Somatic gene transfer into the lactating ovine mammary gland
Background Somatic gene therapy requires safe and efficient techniques for the gene transfer procedure. The ovine mammary gland is described as a model system for the evaluation of somatic gene transfer methods. Methods Different gene delivery formulations were retrogradely injected into the mammary...
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Veröffentlicht in: | The journal of gene medicine 2002-05, Vol.4 (3), p.282-291 |
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creator | Düchler, Markus Pengg, Margret Schüller, Susanne Pfneisl, Franz Bugingo, Christoph Brem, Gottfried Wagner, Ernst Schellander, Karl Müller, Mathias |
description | Background
Somatic gene therapy requires safe and efficient techniques for the gene transfer procedure. The ovine mammary gland is described as a model system for the evaluation of somatic gene transfer methods.
Methods
Different gene delivery formulations were retrogradely injected into the mammary gland of lactating sheep. The efficiency of the gene transfer was subsequently measured by the detection of the secreted transgene products in the milk. To counteract the milk flow in the lactating gland caused by the permanent milk production, a newly developed pretreatment of the mammary gland with hyperosmotic solutions was applied. In addition, in vivo electroporation of DNA into the mammary gland is described.
Results
Gene transfer using naked DNA or simple complexes of DNA with polycations did not result in traceable amounts of reporter gene products. However, utilizing the complex cationic lipid DOSPER, a peak expression of about 400 ng/ml was observed 6 days after transfection. Maximum expression rates of more than 1 µg/ml were obtained by combining hyperosmotic pretreatment and receptor‐mediated gene transfer. For the in vivo electroporation, the proof of principle for this technique in the mammary gland is reported.
Conclusions
The ovine mammary gland turned out to be a very well suited as a model system for evaluation and optimization of various gene transfer protocols. Copyright © 2002 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jgm.272 |
format | Article |
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Somatic gene therapy requires safe and efficient techniques for the gene transfer procedure. The ovine mammary gland is described as a model system for the evaluation of somatic gene transfer methods.
Methods
Different gene delivery formulations were retrogradely injected into the mammary gland of lactating sheep. The efficiency of the gene transfer was subsequently measured by the detection of the secreted transgene products in the milk. To counteract the milk flow in the lactating gland caused by the permanent milk production, a newly developed pretreatment of the mammary gland with hyperosmotic solutions was applied. In addition, in vivo electroporation of DNA into the mammary gland is described.
Results
Gene transfer using naked DNA or simple complexes of DNA with polycations did not result in traceable amounts of reporter gene products. However, utilizing the complex cationic lipid DOSPER, a peak expression of about 400 ng/ml was observed 6 days after transfection. Maximum expression rates of more than 1 µg/ml were obtained by combining hyperosmotic pretreatment and receptor‐mediated gene transfer. For the in vivo electroporation, the proof of principle for this technique in the mammary gland is reported.
Conclusions
The ovine mammary gland turned out to be a very well suited as a model system for evaluation and optimization of various gene transfer protocols. Copyright © 2002 John Wiley & Sons, Ltd.</description><identifier>ISSN: 1099-498X</identifier><identifier>EISSN: 1521-2254</identifier><identifier>DOI: 10.1002/jgm.272</identifier><identifier>PMID: 12112645</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Animals ; Electroporation ; Enzyme-Linked Immunosorbent Assay ; Female ; Gene therapy ; Gene Transfer Techniques ; Genes, Reporter ; in vivo electroporation ; in vivo or somatic gene transfer ; Lactation ; Mammary Glands, Animal - anatomy & histology ; Mammary Glands, Animal - metabolism ; Osmolar Concentration ; ovine mammary gland ; Sheep ; Solutions ; Transfection</subject><ispartof>The journal of gene medicine, 2002-05, Vol.4 (3), p.282-291</ispartof><rights>Copyright © 2002 John Wiley & Sons, Ltd.</rights><rights>Copyright 2002 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4092-6d10155c89562c8eca3072a047740ed6193687f2a9a4920da365f06b018377dd3</citedby><cites>FETCH-LOGICAL-c4092-6d10155c89562c8eca3072a047740ed6193687f2a9a4920da365f06b018377dd3</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%2Fjgm.272$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjgm.272$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12112645$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Düchler, Markus</creatorcontrib><creatorcontrib>Pengg, Margret</creatorcontrib><creatorcontrib>Schüller, Susanne</creatorcontrib><creatorcontrib>Pfneisl, Franz</creatorcontrib><creatorcontrib>Bugingo, Christoph</creatorcontrib><creatorcontrib>Brem, Gottfried</creatorcontrib><creatorcontrib>Wagner, Ernst</creatorcontrib><creatorcontrib>Schellander, Karl</creatorcontrib><creatorcontrib>Müller, Mathias</creatorcontrib><title>Somatic gene transfer into the lactating ovine mammary gland</title><title>The journal of gene medicine</title><addtitle>J. Gene Med</addtitle><description>Background
Somatic gene therapy requires safe and efficient techniques for the gene transfer procedure. The ovine mammary gland is described as a model system for the evaluation of somatic gene transfer methods.
