Intramuscular plasmid DNA electrotransfer: Biodistribution and degradation
We have studied radiolabelled plasmid DNA biodistribution and degradation in the muscle at different times after injection, with or without electrotransfer using previously defined conditions. Radiolabelled plasmid progressively left the muscle and was degraded as soon as 5 min after plasmid injecti...
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description | We have studied radiolabelled plasmid DNA biodistribution and degradation in the muscle at different times after injection, with or without electrotransfer using previously defined conditions. Radiolabelled plasmid progressively left the muscle and was degraded as soon as 5 min after plasmid injection, with or without electrotransfer. Autoradiography showed that the major part of injected radioactivity was detected in the interfibrilar space of a large proportion of the muscle. Large zones of accumulation of radioactivity, which seems to be contained in some fibres (more than 20 μm), were identified as soon as 5 min after electrotransfer. Such structures were never observed on slices of non-electrotransferred muscles. However, these structures were not frequent and probably lesional. The surprising fact is that despite the amount of intact plasmid having been greatly reduced between 5 min and 3 h after injection, the level of transfection remains unchanged whether electric pulses were delivered 20 s or 3 h after injection. Such a behavior was similarly observed when injecting 0.3, 3 or 30 μg of plasmid DNA. Moreover, the transfection level was correlated to the amount of plasmid DNA injected. These results suggest that as soon as it is injected, plasmid DNA is proportionally partitioned between at least two compartments. While a major part of plasmid DNA is rapidly cleared and degraded, the electrotransferable pool of plasmid DNA represents a very small part of the amount injected and belongs to another compartment where it is protected from endogenous DNAses. |
doi_str_mv | 10.1016/j.bbaexp.2003.11.005 |
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Radiolabelled plasmid progressively left the muscle and was degraded as soon as 5 min after plasmid injection, with or without electrotransfer. Autoradiography showed that the major part of injected radioactivity was detected in the interfibrilar space of a large proportion of the muscle. Large zones of accumulation of radioactivity, which seems to be contained in some fibres (more than 20 μm), were identified as soon as 5 min after electrotransfer. Such structures were never observed on slices of non-electrotransferred muscles. However, these structures were not frequent and probably lesional. The surprising fact is that despite the amount of intact plasmid having been greatly reduced between 5 min and 3 h after injection, the level of transfection remains unchanged whether electric pulses were delivered 20 s or 3 h after injection. Such a behavior was similarly observed when injecting 0.3, 3 or 30 μg of plasmid DNA. Moreover, the transfection level was correlated to the amount of plasmid DNA injected. These results suggest that as soon as it is injected, plasmid DNA is proportionally partitioned between at least two compartments. While a major part of plasmid DNA is rapidly cleared and degraded, the electrotransferable pool of plasmid DNA represents a very small part of the amount injected and belongs to another compartment where it is protected from endogenous DNAses.</description><identifier>ISSN: 0167-4781</identifier><identifier>ISSN: 0006-3002</identifier><identifier>EISSN: 1879-2634</identifier><identifier>DOI: 10.1016/j.bbaexp.2003.11.005</identifier><identifier>PMID: 14746908</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Autoradiography ; Biodistribution ; Deoxyribonuclease I - pharmacology ; DNA - analysis ; DNA - isolation & purification ; DNA - metabolism ; DNA degradation ; Electrophoresis ; Electroporation ; electrotransfer ; Female ; Gene Amplification ; Genes, Reporter ; Injections, Intramuscular ; Mice ; Mice, Inbred C57BL ; Muscle ; Muscle Fibers, Skeletal - chemistry ; Muscle Fibers, Skeletal - metabolism ; Muscle, Skeletal - metabolism ; Plasmid DNA ; Plasmids - administration & dosage ; Plasmids - analysis ; Plasmids - pharmacology ; Time Factors ; Transfection ; Transfection - methods ; Tritium - analysis</subject><ispartof>Biochimica et biophysica acta, 2004-01, Vol.1676 (2), p.138-148</ispartof><rights>2003 