Development of a Corneal Bioluminescence Mouse for Real-Time In Vivo Evaluation of Gene Therapies
The purpose of this study was to develop and characterize a novel bioluminescence transgenic mouse model that facilitates rapid evaluation of genetic medicine delivery methods for inherited and acquired corneal diseases. Corneal expression of the firefly luciferase transgene ( ) was achieved via ins...
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Veröffentlicht in: | Translational vision science & technology 2020-12, Vol.9 (13), p.44-44 |
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creator | Fu, Dun Jack Allen, Edwin H A Hickerson, Robyn P Leslie Pedrioli, Deena M McLean, W H Irwin |
description | The purpose of this study was to develop and characterize a novel bioluminescence transgenic mouse model that facilitates rapid evaluation of genetic medicine delivery methods for inherited and acquired corneal diseases.
Corneal expression of the firefly luciferase transgene (
) was achieved via insertion into the
locus, a type I intermediate filament keratin that is exclusively expressed in the cornea, to generate the
mouse. The transgene includes a multiple target cassette with human pathogenic mutations in K3 and K12.
The
mouse exclusively expresses
in the corneal epithelium under control of the keratin K12 promoter. The luc2 protein is enzymatically active, can be readily visualized, and exhibits a symmetrically consistent readout. Moreover, structural integrity of the corneal epithelium is preserved in mice that are heterozygous for the
transgene (
).
This novel
mouse model represents a potentially ideal in vivo system for evaluating the efficacies of cornea-targeting gene therapies and for establishing and/or validating new delivery modalities. Importantly, the multiple targeting cassette that is included in the
transgene will greatly reduce mouse numbers required for in vivo therapy evaluation. |
doi_str_mv | 10.1167/TVST.9.13.44 |
format | Article |
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Corneal expression of the firefly luciferase transgene (
) was achieved via insertion into the
locus, a type I intermediate filament keratin that is exclusively expressed in the cornea, to generate the
mouse. The transgene includes a multiple target cassette with human pathogenic mutations in K3 and K12.
The
mouse exclusively expresses
in the corneal epithelium under control of the keratin K12 promoter. The luc2 protein is enzymatically active, can be readily visualized, and exhibits a symmetrically consistent readout. Moreover, structural integrity of the corneal epithelium is preserved in mice that are heterozygous for the
transgene (
).
This novel
mouse model represents a potentially ideal in vivo system for evaluating the efficacies of cornea-targeting gene therapies and for establishing and/or validating new delivery modalities. Importantly, the multiple targeting cassette that is included in the
transgene will greatly reduce mouse numbers required for in vivo therapy evaluation.</description><identifier>ISSN: 2164-2591</identifier><identifier>EISSN: 2164-2591</identifier><identifier>DOI: 10.1167/TVST.9.13.44</identifier><identifier>PMID: 33442498</identifier><language>eng</language><publisher>United States: The Association for Research in Vision and Ophthalmology</publisher><subject>Animals ; Cornea ; Corneal Diseases - genetics ; Epithelium, Corneal ; Heterozygote ; Mice ; Mice, Transgenic</subject><ispartof>Translational vision science & technology, 2020-12, Vol.9 (13), p.44-44</ispartof><rights>Copyright 2020 The Authors.</rights><rights>Copyright 2020 The Authors 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-adf3eef0ba3e7f5f7b353277e7282c8e8c7ba6ba895ea0bbeebf08e49cbd80713</citedby><cites>FETCH-LOGICAL-c384t-adf3eef0ba3e7f5f7b353277e7282c8e8c7ba6ba895ea0bbeebf08e49cbd80713</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774114/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774114/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33442498$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fu, Dun Jack</creatorcontrib><creatorcontrib>Allen, Edwin H A</creatorcontrib><creatorcontrib>Hickerson, Robyn P</creatorcontrib><creatorcontrib>Leslie Pedrioli, Deena M</creatorcontrib><creatorcontrib>McLean, W H Irwin</creatorcontrib><title>Development of a Corneal Bioluminescence Mouse for Real-Time In Vivo Evaluation of Gene Therapies</title><title>Translational vision science & technology</title><addtitle>Transl Vis Sci Technol</addtitle><description>The purpose of this study was to develop and characterize a novel bioluminescence transgenic mouse model that facilitates rapid evaluation of genetic medicine delivery methods for inherited and acquired corneal diseases.
Corneal expression of the firefly luciferase transgene (
) was achieved via insertion into the
locus, a type I intermediate filament keratin that is exclusively expressed in the cornea, to generate the
mouse. The transgene includes a multiple target cassette with human pathogenic mutations in K3 and K12.
The
mouse exclusively expresses
in the corneal epithelium under control of the keratin K12 promoter. The luc2 protein is enzymatically active, can be readily visualized, and exhibits a symmetrically consistent readout. Moreover, structural integrity of the corneal epithelium is preserved in mice that are heterozygous for the
transgene (
).
