dc.contributor.advisor | Vonka, Vladimír | |
dc.creator | Lakatošová, Monika | |
dc.date.accessioned | 2019-05-03T16:44:10Z | |
dc.date.available | 2019-05-03T16:44:10Z | |
dc.date.issued | 2011 | |
dc.identifier.uri | http://hdl.handle.net/20.500.11956/35290 | |
dc.description.abstract | Genesfor two cytokines,one chemokineandgenecoding for oneangiostaticfactor were used in the presentwork for tansfection ofmouse IIPV-16- transformedtumor cells. Main characteristics oftransduced cells werc t€stedrnraTo and,in vivo and,cnrnparedwith theparentaltumor cells. In the first part I useda thymidine-kinase deficient (cTK) cell line designated123IA, which had beenderived from IIPVI6 transformedmouse(C57BL/6) cells MK16. To obain genetically modified cells, 1231Acells were transfectedwith bicistronic plasmids carrying the herpessimplex type 1thymidine kinase(HSV-TK) gen,eandeitherthe genefor the mouseB7-l (CD80) co-stimulatory molecule or the gene for the monocyte-chemoattractantprotsin 1 (MCP-|). For control putposes,a plasmid vector carrying only the HSV-TK genewas used.For comparativepurposesI also used89 cells, previously isolated in our laboratory, which expressthe mousegranulocyte-macrophagecolony stimulation factor (GM-CSF) andHSV-TK gene.All the cell lines testedwere found to be sensitiveto minute amountsof ganciclovir, revealing the production of functional HSV-TK. When inoculatedinto syngeneic mice, cells expressing either GM-CSF or B7-1 were non-oncogenic. Nearly all mice inoculatedwith MCP-l-producingcellsdevelopedtumors.Animalsinjectedwith GM-CSF or B7-l- producing cells were... | en_US |
dc.description.abstract | Souhrn Vt6toprAcijsemzkoumalavlastnostimy3lchbun6ktransformovanfchviremHPV16'kfer6 byly genetickymodifikovfny vnesenimgent pro cytokiny' chemokin ajeden angiostaticki gen' Byly testovAnyhlavnlcharakteristikytransdukovanfchbun€kvporovnAnisrodidovkjminddorovfmi buikami in vitro a in viYo VprvnldristijsempouZilabunddnouliniidefrcientnlnabunddnoutymidinkin6zu'ozratenou jakol23IA,kter6bylaodvozenazmy5ich(c57BLl6)ledvinnjchbun€ktransformovarrjchonkogeny E6lETHPV16aaktivovanfmonkogenemH.rasomaEenlchjakoMK16.Builkyl23IAjsem transfekovala bicistronickfmi plazmidy nesoucimi geny pro herpetickou tymidin kin6zu (HSv-Tn, kostimulaini molekulu B7-,1(cD 80) nebochemokin - protein 1 chemoatrahujicimonocyty (MCP-L)' ho kontrolni idely jsem pouZilaplazmid obsahujicljen genpro I/SY-IK' Do testfijsem zahrnulatak€ diive izolovan6 bufiky Bg, kterd byly transdukov6ny geny pro faktor stimulujicl tvorbu kolonii granulocytiamonocytft(GM-cSnaHSV-TK'VSechnyizolovan6liniebylycitliv6kegancikloviru' prokazujice tak piitomnost HSV-TK. po inokulaci syngennimmystm, byly bunky exprimujici GM- CSFa B7-l neonkogenni.Po odkov6nibunEkprodukujicichMCP-I vfvofily t6m6l v5echnymy3i fl(dory. Zvl?rltaimtmizovani bunkami produkujici GM-CSF a B7-l byla chr6ndnapled n6slednou... | cs_CZ |
dc.language | Čeština | cs_CZ |
dc.language.iso | cs_CZ | |
dc.publisher | Univerzita Karlova, Přírodovědecká fakulta | cs_CZ |
dc.title | Vlastnosti myších buněk, které byly modifikovány geny pro imunomodulační faktory a endostatin | cs_CZ |
dc.type | dizertační práce | cs_CZ |
dcterms.created | 2011 | |
dcterms.dateAccepted | 2011-06-16 | |
dc.description.department | Department of Genetics and Microbiology | en_US |
dc.description.department | Katedra genetiky a mikrobiologie | cs_CZ |
dc.description.faculty | Faculty of Science | en_US |
dc.description.faculty | Přírodovědecká fakulta | cs_CZ |
dc.identifier.repId | 108441 | |
dc.title.translated | Characteristics of HPV16 transformed mice cells, transduced with genes for immunomodulating factors and endostatin | en_US |
dc.contributor.referee | Reiniš, Milan | |
dc.contributor.referee | Forstová, Jitka | |
dc.identifier.aleph | 001394852 | |
thesis.degree.name | Ph.D. | |