Methods
Different gene delivery formulations were retrogradely injected into the mammary gland of lactating sheep. The efficiency of the gene transfer was subsequently measured by the detection of the secreted transgene products in the milk. To counteract the milk flow in the lactating gland caused by the permanent milk production, a newly developed pretreatment of the mammary gland with hyperosmotic solutions was applied. In addition, in vivo electroporation of DNA into the mammary gland is described.
Results
Gene transfer using naked DNA or simple complexes of DNA with polycations did not result in traceable amounts of reporter gene products. However, utilizing the complex cationic lipid DOSPER, a peak expression of about 400 ng/ml was observed 6 days after transfection. Maximum expression rates of more than 1 µg/ml were obtained by combining hyperosmotic pretreatment and receptor‐mediated gene transfer. For the in vivo electroporation, the proof of principle for this technique in the mammary gland is reported.
Conclusions
The ovine mammary gland turned out to be a very well suited as a model system for evaluation and optimization of various gene transfer protocols. Copyright © 2002 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>Electroporation</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Gene therapy</subject><subject>Gene Transfer Techniques</subject><subject>Genes, Reporter</subject><subject>in vivo electroporation</subject><subject>in vivo or somatic gene transfer</subject><subject>Lactation</subject><subject>Mammary Glands, Animal - anatomy & histology</subject><subject>Mammary Glands, Animal - metabolism</subject><subject>Osmolar Concentration</subject><subject>ovine mammary gland</subject><subject>Sheep</subject><subject>Solutions</subject><subject>Transfection</subject><issn>1099-498X</issn><issn>1521-2254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqF0MtKAzEUBuAgipcqvoEMLnQhozmZXMGNFK13FyrtLqQzmTp1LjWZenl7I1MUBHGVA_n4k_MjtA34EDAmR9NJdUgEWULrwAjEhDC6HGasVEyVHK2hDe-nGIOQUq2iNSAAhFO2jo7vm8q0RRpNbG2j1pna59ZFRd02Uftko9KkbbivJ1HzWgRRmaoy7iOalKbONtFKbkpvtxZnDz2enT70z-Pru8FF_-Q6TilWJOYZYGAslYpxkkqbmgQLYjAVgmKbcVAJlyInRhmqCM5MwlmO-RiDTITIsqSH9rrcmWte5ta3uip8asvwB9vMvRagghX8XwiSMoHDez20-wtOm7mrwxIaFFdAuZQB7XcodY33zuZ65oqv7TVg_VW7DrXrUHuQO4u4-biy2Y9b9BzAQQfeitJ-_JWjLwc3XVzc6cK39v1bG_esuUgE08PbgWaj_lDwEeir5BPwZJdA</recordid><startdate>200205</startdate><enddate>200205</enddate><creator>Düchler, Markus</creator><creator>Pengg, Margret</creator><creator>Schüller, Susanne</creator><creator>Pfneisl, Franz</creator><creator>Bugingo, Christoph</creator><creator>Brem, Gottfried</creator><creator>Wagner, Ernst</creator><creator>Schellander, Karl</creator><creator>Müller, Mathias</creator><general>John Wiley & Sons, Ltd</general><general>Wiley Periodicals 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>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>200205</creationdate><title>Somatic gene transfer into the lactating ovine mammary gland</title><author>Düchler, Markus ; Pengg, Margret ; Schüller, Susanne ; Pfneisl, Franz ; Bugingo, Christoph ; Brem, Gottfried ; Wagner, Ernst ; Schellander, Karl ; Müller, Mathias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4092-6d10155c89562c8eca3072a047740ed6193687f2a9a4920da365f06b018377dd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Animals</topic><topic>Electroporation</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Gene therapy</topic><topic>Gene Transfer Techniques</topic><topic>Genes, Reporter</topic><topic>in vivo electroporation</topic><topic>in