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Exploring the dendritic molecular machinery responsible for neuronal polarization

Project description

Mechanistic insight into neuronal polarisation

Neurons are highly polarised cells and consist of a single axon and several dendrites, which ensures directional flow of information in the nervous system. Dendrites receive incoming signals while axons transmit these signals to target cells. To address the critical question in neurobiology of how neurons acquire this polarity, the EU-funded SortAx project focuses on the role of endosomes. Researchers are investigating the mechanism by which endosomes sort and traffic proteins to the axon. Results will not only provide fundamental knowledge on neuron biology but will also help understand how these processes lead to neurodegenerative diseases like Alzheimer’s disease.

Objective

The high morphological and functional polarization of neuronal processes relies on exquisite mechanisms to accurately sort and traffic proteins to their rightful location. It is therefore of no surprise that accurate formation and function of neuronal circuits depends on these trafficking mechanisms, which are indeed often impaired in neurodegenerative disorders and normal aging.

During the past 30 years, researchers have been able to dissect the mechanisms required to target proteins to the dendritic plasma membrane, however our understanding of the mechanisms underlying the axonal polarization of proteins is rather incomplete. In this regard, a growing number of studies, including my work, suggests that dendritic endosomes are key sorting stations to direct neuronal cargoes to the axon. Yet, the molecular machinery of intracellular trafficking and endosomal sorting required remains to be uncovered.

In this proposal, I hypothesize that dendritic endosomes are key sorting stations for polarization of axonal cargoes. I therefore propose to elucidate the key axonal trafficking pathways of endogenous cargoes, the intracellular trafficking and endosomal machinery involved and assess their importance for axonal development and connectivity. Importantly, I will adopt an unbiased approach using cutting-edge technology to focus on the endogenous protein pool, which differs considerably from prior studies in the field, in which axonal trafficking route has been followed for a limited number of cargoes under overexpression conditions.

Given that abnormal axonal trafficking increases susceptibility to neurodegenerative diseases, including Alzheimer´s and Parkinson, with this project I will also contribute to the design of new therapies to alleviate neurodegeneration by deciphering the molecular mechanisms of axonal cargo trafficking.

Fields of science (EuroSciVoc)

Keywords

Programme(s)

Topic(s)

Funding Scheme

MSCA-IF - Marie Skłodowska-Curie Individual Fellowships (IF)

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Call for proposal

(opens in new window) H2020-MSCA-IF-2020

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Coordinator

CENTRO DE NEUROCIENCIAS E BIOLOGIACELULAR ASSOCIACAO
Net EU contribution
€ 147 815,04
Address
UNIVERSIDADE DE COIMBRA LARGO MARQUES DE POMBAL
3004 517 Coimbra
Portugal
Activity type
Research Organisations
Links
Total cost
€ 147 815,04