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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/14746908$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bureau, M.F</creatorcontrib><creatorcontrib>Naimi, S</creatorcontrib><creatorcontrib>Torero Ibad, R</creatorcontrib><creatorcontrib>Seguin, J</creatorcontrib><creatorcontrib>Georger, C</creatorcontrib><creatorcontrib>Arnould, E</creatorcontrib><creatorcontrib>Maton, L</creatorcontrib><creatorcontrib>Blanche, F</creatorcontrib><creatorcontrib>Delaere, P</creatorcontrib><creatorcontrib>Scherman, D</creatorcontrib><title>Intramuscular plasmid DNA electrotransfer: Biodistribution and degradation</title><title>Biochimica et biophysica acta</title><addtitle>Biochim Biophys Acta</addtitle><description>We have studied radiolabelled plasmid DNA biodistribution and degradation in the muscle at different times after injection, with or without electrotransfer using previously defined conditions. Radiolabelled plasmid progressively left the muscle and was degraded as soon as 5 min after plasmid injection, with or without electrotransfer. Autoradiography showed that the major part of injected radioactivity was detected in the interfibrilar space of a large proportion of the muscle. Large zones of accumulation of radioactivity, which seems to be contained in some fibres (more than 20 μm), were identified as soon as 5 min after electrotransfer. Such structures were never observed on slices of non-electrotransferred muscles. However, these structures were not frequent and probably lesional. The surprising fact is that despite the amount of intact plasmid having been greatly reduced between 5 min and 3 h after injection, the level of transfection remains unchanged whether electric pulses were delivered 20 s or 3 h after injection. Such a behavior was similarly observed when injecting 0.3, 3 or 30 μg of plasmid DNA. Moreover, the transfection level was correlated to the amount of plasmid DNA injected. These results suggest that as soon as it is injected, plasmid DNA is proportionally partitioned between at least two compartments. While a major part of plasmid DNA is rapidly cleared and degraded, the electrotransferable pool of plasmid DNA represents a very small part of the amount injected and belongs to another compartment where it is protected from endogenous DNAses.</description><subject>Animals</subject><subject>Autoradiography</subject><subject>Biodistribution</subject><subject>Deoxyribonuclease I - pharmacology</subject><subject>DNA - analysis</subject><subject>DNA - isolation & purification</subject><subject>DNA - metabolism</subject><subject>DNA degradation</subject><subject>Electrophoresis</subject><subject>Electroporation</subject><subject>electrotransfer</subject><subject>Female</subject><subject>Gene Amplification</subject><subject>Genes, Reporter</subject><subject>Injections, Intramuscular</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Muscle</subject><subject>Muscle Fibers, Skeletal - chemistry</subject><subject>Muscle Fibers, Skeletal - metabolism</subject><subject>Muscle, Skeletal - metabolism</subject><subject>Plasmid DNA</subject><subject>Plasmids - administration & dosage</subject><subject>Plasmids - analysis</subject><subject>Plasmids - pharmacology</subject><subject>Time Factors</subject><subject>Transfection</subject><subject>Transfection - methods</subject><subject>Tritium - analysis</subject><issn>0167-4781</issn><issn>0006-3002</issn><issn>1879-2634</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkclOAzEMQCMEoqXwBwjNidsMWWZJOCCVshVVcIFzlMVFqWYjmUHw96RqOeOLZfnJlv0QOic4I5iUV5tMawXffUYxZhkhGcbFAZoSXomUliw_RNOIVWlecTJBJyFscIySlMdoQvIqLwXmU_S8bAevmjGYsVY-6WsVGmeTu5d5AjWYwXex3YY1-Ovk1nXWhcE7PQ6uaxPV2sTCh1dWbetTdLRWdYCzfZ6h94f7t8VTunp9XC7mqxSoYEMquDC2UFoQwbGgzBiGbWm4Bmy4qDjLLaVsLbTIWUGNwQXTkBcl07iinDE2Q5e7ub3vPkcIg2xcMFDXqoVuDJJjQgmN6H8giduLqqwieLEHR92Alb13jfI_8u9NEbjZARDv-nLgZTAOWgPW-fgkaTsnCZZbL3Ijd17k1oskREYv7Be5XYBB</recordid><startdate>20040120</startdate><enddate>20040120</enddate><creator>Bureau, M.F</creator><creator>Naimi, S</creator><creator>Torero Ibad, R</creator><creator>Seguin, J</creator><creator>Georger, C</creator><creator>Arnould, E</creator><creator>Maton, L</creator><creator>Blanche, F</creator><creator>Delaere, P</creator><creator>Scherman, D</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>20040120</creationdate><title>Intramuscular plasmid DNA electrotransfer: Biodistribution and degradation</title><author>Bureau, M.F ; Naimi, S ; Torero Ibad, R ; Seguin, J ; Georger, C ; Arnould, E ; Maton, L ; Blanche, F ; Delaere, P ; Scherman, D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e293t-989cd5ab91980923cc30d6c8be0c897834d223f9b94352cc053be4563b0728333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Autoradiography</topic><topic>Biodistribution</topic><topic>Deoxyribonuclease