This novel
mouse model represents a potentially ideal in vivo system for evaluating the efficacies of cornea-targeting gene therapies and for establishing and/or validating new delivery modalities. Importantly, the multiple targeting cassette that is included in the
transgene will greatly reduce mouse numbers required for in vivo therapy evaluation.</description><subject>Animals</subject><subject>Cornea</subject><subject>Corneal Diseases - genetics</subject><subject>Epithelium, Corneal</subject><subject>Heterozygote</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><issn>2164-2591</issn><issn>2164-2591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU1LxDAQhoMoKurNs-Towa5JkzbpRdD1ExRBq9eQdCcaaZM1aQv-e7v4gc5lBt53nplhENqnZEZpKY7r58d6Vs0om3G-hrZzWvIsLyq6_qfeQnspvZEpSllwXm6iLcY4z3klt5E-hxHasOzA9zhYrPE8RA-6xWcutEPnPKQGfAP4LgwJsA0RP0xyVrsO8I3Hz24M-GLU7aB7F_yKcQUecP0KUS8dpF20YXWbYO8776Cny4t6fp3d3l_dzE9vs4ZJ3md6YRmAJUYzELawwrCC5UKAyGXeSJCNMLo0WlYFaGIMgLFEAq8as5BEULaDTr64y8F0sJiW7qNu1TK6TscPFbRT_xXvXtVLGJUQglPKJ8DhNyCG9wFSrzo33d622sN0u8q5kISVBWGT9ejL2sSQUgT7O4YStXqM6sepv1KUKb4iH_xd7df88wb2CcIdjAo</recordid><startdate>20201201</startdate><enddate>20201201</enddate><creator>Fu, Dun Jack</creator><creator>Allen, Edwin H A</creator><creator>Hickerson, Robyn P</creator><creator>Leslie Pedrioli, Deena M</creator><creator>McLean, W H Irwin</creator><general>The Association for Research in Vision and Ophthalmology</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20201201</creationdate><title>Development of a Corneal Bioluminescence Mouse for Real-Time In Vivo Evaluation of Gene Therapies</title><author>Fu, Dun Jack ; Allen, Edwin H A ; Hickerson, Robyn P ; Leslie Pedrioli, Deena M ; McLean, W H Irwin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-adf3eef0ba3e7f5f7b353277e7282c8e8c7ba6ba895ea0bbeebf08e49cbd80713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cornea</topic><topic>Corneal Diseases - genetics</topic><topic>Epithelium, Corneal</topic><topic>Heterozygote</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fu, Dun Jack</creatorcontrib><creatorcontrib>Allen, Edwin H A</creatorcontrib><creatorcontrib>Hickerson, Robyn P</creatorcontrib><creatorcontrib>Leslie Pedrioli, Deena M</creatorcontrib><creatorcontrib>McLean, W H Irwin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Translational vision science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fu, Dun Jack</au><au>Allen, Edwin H A</au><au>Hickerson, Robyn P</au><au>Leslie Pedrioli, Deena M</au><au>McLean, W H Irwin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development of a Corneal Bioluminescence Mouse for Real-Time In Vivo Evaluation of Gene Therapies</atitle><jtitle>Translational vision science & technology</jtitle><addtitle>Transl Vis Sci Technol</addtitle><date>2020-12-01</date><risdate>2020</risdate><volume>9</volume><issue>13</issue><spage>44</spage><epage>44</epage><pages>44-44</pages><issn>2164-2591</issn><eissn>2164-2591</eissn><abstract>The purpose of this study was to develop and characterize a novel bioluminescence transgenic mouse model that facilitates rapid evaluation of genetic medicine delivery methods for inherited and acquired corneal diseases.
Corneal expression of the firefly luciferase transgene (
) was achieved via insertion into the
locus, a type I intermediate filament keratin that is exclusively expressed in the cornea, to generate the
mouse. The transgene includes a multiple target cassette with human pathogenic mutations in K3 and K12.
The
mouse exclusively expresses
in the corneal epithelium under control of the keratin K12 promoter. The luc2 protein is enzymatically active, can be readily visualized, and exhibits a symmetrically consistent readout. Moreover, structural integrity of the corneal epithelium is preserved in mice that are heterozygous for the
transgene (
).
This novel
mouse model represents a potentially ideal in vivo system for evaluating the efficacies of cornea-targeting gene therapies and for establishing and/or validating new delivery modalities. Importantly, the multiple targeting cassette that is included in the
transgene will greatly reduce mouse numbers required for in vivo therapy evaluation.</abstract><cop>United States</cop><pub>The Association for Research in Vision and Ophthalmology</pub><pmid>33442498</pmid><doi>10.1167/TVST.9.13.44</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central |
subjects | Animals Cornea Corneal Diseases - genetics Epithelium, Corneal Heterozygote Mice Mice, Transgenic |
title | Development of a Corneal Bioluminescence Mouse for Real-Time In Vivo Evaluation of Gene Therapies |
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