vivo or somatic gene transfer</topic><topic>Lactation</topic><topic>Mammary Glands, Animal - anatomy & histology</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>Osmolar Concentration</topic><topic>ovine mammary gland</topic><topic>Sheep</topic><topic>Solutions</topic><topic>Transfection</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Düchler, Markus</creatorcontrib><creatorcontrib>Pengg, Margret</creatorcontrib><creatorcontrib>Schüller, Susanne</creatorcontrib><creatorcontrib>Pfneisl, Franz</creatorcontrib><creatorcontrib>Bugingo, Christoph</creatorcontrib><creatorcontrib>Brem, Gottfried</creatorcontrib><creatorcontrib>Wagner, Ernst</creatorcontrib><creatorcontrib>Schellander, Karl</creatorcontrib><creatorcontrib>Müller, Mathias</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>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of gene medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Düchler, Markus</au><au>Pengg, Margret</au><au>Schüller, Susanne</au><au>Pfneisl, Franz</au><au>Bugingo, Christoph</au><au>Brem, Gottfried</au><au>Wagner, Ernst</au><au>Schellander, Karl</au><au>Müller, Mathias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Somatic gene transfer into the lactating ovine mammary gland</atitle><jtitle>The journal of gene medicine</jtitle><addtitle>J. Gene Med</addtitle><date>2002-05</date><risdate>2002</risdate><volume>4</volume><issue>3</issue><spage>282</spage><epage>291</epage><pages>282-291</pages><issn>1099-498X</issn><eissn>1521-2254</eissn><abstract>Background
Somatic gene therapy requires safe and efficient techniques for the gene transfer procedure. The ovine mammary gland is described as a model system for the evaluation of somatic gene transfer methods.
Methods
Different gene delivery formulations were retrogradely injected into the mammary gland of lactating sheep. The efficiency of the gene transfer was subsequently measured by the detection of the secreted transgene products in the milk. To counteract the milk flow in the lactating gland caused by the permanent milk production, a newly developed pretreatment of the mammary gland with hyperosmotic solutions was applied. In addition, in vivo electroporation of DNA into the mammary gland is described.
Results
Gene transfer using naked DNA or simple complexes of DNA with polycations did not result in traceable amounts of reporter gene products. However, utilizing the complex cationic lipid DOSPER, a peak expression of about 400 ng/ml was observed 6 days after transfection. Maximum expression rates of more than 1 µg/ml were obtained by combining hyperosmotic pretreatment and receptor‐mediated gene transfer. For the in vivo electroporation, the proof of principle for this technique in the mammary gland is reported.
Conclusions
The ovine mammary gland turned out to be a very well suited as a model system for evaluation and optimization of various gene transfer protocols. Copyright © 2002 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>12112645</pmid><doi>10.1002/jgm.272</doi><tpages>10</tpages></addata></record> |
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subjects | Animals Electroporation Enzyme-Linked Immunosorbent Assay Female Gene therapy Gene Transfer Techniques Genes, Reporter in vivo electroporation in vivo or somatic gene transfer Lactation Mammary Glands, Animal - anatomy & histology Mammary Glands, Animal - metabolism Osmolar Concentration ovine mammary gland Sheep Solutions Transfection |
title | Somatic gene transfer into the lactating ovine mammary gland |
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