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Combination of Electroporation and DNA/Dendrimer Complexes Enhances Gene Transfer into Murine Cardiac Transplants

dc.contributor.authorWang, Yinongen_US
dc.contributor.authorBai, Yalaien_US
dc.contributor.authorPrice, Christopheren_US
dc.contributor.authorBoros, Peteren_US
dc.contributor.authorQin, Lihuien_US
dc.contributor.authorBielinska, Anna U.en_US
dc.contributor.authorKukowska-Latallo, Jolanta F.en_US
dc.contributor.authorBaker, James R. Jr.en_US
dc.contributor.authorBromberg, Jonathan S.en_US
dc.date.accessioned2010-06-01T21:20:51Z
dc.date.available2010-06-01T21:20:51Z
dc.date.issued2001-11en_US
dc.identifier.citationWang, Yinong; Bai, Yalai; Price, Christopher; Boros, Peter; Qin, Lihui; Bielinska, Anna U . ; Kukowska-Latallo, Jolanta F . ; Baker, James R . ; Bromberg, Jonathan S . (2001). "Combination of Electroporation and DNA/Dendrimer Complexes Enhances Gene Transfer into Murine Cardiac Transplants." American Journal of Transplantation 1(4): 334-338. <http://hdl.handle.net/2027.42/74413>en_US
dc.identifier.issn1600-6135en_US
dc.identifier.issn1600-6143en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/74413
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12099377&dopt=citationen_US
dc.format.extent233782 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherMunksgaard International Publishersen_US
dc.publisherBlackwell Publishing Ltden_US
dc.rightsMunksgaard, 2001en_US
dc.subject.otherDendrimeren_US
dc.subject.otherElectroporation , Gene Transfer , Transplantationen_US
dc.titleCombination of Electroporation and DNA/Dendrimer Complexes Enhances Gene Transfer into Murine Cardiac Transplantsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCenter for Biologic Nanotechnology, The University of Michigan, Ann Arbor, MI 48105, USAen_US
dc.contributor.affiliationotherInstitute for Gene Therapy and Molecular Medicine and the Recanati/Miller Transplantation Institute, Mount Sinai School of Medicine, New York, NY 10029-6574, USAen_US
dc.identifier.pmid12099377en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/74413/1/j.1600-6143.2001.10408.x.pdf
dc.identifier.doi10.1034/j.1600-6143.2001.10408.xen_US
dc.identifier.sourceAmerican Journal of Transplantationen_US
dc.identifier.citedreferenceYinong Wang L, Qin Y, Bai AU et al. DNA/dendrimer complexes mediate gene transfer into murine cardiac transplants ex vivo. Mol Ther 2000; 2: 602 – 608.en_US
dc.identifier.citedreferenceQin L, Chavin KD, Ding Y et al. Multiple vectors effectively achieve gene transfer in a murine cardiac transplantation model: immunosuppression with TGF-β1 or vIL-10. Transplantation 1995; 59: 809 – 816.en_US
dc.identifier.citedreferenceAcsadi G, Jiao S, Jani A et al. Direct gene transfer and expression into rat heart in vivo. The New Biologist 1991; 3: 71 – 81.en_US
dc.identifier.citedreferenceLin H, Parmacek MS, Morle G, Bolling S, Leiden JM. Expression of recombinant genes in myocardium in vivo after direct injection of DNA. Circulation 1990; 82: 2217 – 2221.en_US
dc.identifier.citedreferenceStratford-Perricaudet LD, Makeh I, Perricaudet M, Briand P. Expression of recombinant genes in myocardium in vivo after direct injection of DNA. J Clin Invest 1992; 90: 626 – 630.en_US
dc.identifier.citedreferenceKass-Eisler A, Falck-Pedersen E, Alvira M et al. Quantitative determination of adenovirus-mediated gene delivery to rat cardiac myocytes in vitro and in vivo. Proc Natl Acad Sci USA 1993; 90: 11498 – 11502.en_US
dc.identifier.citedreferenceWang J, Ma Y, Knechtle SJ. Adenovirus-mediated gene transfer into rat cardiac allografts. Transplantation 1996; 61: 1726 – 1729.en_US
dc.identifier.citedreferenceDonahue JK, Kikkawa K, Johns DC, Marban E, Lawrence JH. Ultrarapid, highly efficient viral gene transfer to the heart. Proc Natl Acad Sci USA 1997; 94: 4664 – 4668.en_US
dc.identifier.citedreferenceSawa Y, Kaneda Y, Bai H-Z et al. Efficient transfer of oligonucleotides and plasmid DNA into the whole heart through the coronary artery. Gene Therapy 1998; 5: 1472 – 1480.en_US
dc.identifier.citedreferenceDonahue JK, Kikkawa K, Thomas AD, Marban E, Lawrence JH. Acceleration of widespread adenoviral gene transfer to intact rabbit hearts by coronary perfusion with low calcium and serotonin. Gene Therapy 1998; 5: 630 – 634.en_US
dc.identifier.citedreferenceMann MJ, Gibbons GH, Hutchinson H et al. Pressure-mediated oligonucleotide transfection of rat and human cardiovascular tissues. Proc Natl Acad Sci USA 1999; 96: 6411 – 6416.en_US
dc.identifier.citedreferenceFromes Y, Salmon A, Wang X et al. Gene delivery to the myocardium by intrapericardial injection. Gene Therapy 1999; 6: 683 – 688.en_US
dc.identifier.citedreferenceSvensson EC, Marshall DJ, Woodard K et al. Efficient and stable transduction of cardiomyocytes after intramyocardial injection or intracoronary perfusion with recombinant adeno-associated virus vectors. Circulation 1999; 99: 201 – 205.en_US
