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Characterization of factors that determine lentiviral vector tropism in skin tissue using an ex vivo model
Background Lentiviral tropism to a solid tissue may be determined by receptor availability, the differentiation state of cells and the three‐dimensional architecture of the tissue. Methods Using skin organ cultures, lentiviral vector tropism was compared with that of keratinocytes in cell culture. F...
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Published in: | The journal of gene medicine 2011-04, Vol.13 (4), p.209-220 |
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description | Background
Lentiviral tropism to a solid tissue may be determined by receptor availability, the differentiation state of cells and the three‐dimensional architecture of the tissue.
Methods
Using skin organ cultures, lentiviral vector tropism was compared with that of keratinocytes in cell culture. Furthermore, the tropism of lentiviral vector to mouse and human tissues was compared ex vivo, in attempt to validate the mouse skin as an experimental system for human gene therapy of skin diseases.
Results
The results obtained indicated that although early progenitor keratinocytes (keratin 15+ and p63+), when grown in culture are permissive to lentiviral vector, they are resistant to transduction in their native ‘niche’ in the skin tissue. Transiently amplifying keratinocytes (keratin 14+) on the other hand, are permissive to lentiviral vector transduction, in cell culture and in the skin, after separation of the epidermis from the dermis layer. Keratinocytes (keratin 14+) in the hair follicle of human skin are resistant to lentiviral transduction, even after partial digestion of the extracellular matrix collagen. By contrast, collagenase pretreatment of mouse tissue facilitated transduction of keratinocytes within the hair follicle. Because lentivirus pseudotyped by two envelopes (amphotropic murine leukemia virus and vesicular stomatitis virus G glycoprotein) display the same tropism, we suggest that receptor availability is not the critical factor in the pattern of skin tissue transduction.
Conclusions
Taken together, the results obtained in the present study indicate that lentiviral vector tropism in the three‐dimensional skin tissue is distinct from the tropism to keratinocytes in culture and is dependent on a complex interplay of extracellular restrictions. Copyright © 2011 John Wiley & Sons, Ltd. |
doi_str_mv | 10.1002/jgm.1554 |
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Lentiviral tropism to a solid tissue may be determined by receptor availability, the differentiation state of cells and the three‐dimensional architecture of the tissue.
Methods
Using skin organ cultures, lentiviral vector tropism was compared with that of keratinocytes in cell culture. Furthermore, the tropism of lentiviral vector to mouse and human tissues was compared ex vivo, in attempt to validate the mouse skin as an experimental system for human gene therapy of skin diseases.
Results
The results obtained indicated that although early progenitor keratinocytes (keratin 15+ and p63+), when grown in culture are permissive to lentiviral vector, they are resistant to transduction in their native ‘niche’ in the skin tissue. Transiently amplifying keratinocytes (keratin 14+) on the other hand, are permissive to lentiviral vector transduction, in cell culture and in the skin, after separation of the epidermis from the dermis layer. Keratinocytes (keratin 14+) in the hair follicle of human skin are resistant to lentiviral transduction, even after partial digestion of the extracellular matrix collagen. By contrast, collagenase pretreatment of mouse tissue facilitated transduction of keratinocytes within the hair follicle. Because lentivirus pseudotyped by two envelopes (amphotropic murine leukemia virus and vesicular stomatitis virus G glycoprotein) display the same tropism, we suggest that receptor availability is not the critical factor in the pattern of skin tissue transduction.
Conclusions
Taken together, the results obtained in the present study indicate that lentiviral vector tropism in the three‐dimensional skin tissue is distinct from the tropism to keratinocytes in culture and is dependent on a complex interplay of extracellular restrictions. Copyright © 2011 John Wiley & Sons, Ltd.</description><identifier>ISSN: 1099-498X</identifier><identifier>ISSN: 1521-2254</identifier><identifier>EISSN: 1521-2254</identifier><identifier>DOI: 10.1002/jgm.1554</identifier><identifier>PMID: 21416565</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Animals ; Cell Line ; Collagenases ; ex vivo ; Flow Cytometry ; Gene therapy ; Genetic Vectors - genetics ; Hair Follicle - cytology ; Hair Follicle - virology ; Humans ; Immunohistochemistry ; keratinocytes ; Keratinocytes - virology ; lentiviral vector ; Lentivirus ; Lentivirus - physiology ; Mice ; Microscopy, Fluorescence ; Murine leukemia virus ; skin ; Skin - cytology ; Skin - virology ; Transduction, Genetic ; Vesicular stomatitis virus ; Viral Tropism - physiology</subject><ispartof>The journal of gene medicine, 2011-04, Vol.13 (4), p.209-220</ispartof><rights>Copyright © 2011 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4184-91ed53cd6243a102c21db3fca448f7c8124157cecdf5c2cfe3f7fd9f6cc819523</citedby><cites>FETCH-LOGICAL-c4184-91ed53cd6243a102c21db3fca448f7c8124157cecdf5c2cfe3f7fd9f6cc819523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21416565$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kunicher, Nikolai</creatorcontrib><creatorcontrib>Tzur, Tomer</creatorcontrib><creatorcontrib>Amar, Dalit</creatorcontrib><creatorcontrib>Chaouat, Malka</creatorcontrib><creatorcontrib>Yaacov, Barak</creatorcontrib><creatorcontrib>Panet, Amos</creatorcontrib><title>Characterization of factors that determine lentiviral vector tropism in skin tissue using an ex vivo model</title><title>The journal of gene medicine</title><addtitle>J. Gene Med</addtitle><description>Background
Lentiviral tropism to a solid tissue may be determined by receptor availability, the differentiation state of cells and the three‐dimensional architecture of the tissue.
