Isabelle Mansuy
Neuroscientist
- 2 min read
- 2 chapters
Explore on Lably
ToursExplore Lably’s 3D toursEducation and career
Mansuy studied molecular biology and biotechnology at the University Louis Pasteur and the École Supérieure de Biotechnologie de Strasbourg. Mansuy went on to earn a PhD at the Friedrich Miescher Institute in Basel then a postdoc at Columbia University, where she gained expertise in neurobiology and in the design and use of transgenic mouse models. She established a lab as assistant professor at ETH Zürich at the end of 1998 and a few years later became professor in neuroepigenetics at the University of Zürich and ETH Zürich.
Sign in to keep reading
One more chapter is free with a Lably account.
Research
Mansuy initially worked on the molecular mechanisms of memory using mouse models. Her team revealed the specific molecules that allow the adult brain to forget through constraining memory formation and storage. It identified protein phosphatase 1 (PP1) and calcineurin as such molecular suppressors and demonstrated that these molecules need to be inhibited through training to relieve their suppressing action on neuronal activity necessary for memorisation. Her team was also able to demonstrate the detrimental effects of the excess of these molecules in the diseased and aged brain, highlighting their link to memory deficits and cognitive decline in aging. Another important finding was that PP1 is a key epigenetic regulator in neurons that controls the post-translational modification of histones and therefore genome activity. The role of such an enzyme in epigenetic regulation in relation to cognitive processes was not known before, these findings participated to found the new field of neuroepigenetics that emerged in late 2000, and opened unexpected therapeutic perspectives linking the epigenome to memory diseases.
Mansuy's current research examines the epigenetic basis of complex brain functions and physiological changes in mammals with a focus on the mechanisms of epigenetic inheritance. The goal is to determine how life experiences can influence mental and physical health across generations and what molecular mechanisms are involved. The research is focused on how adverse experiences in early life can lead to psychiatric and metabolic disorders. Mouse models and cellular systems are used to study non-coding RNAs, epigenetic factors and chromatin remodelling in the brain and germline, and elucidate how they are involved in the expression and subsequent transmission of environmentally-induced phenotypes. Her lab showed that the effects of traumatic stress in early life can be transmitted across multiple generations in mice and that RNA in sperm is a vector of transmission. Recent work showed that blood factors are involved in transmission mechanisms and have been validated in human subjects.