Stem Cell Center
Stem cells are unique in their capacity to proliferate and replacing cells – often life-long. However, many adult organs, such as the brain or the pancreas, have no or few stem cells. The Department’s mission builds on our pioneer approach to reprogram local cells towards the lost cell type identity in such organs and on our pioneer discoveries on epigenetic mechanisms of reprogramming. The key proteins that enable such fate conversion have been all identified for their role during development, when all relevant cell types are generated. Our Department therefore combines in a world-wide unique combination expertise in stem cells, developmental mechanisms of fate specification and plasticity including a strong epigenetic expertise with injury models and direct reprogramming.
Stem Cell Center
Replacing lost or damaged cells is the cornerstone of regenerative medicine. To achieve this, we need to understand not only how cells acquire their specific identity but also how cell plasticity is regulated. Helmholtz Munich’s Stem Cell Center is unique worldwide in combining leading expertise in cell plasticity, epigenetics, and direct reprogramming.
Recent Publications
See all2024 Nat Neurosci. 2024 Jul 2.
2024 Cell Discovery volume 10, Article number: 42 (2024)
Engineered, nucleocytoplasmic shuttling Cas13d enables highly efficient cytosolic RNA targeting
2024 Neuron P1117-1132.e9, April 03, 2024
2024 Nature Communication 15(1):2866
2024 Nature 625, pages 401–409 (2024)
Emergence of replication timing during early mammalian development
2023 Nature Medicine 29, 3149-3161
Injury-specific factors in the cerebrospinal fluid regulate astrocyte plasticity in the human brain
2023 Nature Communications 14, Article number: 7674 (2023)
A reversible state of hypometabolism in a human cellular model of sporadic Parkinson’s disease
2023 Mol Cancer. 2023 Jul 8;22(1)
Combined proteomics and CRISPR‒Cas9 screens in PDX identify ADAM10 as essential for leukemia in vivo
2023 Blood. 2023 Feb 23;141(8):955-960
WT1 and DNMT3A play essential roles in the growth of certain patient AML cells in mice