Methods
Using skin organ cultures, lentiviral vector tropism was compared with that of keratinocytes in cell culture. Furthermore, the tropism of lentiviral vector to mouse and human tissues was compared ex vivo, in attempt to validate the mouse skin as an experimental system for human gene therapy of skin diseases.
Results
The results obtained indicated that although early progenitor keratinocytes (keratin 15+ and p63+), when grown in culture are permissive to lentiviral vector, they are resistant to transduction in their native ‘niche’ in the skin tissue. Transiently amplifying keratinocytes (keratin 14+) on the other hand, are permissive to lentiviral vector transduction, in cell culture and in the skin, after separation of the epidermis from the dermis layer. Keratinocytes (keratin 14+) in the hair follicle of human skin are resistant to lentiviral transduction, even after partial digestion of the extracellular matrix collagen. By contrast, collagenase pretreatment of mouse tissue facilitated transduction of keratinocytes within the hair follicle. Because lentivirus pseudotyped by two envelopes (amphotropic murine leukemia virus and vesicular stomatitis virus G glycoprotein) display the same tropism, we suggest that receptor availability is not the critical factor in the pattern of skin tissue transduction.
Conclusions
Taken together, the results obtained in the present study indicate that lentiviral vector tropism in the three‐dimensional skin tissue is distinct from the tropism to keratinocytes in culture and is dependent on a complex interplay of extracellular restrictions. Copyright © 2011 John Wiley & Sons, Ltd.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Collagenases</subject><subject>ex vivo</subject><subject>Flow Cytometry</subject><subject>Gene therapy</subject><subject>Genetic Vectors - genetics</subject><subject>Hair Follicle - cytology</subject><subject>Hair Follicle - virology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>keratinocytes</subject><subject>Keratinocytes - virology</subject><subject>lentiviral vector</subject><subject>Lentivirus</subject><subject>Lentivirus - physiology</subject><subject>Mice</subject><subject>Microscopy, Fluorescence</subject><subject>Murine leukemia virus</subject><subject>skin</subject><subject>Skin - cytology</subject><subject>Skin - virology</subject><subject>Transduction, Genetic</subject><subject>Vesicular stomatitis virus</subject><subject>Viral Tropism - physiology</subject><issn>1099-498X</issn><issn>1521-2254</issn><issn>1521-2254</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqF0U1rFDEYB_Agiq1V8BNIwINepuZ1khxlsdtqfQNFbyHNPGmznZmsycza-unNsmsPgnhJQp4ffxL-CD2l5JgSwl6tLodjKqW4hw6pZLRhTIr79UyMaYTR3w_Qo1JWhFCltXmIDhgVtJWtPESrxZXLzk-Q4y83xTTiFHCoFykXPF25CXdQh0McAfcwTnETs-vxBrYCTzmtYxlwHHG5rssUS5kBzyWOl9iNGG7wJm4SHlIH_WP0ILi-wJP9foS-nrz5sjhtzj8uzxavzxsvqBaNodBJ7ruWCe4oYZ7R7oIH74TQQXlNmaBSefBdkJ75ADyo0JnQ-jozkvEj9GKXu87pxwxlskMsHvrejZDmYrXmhJmWqv_LlqtWUSWqfP6XXKU5j_UbliopjaiP01W93CmfUykZgl3nOLh8aymx26JsLcpui6r02T5wvhigu4N_mqmg2YGfsYfbfwbZt8v3-8C9j2WCmzvv8rVtFVfSfvuwtJ_ak8_vDCd2yX8D99msaw</recordid><startdate>201104</startdate><enddate>201104</enddate><creator>Kunicher, Nikolai</creator><creator>Tzur, Tomer</creator><creator>Amar, Dalit</creator><creator>Chaouat, Malka</creator><creator>Yaacov, Barak</creator><creator>Panet, Amos</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>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>201104</creationdate><title>Characterization of factors that determine lentiviral vector tropism in skin tissue using an ex vivo model</title><author>Kunicher, Nikolai ; Tzur, Tomer ; Amar, Dalit ; Chaouat, Malka ; Yaacov, Barak ; Panet, Amos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4184-91ed53cd6243a102c21db3fca448f7c8124157cecdf5c2cfe3f7fd9f6cc819523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Collagenases</topic><topic>ex vivo</topic><topic>Flow Cytometry</topic><topic>Gene therapy</topic><topic>Genetic Vectors - genetics</topic><topic>Hair Follicle - cytology</topic><topic>Hair Follicle - virology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>keratinocytes</topic><topic>Keratinocytes - virology</topic><topic>lentiviral vector</topic><topic>Lentivirus</topic><topic>Lentivirus - physiology</topic><topic>Mice</topic><topic>Microscopy, Fluorescence</topic><topic>Murine leukemia virus</topic><topic>skin</topic><topic>Skin - cytology</topic><topic>Skin - virology</topic><topic>Transduction, Genetic</topic><topic>Vesicular stomatitis virus</topic><topic>Viral Tropism - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kunicher, Nikolai</creatorcontrib><creatorcontrib>Tzur, Tomer</creatorcontrib><creatorcontrib>Amar, Dalit</creatorcontrib><creatorcontrib>Chaouat, Malka</creatorcontrib><creatorcontrib>Yaacov, Barak</creatorcontrib><creatorcontrib>Panet, Amos</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>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>The journal of gene medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kunicher, Nikolai</au><au>Tzur, Tomer</au><au>Amar, Dalit</au><au>Chaouat, Malka</au><au>Yaacov, Barak</au><au>Panet, Amos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of factors that determine lentiviral vector tropism in skin tissue using an ex vivo model</atitle><jtitle>The journal of gene medicine</jtitle><addtitle>J. Gene Med</addtitle><date>2011-04</date><risdate>2011</risdate><volume>13</volume><issue>4</issue><spage>209</spage><epage>220</epage><pages>209-220</pages><issn>1099-498X</issn><issn>1521-2254</issn><eissn>1521-2254</eissn><abstract>Background
Lentiviral tropism to a solid tissue may be determined by receptor availability, the differentiation state of cells and the three‐dimensional architecture of the tissue.
Methods
Using skin organ cultures, lentiviral vector tropism was compared with that of keratinocytes in cell culture. Furthermore, the tropism of lentiviral vector to mouse and human tissues was compared ex vivo, in attempt to validate the mouse skin as an experimental system for human gene therapy of skin diseases.
Results
The results obtained indicated that although early progenitor keratinocytes (keratin 15+ and p63+), when grown in culture are permissive to lentiviral vector, they are resistant to transduction in their native ‘niche’ in the skin tissue. Transiently amplifying keratinocytes (keratin 14+) on the other hand, are permissive to lentiviral vector transduction, in cell culture and in the skin, after separation of the epidermis from the dermis layer. Keratinocytes (keratin 14+) in the hair follicle of human skin are resistant to lentiviral transduction, even after partial digestion of the extracellular matrix collagen. By contrast, collagenase pretreatment of mouse tissue facilitated transduction of keratinocytes within the hair follicle. Because lentivirus pseudotyped by two envelopes (amphotropic murine leukemia virus and vesicular stomatitis virus G glycoprotein) display the same tropism, we suggest that receptor availability is not the critical factor in the pattern of skin tissue transduction.
Conclusions
Taken together, the results obtained in the present study indicate that lentiviral vector tropism in the three‐dimensional skin tissue is distinct from the tropism to keratinocytes in culture and is dependent on a complex interplay of extracellular restrictions. Copyright © 2011 John Wiley & Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><pmid>21416565</pmid><doi>10.1002/jgm.1554</doi><tpages>12</tpages></addata></record> |
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subjects | Animals Cell Line Collagenases ex vivo Flow Cytometry Gene therapy Genetic Vectors - genetics Hair Follicle - cytology Hair Follicle - virology Humans Immunohistochemistry keratinocytes Keratinocytes - virology lentiviral vector Lentivirus Lentivirus - physiology Mice Microscopy, Fluorescence Murine leukemia virus skin Skin - cytology Skin - virology Transduction, Genetic Vesicular stomatitis virus Viral Tropism - physiology |
title | Characterization of factors that determine lentiviral vector tropism in skin tissue using an ex vivo model |
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