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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Veröffentlicht in:Biochimica et biophysica acta 2004-01, Vol.1676 (2), p.138-148
Hauptverfasser: Bureau, M.F, Naimi, S, Torero Ibad, R, Seguin, J, Georger, C, Arnould, E, Maton, L, Blanche, F, Delaere, P, Scherman, D
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container_issue 2
container_start_page 138
container_title Biochimica et biophysica acta
container_volume 1676
creator Bureau, M.F
Naimi, S
Torero Ibad, R
Seguin, J
Georger, C
Arnould, E
Maton, L
Blanche, F
Delaere, P
Scherman, D
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. 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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 ; 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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. 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source MEDLINE; Alma/SFX Local Collection
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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