Skip to main content
Go to the home page of the European Commission (opens in new window)
English en
CORDIS - EU research results
CORDIS

Tau, a molecular modulator of neuronal energy managment

Project description

A new role for Tau as neuronal energy modulator

The Tau protein acts to stabilise microtubules and support intracellular transport in neurons. However, Tau missorting and aggregation in neurons are key hallmarks of neurodegenerative diseases (NDDs) such as Alzheimer’s disease. The ERC-funded EnergizeTau project investigates a transformative hypothesis that Tau aggregation is a physiological response to bioenergetic challenges such as hyperexcitation or energy deprivation. The idea is that energy-demanding functions like synaptic activity, ATP production and protein translation are affected, leading to prolonged energetic stress, irreversible Tau aggregation and neuronal silencing. Researchers will follow a multidisciplinary approach to study how Tau orchestrates neuronal energy management. Project results could redefine Tau biology and offer new avenues to prevent and treat NDDs.

Objective

"The intraneuronal somatodendritic ""missorting"" and aggregation of Tau are pathological hallmarks in neurodegenerative diseases (NDDs) like and Alzheimer's disease (AD), and are thought to be drivers of neurotoxicity. That NDDs manifesting with Tau ""missorting"" present with (neuro)metabolic abnormalities, often prior to pathology onset, is largely overlooked. EnergizeTau investigates the ground-breaking new idea that the somatodendritic re-sorting of Tau is a physiological response to bioenergetic challenges faced by excitatory neurons, such as hyperexcitation or energy deprivation. In its proposed role as modulator of neuronal energy management, Tau modulates the cellular energy demand through molecular interactions with key cellular functions, e.g. synaptic activity, ATP production and protein translation, and alters the neuronal metabolism. Continued energetic stress in disease results in irreversible ""silencing"" and Tau aggregation in affected neurons. Using my uniquely broad Tau expertise, we decipher how Tau interferes with energy demanding cellular functions to modulate neuronal energy household downstream of bioenergetic stress. Light-induced Tau expression and CRISPR-edited human neurons enable to study Tau's molecular actions by interactomics and single-molecule imaging, and the effects on cellular functions. Tau's influence on the neuronal metabolism is determined by longitudinal live cell metabolite imaging and spatial transcriptomics in human brains, and the impact on gene and chromatin regulation by Cut&Tag and DNA-FISH. Whether stressors converge on energy limitation as a driver of Tau re-sorting is assessed by high-content metabolite imaging. EnergizeTau introduces the metabolic component of Tau (patho)biology and generates a paradigm shift in NDD research. It creates space for re-thinking hallmark protein pathology in NDDs, and has the potential to result in new approaches targeting the neuronal energy metabolism to prevent and treat NDDs."

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-ERC - HORIZON ERC Grants

See all projects funded under this funding scheme

Call for proposal

(opens in new window) ERC-2023-COG

See all projects funded under this call

Host institution

DEUTSCHES ZENTRUM FUR NEURODEGENERATIVE ERKRANKUNGEN EV
Net EU contribution
€ 2 194 940,00
Address
VENUSBERG-CAMPUS 1/99
53127 Bonn
Germany
Region
Nordrhein-Westfalen Köln Bonn, Kreisfreie Stadt
Activity type
Research Organisations
Links
Total cost
€ 2 194 940,00

Beneficiaries (1)