dc.identifier.citedreferencePalasis M, Luo Z, Barry JJ, Walsh K. Analysis of adenoviral transport mechanism in the vessel wall and optimization of gene transfer using local delivery catheters. Hum Gene Ther 2000; 11: 237 – 246.en_US
dc.identifier.citedreferenceNeumann E, Schaefer-Ridder M, Wang Y, Hofschneider PH. Gene transfer into mouse myeloma cells by electroporation in high electric fields. EMBO J 1982; 1: 841 – 845.en_US
dc.identifier.citedreferenceHeller R, Jaroszeski M, Atkin A et al. In vivo gene electroinjection and expression in rat liver. FEBS Lett 1996; 389: 225 – 228.en_US
dc.identifier.citedreferenceNishi T, Yoshizato K, Yamashiro S et al. High-efficiency in vivo gene transfer using intraarterial plasmid DNA injection following in vivo electroporation. Cancer Res 1996; 56: 1050 – 1055.en_US
dc.identifier.citedreferenceSuzuki T, Shin B, Fujikura K, Matsuzaki T, Takata K. Direct gene transfer into rat liver cells by in vivo electroporation. FEBS Lett 1998; 425: 436 – 440.en_US
dc.identifier.citedreferenceHarrison RL, Byrne BJ, Tung L. Electroporation-mediated gene transfer in cardiac tissue. FEBS Lett 1998; 435: 1 – 5.en_US
dc.identifier.citedreferenceGoto T, Nishi T, Tamura T et al. Highly efficient electro-gene therapy of solid tumor by using an expression plasmid for the herpes simplex virus thymidine kinase gene. Proc Natl Acad Sci USA 2000; 97: 354 – 359.en_US
dc.identifier.citedreferenceMaruyama H, Sugawa M, Moriguchi Y et al. Continuous erythropoietin delivery by muscle-targeted gene transfer using in vivo electroporation. Hum Gene Ther 2000; 11: 429 – 437.en_US
dc.identifier.citedreferenceWidera G, Austin M, Rabussay D et al. Increased DNA vaccine delivery and immunogenicity by electroporation in vivo. J Immunol 2000; 164: 4635 – 4640.en_US
dc.identifier.citedreferenceBettan M, Emmanuel F, Darteil R et al. High-level protein secretion into blood circulation after electric pulse-mediated gene transfer into skeletal muscle. Mol Ther 2000; 2: 204 – 210.en_US
dc.identifier.citedreferenceWells JM, Li LH, Sen A, Jahreis GP, Hui SW. Electroporation-enhanced gene delivery in mammary tumors. Gene Therapy 2000; 7: 541 – 547.en_US
dc.identifier.citedreferenceSomiari S, Glasspool-Malone J, Drabick JJ et al. Theory and in vivo application of electroporative gene delivery. Mol Ther 2000; 2: 178 – 187.en_US
dc.identifier.citedreferenceKukowska-Latallo JF, Bielinska AU, Johnson J, Spindler R, Tomalia DA, Baker JR. Efficient transfer of genetic material into mammalian cells using Starburst polyamidoamine dendrimers. Proc Natl Acad Sci USA 1996; 93: 4897 – 4902.en_US
dc.identifier.citedreferenceKukowska-Latallo JF, Chen C, Eichman J, Bielinska AU, Baker JR Jr. Enhancement of dendrimer-mediated transfection using synthetic lung surfactant exosurf neonatal in vitro. Biochem Biophys Res Commun 1999; 264: 253 – 261.en_US
dc.identifier.citedreferenceRaczka E, Kukowska-Latallo JF, Rymaszewski M, Chen C, Baker JR Jr. The effect of synthetic surfactant exosurf on gene transfer in mouse lung in vivo. Gene Therapy 1998; 5: 1333 – 1339.en_US
dc.identifier.citedreferenceQin L, Pahud DR, Ding Y et al. Efficient transfer of genes into murine cardiac grafts by Starburst polyamidoamine dendrimers. Hum Gene Ther 1998; 9: 553 – 560.en_US
dc.identifier.citedreferenceGuillot C, Mathieu P, Coathalem H et al. Tolerance to cardiac allografts via local and systemic mechanisms after adenovirus-mediated CTLA1Ig expression. J Immunol 2000; 164: 5258 – 5268.en_US
dc.identifier.citedreferenceSuzuki J, Morishita R, Amano J, Kaneda Y, Isobe M. Decoy against nuclear factor-kappa B attenuates myocardial cell infiltration and arterial neointimal formation in murine cardiac allografts. Gene Therapy 2000; 7: 1847 – 1852.en_US
dc.identifier.citedreferenceKawauchi M, Suzuki J, Morishita R et al. Gene therapy for attenuating cardiac allograft arteriopathy using ex vivo E2F decoy transfection by HVJ-AVE-liposome method in mice and nonhuman primates. Circ Res 2000; 87: 1063 – 1068.en_US
dc.identifier.citedreferenceChan SY, Goodman RE, Szmuszkovicz JR, Roessler B, Eichwald EJ, Bishop DK. DNA-liposome versus adenoviral mediated gene transfer of transforming growth factor β1 in vascularized cardiac allografts: differential sensitivity of CD4+ and CD8+ T cells to transforming growth factorβ1. Transplantation 2000; 70: 1292 – 1301.en_US
dc.identifier.citedreferenceFlotte T, Agarwal A, Wang J et al. Efficient ex vivo transduction of pancreatic islet cells with recombinant adeno-associated virus vectors. Diabetes 2001; 50: 515 – 520.en_US
dc.identifier.citedreferenceTakehara M, Murakami M, Inobe M et al. Long-term acceptance of allografts by in vivo gene transfer of regulatable adenovirus vector containing CTLA4IgG and lox P. Hum Gene Ther 2001; 12: 415 – 426.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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