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The role of indolamine 2,3 deoxygenase in the immunomodulation of ulcerative colitis: parameters of inflammation in the oral cavity and colon

dc.contributor.advisorVolarević, Vladislav
dc.contributor.otherRistić, Vladimir
dc.contributor.otherVojvodić, Danilo
dc.contributor.otherMilovanović, Jelena
dc.contributor.otherSimović-Marković, Bojana
dc.creatorAcović, Aleksandar
dc.date.accessioned2020-12-30T12:24:43Z
dc.date.available2020-12-30T12:24:43Z
dc.date.issued2020-09-17
dc.identifier.urihttp://eteze.kg.ac.rs/application/showtheses?thesesId=7758
dc.identifier.urihttps://fedorakg.kg.ac.rs/fedora/get/o:1288/bdef:Content/download
dc.identifier.urihttps://nardus.mpn.gov.rs/handle/123456789/17751
dc.descriptionUlcerozni kolitis je inflamacijska bolest creva koja se karakteriše fazama egzacerbacije i remisije. Zbog sličnosti u pogledu molekulskih mehanizama odgovornih za nastanak i progresiju, mišji kolitis indukovan dekstran natrijum sulfatom (DSS-kolitis) je jedan od najčešće korišćenih eksperimentalnih modela za ispitivanje ulceroznog kolitisa. Analogno ulceroznom kolitisu ljudi, imunske ćelije (makrofagi, dendritske ćelije (DCs), neutrofili, T limfociti) imaju najvažniju ulogu u patogenezi DSS-kolitisa. Regulatorni T limfociti (Treg), produkcijom imunosupresivnih citokina, suprimiraju inflamaciju i podstiču regeneraciju oštećene sluznice creva. Postoji dramatična razlika u toku DSS-kolitisa kod miševa različitih sojeva. Tako, BALBc miševi razvijaju lakši oblik bolesti sa spontanom regeneracijom sluzokože creva dok S57BL/6 miševi razvijaju težu formu bolesti koja progredira u hronicitet. U lamina propri-ji creva se triptofan metaboliše kinureninskim putem, aktivnošću enzima indolamin 2,3 dioksigenaze (IDO). Najveća aktivnost IDO-a je zabeležena u DCs i mezenhimskim matičnim ćelijama (MSCs) koje se zbog svojih imunomodulacijskih karakteristika primenjuju u terapiji inflamacijskih bolesti, uključujući i ulcerozni kolitis. Rezultati ove studije su pokazali da DCs BALBc miševa poseduju znatno veći kapacitet produkcije IDO-a naspram DCs C57BL/6 životinja, što sledstveno indukuje ekspanziju Treg limfocita koji suprimiraju inflamaciju i podstiču regeneraciju sluznice creva. Stepen oštećenja sluznice creva, pa tako i razvoj bolesti, se najpouzdanije utvrđuju kolonoskopijom, ali se ova invazivna dijagnostička metoda ne može često izvoditi. Određivanje fekalnog kalprotektina predstavlja najčešće korišćeni alternativni dijagnostički parametar za praćenje toka bolesti i uspešnosti terapije. Ipak, nedostatak validiranog cut-off-a i nedovoljna specifičnost ovog testa, ukazuje na potrebu za uvođenje novih neinvazivnih dijagnostičkih metoda kojim se može procenjivati uspešnost terapije i stepen regeneracije obolele sluznice. Rezultati ove studije ukazuju da se praćenjem koncentracije kinurenina u gingivalnoj tečnosti, serumu i fecesu može pratiti progresija ulceroznog kolitisa. Zbog činjenice da su MSCs jedan od najznačajnih izvora IDO-a, u ovoj studiji je ispitivan i značaj IDO/kinureninskog puta za terapijske efekte MSCs u imunomodulaciji DSS-kolitisa. Koncentracija inflamacijskih citokina, posebno 4 IFN-γ i TNF-α, utiču na promenu fenotipa i efektorskih funckija MSCs. MSCs su nakon aplikacije u miševe soja C57BL/6 (u kojima je serumska koncentracija inflamacijskih citokina bila visoka), uzrokovale značajan porast koncentracije kinurenina u serumu što je rezultiralo ekspanzijom Treg limfocita u crevima, smanjenjem inflamacije i ublažavanjem simptoma kolitisa. Sa druge strane, nakon aplikacije u DSS-om tretirane BALBc miševe (kod kojih su bile niske vrednosti inflamacijskih citokina), MSCs nisu uzrokovale IDO/kinurenin-zavisnu ekspanziju Treg limfocita u crevima već su indukovale ekspanziju inflamacijskih ćelija u kolonu što je dovelo do pogoršanja kolitisa.sr