I - pharmacology</topic><topic>DNA - analysis</topic><topic>DNA - isolation & purification</topic><topic>DNA - metabolism</topic><topic>DNA degradation</topic><topic>Electrophoresis</topic><topic>Electroporation</topic><topic>electrotransfer</topic><topic>Female</topic><topic>Gene Amplification</topic><topic>Genes, Reporter</topic><topic>Injections, Intramuscular</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Muscle</topic><topic>Muscle Fibers, Skeletal - chemistry</topic><topic>Muscle Fibers, Skeletal - metabolism</topic><topic>Muscle, Skeletal - metabolism</topic><topic>Plasmid DNA</topic><topic>Plasmids - administration & dosage</topic><topic>Plasmids - analysis</topic><topic>Plasmids - pharmacology</topic><topic>Time Factors</topic><topic>Transfection</topic><topic>Transfection - methods</topic><topic>Tritium - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bureau, M.F</creatorcontrib><creatorcontrib>Naimi, S</creatorcontrib><creatorcontrib>Torero Ibad, R</creatorcontrib><creatorcontrib>Seguin, J</creatorcontrib><creatorcontrib>Georger, C</creatorcontrib><creatorcontrib>Arnould, E</creatorcontrib><creatorcontrib>Maton, L</creatorcontrib><creatorcontrib>Blanche, F</creatorcontrib><creatorcontrib>Delaere, P</creatorcontrib><creatorcontrib>Scherman, D</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimica et biophysica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bureau, M.F</au><au>Naimi, S</au><au>Torero Ibad, R</au><au>Seguin, J</au><au>Georger, C</au><au>Arnould, E</au><au>Maton, L</au><au>Blanche, F</au><au>Delaere, P</au><au>Scherman, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intramuscular plasmid DNA electrotransfer: Biodistribution and degradation</atitle><jtitle>Biochimica et biophysica acta</jtitle><addtitle>Biochim Biophys Acta</addtitle><date>2004-01-20</date><risdate>2004</risdate><volume>1676</volume><issue>2</issue><spage>138</spage><epage>148</epage><pages>138-148</pages><issn>0167-4781</issn><issn>0006-3002</issn><eissn>1879-2634</eissn><abstract>We have studied radiolabelled plasmid DNA biodistribution and degradation in the muscle at different times after injection, with or without electrotransfer using previously defined conditions. Radiolabelled plasmid progressively left the muscle and was degraded as soon as 5 min after plasmid injection, with or without electrotransfer. Autoradiography showed that the major part of injected radioactivity was detected in the interfibrilar space of a large proportion of the muscle. Large zones of accumulation of radioactivity, which seems to be contained in some fibres (more than 20 μm), were identified as soon as 5 min after electrotransfer. Such structures were never observed on slices of non-electrotransferred muscles. However, these structures were not frequent and probably lesional. The surprising fact is that despite the amount of intact plasmid having been greatly reduced between 5 min and 3 h after injection, the level of transfection remains unchanged whether electric pulses were delivered 20 s or 3 h after injection. Such a behavior was similarly observed when injecting 0.3, 3 or 30 μg of plasmid DNA. Moreover, the transfection level was correlated to the amount of plasmid DNA injected. These results suggest that as soon as it is injected, plasmid DNA is proportionally partitioned between at least two compartments. While a major part of plasmid DNA is rapidly cleared and degraded, the electrotransferable pool of plasmid DNA represents a very small part of the amount injected and belongs to another compartment where it is protected from endogenous DNAses.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>14746908</pmid><doi>10.1016/j.bbaexp.2003.11.005</doi><tpages>11</tpages></addata></record> |
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subjects | Animals Autoradiography Biodistribution Deoxyribonuclease I - pharmacology DNA - analysis DNA - isolation & purification DNA - metabolism DNA degradation Electrophoresis Electroporation electrotransfer Female Gene Amplification Genes, Reporter Injections, Intramuscular Mice Mice, Inbred C57BL Muscle Muscle Fibers, Skeletal - chemistry Muscle Fibers, Skeletal - metabolism Muscle, Skeletal - metabolism Plasmid DNA Plasmids - administration & dosage Plasmids - analysis Plasmids - pharmacology Time Factors Transfection Transfection - methods Tritium - analysis |
title | Intramuscular plasmid DNA electrotransfer: Biodistribution and degradation |
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