803X&rfr_iscdi=true |