Thesis, COLLÉGIALITÉ
Stepniak, Marty
Promotor(s) : Volders, Paul
Date of defense : 5-Jul-2022 • Permalink : http://hdl.handle.net/2268.2/14846
Details
Title : | Thesis, COLLÉGIALITÉ |
Translated title : | [en] Generation of hiPSC lines by PBMCs reprogramming and differentiation into contractile cardiomyocytes. |
Author : | Stepniak, Marty |
Date of defense : | 5-Jul-2022 |
Advisor(s) : | Volders, Paul |
Committee's member(s) : | Cataldo, Didier
Detry, Olivier Quesada Calvo, Florence |
Language : | French |
Number of pages : | 72 |
Keywords : | [fr] cellules souches / cardiomyocytes / hiPSC/ Maastricht University / Uliege/ culture cellulaire |
Discipline(s) : | Human health sciences > Laboratory medicine & medical technology |
Funders : | Maastricht University / Uliège |
Research unit : | CARIM center / Maastricht University |
Name of the research project : | Stem cell reprogramming and induced cardiomyocytes. |
Target public : | Researchers Professionals of domain Student |
Institution(s) : | Université de Liège, Liège, Belgique |
Degree: | Master en sciences biomédicales, à finalité approfondie |
Faculty: | Master thesis of the Faculté de Médecine |
Abstract
[en] Stem cells have for all time, and in the general consciousness, held out the promise of cell
regeneration, treatment of genetic diseases, grafts of new functional tissues, etc. A global
solution to very diverse pathologies, as the potential of these cells seems unlimited.
Today, these very special cells have indeed allowed significant advances in clinical and
translational medicine, on a small scale. It is therefore fundamental research that has finally
been able to take advantage of the almost unlimited differentiation potential of these cells,
making it possible to characterize pathological or cellular processes that were previously
unanswered, while waiting for a new model.
In this context, this thesis will focus on the reprogramming of somatic blood cells from patients
into induced pluripotent stem cells (hiPSC) and their differentiation into cardiac contractile
cells.
The objectives are multiple: The development and optimization of a protocol for the
reprogramming of blood cells into pluripotent cells and their subsequent differentiation into
cardiomyocytes. The characterization of cells at key stages of their development: from stem
cells to cardiomyocytes. And finally, in the short term, the electrophysiological analysis of the
induced cardiomyocytes to characterize the impact of specific inherited genetic mutations
carried by patients with a ventricular arrhythmia phenotype.
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