<it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectors

<p>Abstract</p> <p>Background</p> <p>For both <it>in vitro </it>and <it>in vivo </it>gene transfer applications, recombinant viral vectors have almost always been used free in solution. Some site-specificity of the delivery of viral vectors can b...

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Main Authors: Pandori Mark W, Hobson David A, Sano Takeshi
Format: Article
Language:English
Published: BMC 2003-05-01
Series:BMC Biotechnology
Online Access:http://www.biomedcentral.com/1472-6750/3/4
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spelling doaj-35c52acea99e470c93a1c7ead11847312020-11-25T03:42:51ZengBMCBMC Biotechnology1472-67502003-05-0131410.1186/1472-6750-3-4<it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectorsPandori Mark WHobson David ASano Takeshi<p>Abstract</p> <p>Background</p> <p>For both <it>in vitro </it>and <it>in vivo </it>gene transfer applications, recombinant viral vectors have almost always been used free in solution. Some site-specificity of the delivery of viral vectors can be achieved by applying a solution containing viral particles specifically to the site of interest. However, such site-specificity is seriously limited since viral vectors can diffuse freely in solution after application.</p> <p>Results</p> <p>We have developed a novel strategy for <it>in situ </it>transduction of target cells on solid surfaces by viral vectors. In this strategy, adenoviral vectors are attached stably to solid surfaces by using the extremely tight interaction between (strept)avidin and biotin, while maintaining the infectivity of the viral vectors. Target cells are cultured directly on such virus-coated solid surfaces, resulting in the transduction of the cells, <it>in situ</it>, on the solid surface. When compared using an equal number of viral particles present in each well (either immobilized or free), the efficiencies of such <it>in situ </it>transduction on solid surfaces were equivalent to those seen with the adenoviral vectors used free in solution. Since viral particles can be attached at desired locations on solid surfaces in any sizes, shapes, and patterns, the ultimate spatial arrangements of transduced cells on solid surfaces can be predetermined at the time of the preparation of the virus-coated solid surfaces.</p> <p>Conclusions</p> <p>We have devised a method of immobilizing adenoviral vectors, tightly and stably, on solid surfaces, while maintaining their ability to infect cells. Such immobilized viral vectors can infect target cells, <it>in situ</it>, on solid surfaces. This strategy should be very useful for the development of a variety of both <it>in vitro </it>and <it>in vivo </it>applications, including the creation of cell-based expression arrays for proteomics and drug discovery and highly site-specific delivery of transgenes for gene therapy and tissue engineering.</p> http://www.biomedcentral.com/1472-6750/3/4
collection DOAJ
language English
format Article
sources DOAJ
author Pandori Mark W
Hobson David A
Sano Takeshi
spellingShingle Pandori Mark W
Hobson David A
Sano Takeshi
<it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectors
BMC Biotechnology
author_facet Pandori Mark W
Hobson David A
Sano Takeshi
author_sort Pandori Mark W
title <it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectors
title_short <it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectors
title_full <it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectors
title_fullStr <it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectors
title_full_unstemmed <it>In situ </it>transduction of target cells on solid surfaces by immobilized viral vectors
title_sort <it>in situ </it>transduction of target cells on solid surfaces by immobilized viral vectors
publisher BMC
series BMC Biotechnology
issn 1472-6750
publishDate 2003-05-01
description <p>Abstract</p> <p>Background</p> <p>For both <it>in vitro </it>and <it>in vivo </it>gene transfer applications, recombinant viral vectors have almost always been used free in solution. Some site-specificity of the delivery of viral vectors can be achieved by applying a solution containing viral particles specifically to the site of interest. However, such site-specificity is seriously limited since viral vectors can diffuse freely in solution after application.</p> <p>Results</p> <p>We have developed a novel strategy for <it>in situ </it>transduction of target cells on solid surfaces by viral vectors. In this strategy, adenoviral vectors are attached stably to solid surfaces by using the extremely tight interaction between (strept)avidin and biotin, while maintaining the infectivity of the viral vectors. Target cells are cultured directly on such virus-coated solid surfaces, resulting in the transduction of the cells, <it>in situ</it>, on the solid surface. When compared using an equal number of viral particles present in each well (either immobilized or free), the efficiencies of such <it>in situ </it>transduction on solid surfaces were equivalent to those seen with the adenoviral vectors used free in solution. Since viral particles can be attached at desired locations on solid surfaces in any sizes, shapes, and patterns, the ultimate spatial arrangements of transduced cells on solid surfaces can be predetermined at the time of the preparation of the virus-coated solid surfaces.</p> <p>Conclusions</p> <p>We have devised a method of immobilizing adenoviral vectors, tightly and stably, on solid surfaces, while maintaining their ability to infect cells. Such immobilized viral vectors can infect target cells, <it>in situ</it>, on solid surfaces. This strategy should be very useful for the development of a variety of both <it>in vitro </it>and <it>in vivo </it>applications, including the creation of cell-based expression arrays for proteomics and drug discovery and highly site-specific delivery of transgenes for gene therapy and tissue engineering.</p>
url http://www.biomedcentral.com/1472-6750/3/4
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