dc.descriptionUlcerative colitis is an entity of inflammatory bowel disease characterized by stages of exacerbation and remission. Due to the similarity with respect to the molecular mechanisms responsible for the onset and progression, murine colitis induced by dextran sodium sulfate (DSS-colitis) is one of the most commonly used experimental models for testing ulcerative colitis. Analogous to human ulcerative colitis, immune cells (macrophages, dendritic cells (DCs), neutrophils, T lymphocytes) play the most important role in the pathogenesis of DSScolitis. Regulatory T lymphocytes (Tregs), by producing immunosuppressive cytokines, suppress inflammation and promote the regeneration of damaged intestinal mucosa. There is a striking difference in the course of DSS-colitis in mice of different strains. Thus, BALBc mice develop a milder form of disease with spontaneous regeneration of intestinal mucosa while C57BL/6 mice develop a more severe form of disease that progresses to chronicity. In the lamina propria of the intestine, tryptophan is been metabolized by kynurenine via the activity of the enzyme indoleamine 2,3 dioxygenase (IDO). The highest activity of IDOs has been reported in DCs and mesenchymal stem cells (MSCs), which, because of their immunomodulatory properties, are used in the treatment of inflammatory diseases, including ulcerative colitis. The results of this study showed that DCs of BALBc mice have a significantly higher IDO production capacity than DCs of C57BL/6 animals, which consequently induces the expansion of Treg cells that suppress inflammation and promote mucosal regeneration. The degree of damage to the intestinal mucosa, as well as the development of the disease, are most reliably determined by colonoscopy, but this invasive diagnostic method cannot be performed frequently. The determination of fecal calprotectin is the most commonly used alternative diagnostic parameter for monitoring the course of the disease and the success of therapy. However, the lack of validated cut-off and the lack of specificity of this test indicate the need for the introduction of new, non-invasive diagnostic methods that can evaluate the success of therapy and the degree of regeneration of diseased mucosa. Our results indicate that the monitoring of local and systemic parameters of ulcerative colitis can be observed by monitoring the concentrations of immunomodulatory factors in gingival fluid, serum and feces. MSCs have been used in the treatment of ulcerative colitis for their immunomodulatory properties, but the results are bidirectional. As one of the most significant sources of IDO, we examined the role of IDO/kynurenine pathway in immunomodulation of mesenchymal stem cells in a model of DSS-induced colitis. After application of MSCs in C57BL/6 strain mice, 6 they polarized the immune response and transferred the medium from proinflammatory to immunosuppressive environment, where Treg lymphocyte expansion suppressed inflammation and allowed regeneration. On the other hand, the application of MSCs in animals of the BALBc strain contributed to the overall exacerbation of the disease followed by an increase in inflammation parameters.en
dc.formatapplication/pdf
dc.languagesr
dc.publisherУниверзитет у Крагујевцу, Факултет медицинских наукаsr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/41008/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/173056/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/175069/RS//
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/175103/RS//
dc.rightsopenAccessen
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceУниверзитет у Крагујевцуsr
dc.subjectindoleamine 2,3-dioxygenasesr
dc.subjectindoleamine 2,3-dioxygenaseen
dc.subjectkynureninesr
dc.subjectdextran sodium sulphateinduced colitissr
dc.subjectC57BL/6 micesr
dc.subjectBALB/c micesr
dc.subjectmesenchymal stem cellssr
dc.subjectulcerative colitissr
dc.subjectkynurenineen
dc.subjectdextran sodium sulphateinduced colitisen
dc.subjectC57BL/6 miceen
dc.subjectBALB/c miceen
dc.subjectmesenchymal stem cellsen
dc.subjectulcerative colitisen
dc.titleUloga indolamin 2,3 deoksigenaze u imunomodulaciji ulceroznog kolitisa: parametri inflamacije u usnoj duplji i kolonusr
dc.title.alternativeThe role of indolamine 2,3 deoxygenase in the immunomodulation of ulcerative colitis: parameters of inflammation in the oral cavity and colonen
dc.typedoctoralThesisen
dc.rights.licenseBY-NC-ND
dcterms.abstractВоларевић, Владислав; Војводић, Данило; Миловановић, Јелена; Симовић-Марковић, Бојана; Ристић, Владимир; Aцовић, Aлександар; Улога индоламин 2,3 деоксигеназе у имуномодулацији улцерозног колитиса: параметри инфламације у усној дупљи и колону; Улога индоламин 2,3 деоксигеназе у имуномодулацији улцерозног колитиса: параметри инфламације у усној дупљи и колону;
dc.identifier.fulltexthttps://nardus.mpn.gov.rs/bitstream/id/67650/Aleksandar_Acovic_Medicina.pdf
dc.identifier.fulltexthttps://nardus.mpn.gov.rs/bitstream/id/67649/Disertacija.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_nardus_17751


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