Prof Thomas Iskratsch
Dipl.-Ing. (Equiv. to MSc/MEng), PhD
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Current Funded Research Projects
Start: 01-09-2023 / End: 31-08-2026
Start: 01-12-2020 / End: 30-11-2023
Vascular smooth muscle cellsplay a central role in the onset and progression of many cardiovascular diseases, from atherosclerosis to vascular injury, where their migration, matrix secretion, or degradation functions are deregulated. Here we are investigating how the phenotypic switch is regulated through physical/mechanical stimuli.
Current PhD Studentship Projects
Virtual Atria with Personalised Electrophysiology for Atrial Fibrillation Therapy Planning - SEMS Industry-supported PhD StudentshipFunding source: Acutus Medical UK Ltd
Start: 01-10-2022 / End: 30-09-2025
Start: 04-10-2021 / End: 03-10-2024
Development of functional 3D eccrine sweat gland model
Start: 01-07-2021 / End: 30-06-2024
Previous Funded Research Projects
Start: 04-01-2021 / End: 30-04-2023
The project aims to develop a photoelectrochemical imaging system for mapping of electrochemical processes in three dimensions within porous electrode structures. The new technology will aid the development of novel electrode materials for energy harvesting devices and be suitable for in-situ 3D functional imaging in 3D tissue culture.
Investigating the cardiomyocyte rigidity sensing mechanism with micro patterned surfaces and nanopil
Start: 01-02-2019 / End: 31-03-2023
The composition and the stiffness of the cardiac extracellular matrix change during development or in heart disease. Cardiomyocytes and their progenitors sense these changes, which decides over Cardiomyocyte fate. Our preliminary data suggested a cardiomyocyte specific rigidity sensing mechanism which we will investigate here in detail.
Start: 01-01-2015 / End: 31-12-2018
While chemical cues have well-established roles in guiding cell differentiation, there is growing evidence of a role for mechanical stimuli, such as matrix rigidity during heart development and disease. However, the mechanisms that underlie this mechanical signalling remain elusive. Here we will study this by combining cell biology, biophysics and nanotechnology in a three-tiered approach in which we examine the cardiomyocyte response to A) passive resistance and varying rigidity; B) active force; C) no force. Detailed understanding will lead to novel and valuable insights into mechanisms of cardiac mechanosensing and could result in novel or improved therapeutic strategies for cardiac diseases.