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040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aM.Sc
099 _aCai01.11.03.M.Sc.2018.Ma.E
100 0 _aManar Monir Youssef Amin
245 1 4 _aThe effect of mesenchymal stem cells derived microvesicles on the treatment of experimental CCL₄ induced liver fibrosis in rats /
_cManar Monir Youssef Amin ; Supervised Dina Sabry Abdelfatah , Abbas Mohamed Abbas , Heba Abdelmonem Ibrahim
246 1 5 _aتأثير الحويصلات الدقيقة المستخلصة من الخلايا الجذعية الميشنزمية على علاج التليف الكبدى الناجم عن حقن رباعى كلوريد الكربون فى فئران التجارب
260 _aCairo :
_bManar Monir Youssef Amin ,
_c2018
300 _a118 P. :
_bcharts , facsimiles ;
_c25cm
502 _aThesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Medical Biochemistry
520 _aBackground &Aim:Stem cell-based therapies especially the mesenchymal stem cells (MSCs) have potential for treatment of liver injury by contributing to regenerative responses, through functional tissue replacement or paracrine effects. The release of microvesicles (MVs) from these cells has been implicated in intercellular communication, and may contribute to beneficial paracrine effects of stem cell-based therapies. The aim of our study is to investigate the effect of administration of murine bone marrowMSC-MVs(mBM-MSC-MVs) on the treatment of carbon tetrachloride (CCL₄) induced liver fibrosis in rats.Thereby, to determine their potential utility as therapeutic agents for tissue repair and functional restoration in liver fibrosis. Methods : Our work included: Preparation, isolation then identification of BM-MSCs in culture by morphology and flow cytometry, preparation then identification of BM-MSC-MVs by transmission electron microscopy and polymerase chain reaction (PCR) detection of Ý-integrin gene expression, then preparation of rat model of liver fibrosis by CCl4-induced injury, injection of prepared BM-MSC-MVs in injured rats then the effects of BM-MSC-MVs were evaluated by biochemical analysis of liver functions, RNA gene expression quantitation for collagen-1Ü, transforming growth factor Ý(TGF-Ý), interleukin-1Ý(IL-1Ý), vascular endothelial growth factor (VEGF) by real time reverse transcription PCR (RT-PCR) techniquesand finally histopathologicalanalysis of the liver tissues of all studied groups
530 _aIssued also as CD
653 4 _aLiver fibrosis
653 4 _aMesenchymal stem cells
653 4 _aMicrovesicles
700 0 _aAbbas Mohamed Abbas ,
_eSupervisor
700 0 _aDina Sabry Abdelfatah ,
_eSupervisor
700 0 _aHeba Abdelmonem Ibrahim ,
_eSupervisor
856 _uhttp://172.23.153.220/th.pdf
905 _aNazla
_eRevisor
905 _aShimaa
_eCataloger
942 _2ddc
_cTH
999 _c67588
_d67588