26.08.2015

Portrait Moritz Rossner

Prof. Dr. Moritz Rossner

Molecular Neurobiology
LMU München, Nußbaumstr. 7
D-80366 Munich
Fon: +49 89 - 4400-55891
Fax: +49 89 - 4400-55779 E-Mail: Mail an Rossner

Portrait Oliver Schlüter

Dr. Dr. Oliver Schlüter

Molecular Neurobiology
ENI Göttingen, Grisebachstr. 5
D-37077 Göttingen
Fon: +49 551 - 39-10374
Fax: +49 551 - 39-12346
E-Mail: Mail an Schlueter



Molecular and neuronal pathway-specific analysis of pathognomonic signatures in two-hit schizophrenia mouse models combining environmental and genetic risk factors

Increasing evidence suggest that disturbed functional connectivity across brain regions is implicated in the etiology of psychotic diseases, including schizophrenia and bipolar disorders. Cognitive symptoms are a common hallmark of this heterogeneous group of diseases. The underlying mechanisms, however, remain still largely elusive. Human imaging data and studies in animal models suggest that impaired interactions of the ventral Hippocampus (vHi) and the medial prefrontal Cortex (mPFC) could be associated with cognitive deficits in schizophrenia.

Thus, we now want to apply optophysiology on brain slices of neuron-type reporter mice in combination with molecular profiling techniques to characterize pathway-specific mechanisms underlying vHi-mPFC interactions. Therefore, we will make use of a well characterized mouse model for the schizophrenia risk gene TCF4 named Tcf4tg crossed with fluorescent reporter mice for endocannabinoid receptor-positive interneurons and parvalbumin-positive interneurons, in which cell-type specific optophysiological recordings and molecular profiling can be performed.

We could previously show that Tcf4tg mice display several behavioral endophenotypes of Sz, including Hi dependent cognitive deficits and sensori-motor gating. In particular, cognitive deficits depending on the mPFC are amplified when Tcf4tg mice are subjected to psychosocial stress modeling gene x environment (GxE) interactions of schizophrenia. If successful, we will identify the cellular and molecular substrates underlying disturbed vHi-mPFC connectivity in the Tcf4tg GxE model which would pave the way for follow-up studies in other models in the future.