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Transcriptional Regulation Assessed in Neuronal Subtypes in three major interrelated Psychiatric disorders

Project description

Organoid models for psychiatric disorders

Schizophrenia, bipolar disorder, and major depressive disorder are interconnected psychiatric conditions with shared neurobiology. However, their underlying mechanisms remain poorly understood. Existing testing models face significant limitations, highlighting the need for new approaches. The ERC-funded TRANS-PSYCH project aims to develop organoid models for these psychiatric disorders by targeting upstream transcription factors critical for cell type differentiation and neuronal network formation. The central hypothesis is that these transcription factors can serve as targets for modelling these disorders in brain organoids. The project will leverage multi-omics profiling on a high-quality collection of psychiatric human brain tissue to identify key transcription factors, which will then be targeted in brain organoid systems to create neurobiological models of psychiatric disorders.

Objective

Schizophrenia (SCZ), bipolar disorder (BP), and Major Depressive Disorder (MD) are three major psychiatric disorders that affect mood, thinking, and behavior. These disorders are strongly genetically intercorrelated, and exhibit pronounced clinical overlap, suggesting that they are different manifestations of a shared underlying neurobiology, along a spectrum. However, the neurobiological mechanisms and pathophysiology of these disorders are still poorly understood, limiting effective drug discovery. There is an urgent need for new models for drug testing, as animal models have major limitations, and current psychiatric organoids systems are dependent on patient derived stem cells, in which technical, genetic and biological diversity confound the interpretation, and obscure the underlying neuropathology. The major challenge of this ERC proposal is to develop organoid models for psychiatric disorders by targeting upstream transcription factors. Transcription factors are key molecules that drive cell type differentiation including neuronal network formation. Hence, the central hypothesis of this ERC proposal is that neuronal subtype associated transcription factors can function as targets to model these disorders using brain organoids. However, the neuronal transcriptional regulators that mediate these disorders are currently unknown, and difficult to identify. Novel genomics technologies allow for an unbiased characterization of the brain in order to detect cell types and genes that are dysregulated in disease, and can be used to identify putative upstream transcription factors. Here, I propose a selection of multi-omics profiling - strategies to a unique collection of high quality psychiatric human brain tissue aimed at reliably identifying key upstream transcription factors. We will subsequently target those transcription factors in brain organoid systems to establish neurobiological models of these disorders.

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HORIZON-ERC - HORIZON ERC Grants

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Call for proposal

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(opens in new window) ERC-2022-STG

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Host institution

ACADEMISCH ZIEKENHUIS GRONINGEN
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 1 499 999,00
Address
HANZEPLEIN 1
9713 GZ Groningen
Netherlands

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Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 1 499 999,00

Beneficiaries (1)

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