thesis.degree.level | doktorské | cs_CZ |
thesis.degree.discipline | - | cs_CZ |
thesis.degree.discipline | - | en_US |
thesis.degree.program | Molekulární a buněčná biologie, genetika a virologie | cs_CZ |
thesis.degree.program | Molecular and Cell Biology, Genetics and Virology | en_US |
uk.thesis.type | dizertační práce | cs_CZ |
uk.taxonomy.organization-cs | Přírodovědecká fakulta::Katedra genetiky a mikrobiologie | cs_CZ |
uk.taxonomy.organization-en | Faculty of Science::Department of Genetics and Microbiology | en_US |
uk.faculty-name.cs | Přírodovědecká fakulta | cs_CZ |
uk.faculty-name.en | Faculty of Science | en_US |
uk.faculty-abbr.cs | PřF | cs_CZ |
uk.degree-discipline.cs | - | cs_CZ |
uk.degree-discipline.en | - | en_US |
uk.degree-program.cs | Molekulární a buněčná biologie, genetika a virologie | cs_CZ |
uk.degree-program.en | Molecular and Cell Biology, Genetics and Virology | en_US |
thesis.grade.cs | Prospěl/a | cs_CZ |
thesis.grade.en | Pass | en_US |
uk.abstract.cs | Souhrn Vt6toprAcijsemzkoumalavlastnostimy3lchbun6ktransformovanfchviremHPV16'kfer6 byly genetickymodifikovfny vnesenimgent pro cytokiny' chemokin ajeden angiostaticki gen' Byly testovAnyhlavnlcharakteristikytransdukovanfchbun€kvporovnAnisrodidovkjminddorovfmi buikami in vitro a in viYo VprvnldristijsempouZilabunddnouliniidefrcientnlnabunddnoutymidinkin6zu'ozratenou jakol23IA,kter6bylaodvozenazmy5ich(c57BLl6)ledvinnjchbun€ktransformovarrjchonkogeny E6lETHPV16aaktivovanfmonkogenemH.rasomaEenlchjakoMK16.Builkyl23IAjsem transfekovala bicistronickfmi plazmidy nesoucimi geny pro herpetickou tymidin kin6zu (HSv-Tn, kostimulaini molekulu B7-,1(cD 80) nebochemokin - protein 1 chemoatrahujicimonocyty (MCP-L)' ho kontrolni idely jsem pouZilaplazmid obsahujicljen genpro I/SY-IK' Do testfijsem zahrnulatak€ diive izolovan6 bufiky Bg, kterd byly transdukov6ny geny pro faktor stimulujicl tvorbu kolonii granulocytiamonocytft(GM-cSnaHSV-TK'VSechnyizolovan6liniebylycitliv6kegancikloviru' prokazujice tak piitomnost HSV-TK. po inokulaci syngennimmystm, byly bunky exprimujici GM- CSFa B7-l neonkogenni.Po odkov6nibunEkprodukujicichMCP-I vfvofily t6m6l v5echnymy3i fl(dory. Zvl?rltaimtmizovani bunkami produkujici GM-CSF a B7-l byla chr6ndnapled n6slednou... | cs_CZ |
uk.abstract.en | Genesfor two cytokines,one chemokineandgenecoding for oneangiostaticfactor were used in the presentwork for tansfection ofmouse IIPV-16- transformedtumor cells. Main characteristics oftransduced cells werc t€stedrnraTo and,in vivo and,cnrnparedwith theparentaltumor cells. In the first part I useda thymidine-kinase deficient (cTK) cell line designated123IA, which had beenderived from IIPVI6 transformedmouse(C57BL/6) cells MK16. To obain genetically modified cells, 1231Acells were transfectedwith bicistronic plasmids carrying the herpessimplex type 1thymidine kinase(HSV-TK) gen,eandeitherthe genefor the mouseB7-l (CD80) co-stimulatory molecule or the gene for the monocyte-chemoattractantprotsin 1 (MCP-|). For control putposes,a plasmid vector carrying only the HSV-TK genewas used.For comparativepurposesI also used89 cells, previously isolated in our laboratory, which expressthe mousegranulocyte-macrophagecolony stimulation factor (GM-CSF) andHSV-TK gene.All the cell lines testedwere found to be sensitiveto minute amountsof ganciclovir, revealing the production of functional HSV-TK. When inoculatedinto syngeneic mice, cells expressing either GM-CSF or B7-1 were non-oncogenic. Nearly all mice inoculatedwith MCP-l-producingcellsdevelopedtumors.Animalsinjectedwith GM-CSF or B7-l- producing cells were... | en_US |
uk.file-availability | V | |
uk.publication.place | Praha | cs_CZ |
uk.grantor | Univerzita Karlova, Přírodovědecká fakulta, Katedra genetiky a mikrobiologie | cs_CZ |
thesis.grade.code | P | |
dc.identifier.lisID | 990013948520106986 | |