One of the effective ways to explore development is through the use of stem cell-derived cell types. However, these models still face challenges in terms of maturity, reproducibility, and accurately representing various cell types. Our objective is to address these limitations by building new models or improvising existing ones, with a particular emphasis on comprehending the role of supporting cells in the development and functionality of stem cell models. Through the application of advanced imaging techniques, organoid systems, and molecular profiling methods, this study aims to unravel the signaling pathways, paracrine factors, and physical interactions that occur between these cell types.
Stem cells have the potential to revolutionize regenerative medicine by serving as a key component in the development of cell-free therapeutic products. In order to explore this potential, our research aims to create pipelines for the advancement of cell-free systems specifically designed for therapeutic applications.
The process of determining a cell's fate is a complex phenomenon that entails intricate interactions among genetic factors, epigenetic modifications, and changes in genome organization. Our focus lies in comprehending the significance of chromatin regulators in governing cell fate decisions related to reprogramming, pluripotency, and differentiation. By studying these regulators, we aim to gain insights into the mechanisms underlying cellular identity and the potential for manipulating cell fate for various biomedical applications.
Our current focus is to gain a comprehensive understanding of metabolic and rare genetic disorders by utilizing stem cell-derived organoids. Through the integration of genome editing techniques and collaborations with clinical experts, our objective is to unravel the specific contributions of various gene variants to the progression of these diseases.