Institute for Regenerative Medicine
I am currently working as a Group Leader at the Institute for Regenerative Medicine of the University of Zurich, Switzerland and focus on basic and translational research in vascular and neurobiology. I received my PhD at the ETH Zurich, Switzerland in 2019 defending the thesis entitled “Vascular Repair after Ischemia” supervised by Prof. Dr. M.E. Schwab. During the PhD, I became interested in translational stroke research and developing regenerative therapies in preclinical rodent models. From 2019, I joined the group of Prof. Dr. R.M. Nitsch and Dr. C. Tackenberg in the Institute for Regenerative Medicine (IREM) at the University of Zurich, Switzerland. In this project, I focused on developing next-generation stem cell-based therapies following stroke. I am currently member of the Society for Neuroscience (SFN) and European Society for Clinical Investigation (ESCI). I received several fellowships and awards including the selection as a Young Scientist for the 70th Lindau Nobel Laureate Meeting 2020 by the Lindau Nobel committee and a full doctoral fellowship by the German Academic Scholarship Foundation, Germany’s largest and most prestigious scholarship foundation. Our current research focuses on overcoming limitations in cell therapies following brain injury using state-of-the-art genetic, molecular, and computational tools. We have recently generated a scalable neural cell source from induced pluripotent stem cells (iPSCs) under xeno-free conditions that can be continuously tracked in vivo. These cells will be genetically engineered with a brain-shuttle system to facilitate systemic delivery across the brain barriers. To circumvent immune rejection, transplants will co-express distinct immunosuppressive molecules together with safety checkpoints. Efficacy of these advanced cell therapies will be evaluated through an experimental pipeline comprising i.a. in vivo imaging, deep learning-based behavioral profiling, and spatially resolved transcriptomics. The generated findings will be valuable to advance cell therapy for brain injury further towards clinical applications in the foreseeable future.
Mast cells increase adult neural precursor proliferation and differentiation but this potential is not realized in vivo under physiological conditions.
Scientific reports 12, 2017 | Pubmed ID: 29259265
Stroke Promotes Systemic Endothelial Inflammation and Atherosclerosis.
Trends in molecular medicine 07, 2018 | Pubmed ID: 29747910
Loss of Nogo-A, encoded by the schizophrenia risk gene Rtn4, reduces mGlu3 expression and causes hyperexcitability in hippocampal CA3 circuits.
PloS one , 2018 | Pubmed ID: 30040841
Pro- and antiangiogenic therapies: current status and clinical implications.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 01, 2019 | Pubmed ID: 30085886
Inflammation after Stroke: A Local Rather Than Systemic Response?
Trends in neurosciences 12, 2018 | Pubmed ID: 30327142
A Revised View on Growth and Remodeling in the Retinal Vasculature.
Scientific reports 03, 2019 | Pubmed ID: 30824785
Nogo-A targeted therapy promotes vascular repair and functional recovery following stroke.
Proceedings of the National Academy of Sciences of the United States of America 07, 2019 | Pubmed ID: 31235580
Refueling the Ischemic CNS: Guidance Molecules for Vascular Repair.
Trends in neurosciences 09, 2019 | Pubmed ID: 31285047
Anti-Nogo-A antibodies prevent vascular leakage and act as pro-angiogenic factors following stroke.
Scientific reports 12, 2019 | Pubmed ID: 31882970
Insights into the dual role of angiogenesis following stroke.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 06, 2020 | Pubmed ID: 32065073
A Practical Guide to the Automated Analysis of Vascular Growth, Maturation and Injury in the Brain.
Frontiers in neuroscience , 2020 | Pubmed ID: 32265643
Distinct changes in all major components of the neurovascular unit across different neuropathological stages of Alzheimer's disease.
Brain pathology (Zurich, Switzerland) 11, 2020 | Pubmed ID: 32866303
Author Correction: Mast cells increase adult neural precursor proliferation and differentiation but this potential is not realized in vivo under physiological conditions.
Scientific reports Nov, 2020 | Pubmed ID: 33168937
Characterization of the Blood Brain Barrier Disruption in the Photothrombotic Stroke Model.
Frontiers in physiology , 2020 | Pubmed ID: 33262704
Towards blood biomarkers for stroke patients.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 04, 2021 | Pubmed ID: 33563080
iPS-derived pericytes for neurovascular regeneration.
European journal of clinical investigation 09, 2021 | Pubmed ID: 34050924
Astrocytes for brain repair: More than just a neuron's sidekick.
Brain pathology (Zurich, Switzerland) 09, 2021 | Pubmed ID: 34196052
Isolation and Culture of Adult Hippocampal Precursor Cells as Free-Floating Neurospheres.
Methods in molecular biology (Clifton, N.J.) , 2022 | Pubmed ID: 34557999
'Scary' pericytes: the fibrotic scar in brain and spinal cord lesions.
Trends in neurosciences Jan, 2022 | Pubmed ID: 34774344
Slow development of bladder malfunction parallels spinal cord fiber sprouting and interneurons' loss after spinal cord transection.
Experimental neurology 02, 2022 | Pubmed ID: 34826427
APOE2, E3, and E4 differentially modulate cellular homeostasis, cholesterol metabolism, and inflammatory response in isogenic iPSC-derived astrocytes.
Stem cell reports Jan, 2022 | Pubmed ID: 34919811
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