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Development of hypothalamic circuits for the control of homeostasis

Descrizione del progetto

Obesità infantile e sviluppo neuronale

L’obesità è un onere globale e l’obesità infantile viene riconosciuta come un grave problema di salute. Il progetto ONTOGENY, finanziato dall’UE, si propone di scoprire i processi di sviluppo importanti per il controllo dell’omeostasi energetica. I neuroni del peptide ipotalamico correlato all’aguti (AgRP, Agouti-Related Peptide) potrebbero stimolare l’assunzione di cibo, mentre i neuroni della proopiomelanocortina (POMC) inibiscono il comportamento alimentare. Il progetto studierà l’ontogenesi tardiva dei neuroni AgRP e POMC, misurando la loro attività durante lo sviluppo del topo in risposta ai nutrienti e agli ormoni coinvolti nell’omeostasi energetica. Infine, fornirà importanti informazioni sullo sviluppo dei neuroni AgRP e POMC in condizioni rilevanti per l’obesità infantile e la disregolazione metabolica.

Obiettivo

Obesity is a significant global burden that is associated with adverse health outcomes. Adults are not alone in their struggles with obesity. Children now accumulate fat at an alarming rate, making childhood obesity a major health problem. Unfortunately, we do not know enough about the pathophysiology of these conditions to propose appropriate prevention strategies and more effective therapeutic approaches. In this ERC StG proposal, our goal is to discover the developmental processes important for proper con-trol of energy homeostasis. We will study Agrp and POMC neurons, located in the arcuate nucleus of the hypothalamus, that are heavily involved with control of energy homeostasis. Agrp and POMC neu-rons have delayed postnatal development, maturing their axonal projections around the third postnatal week in rodents. Here, we will study in detail this late ontogeny of Agrp and POMC neurons. In Aim 1, we will use novel approaches to measure Agrp and POMC neuronal activity during mouse development in response to nutrients and hormones involved in energy homeostasis. In Aim 2, we will use whole-brain imaging techniques to determine the anatomical development of Agrp and POMC neuronal projec-tions. We will also study the importance of a specific neuronal circuit in neonates to the development of obesity. Finally, in Aim 3, we will identify critical molecular mechanisms involved in the ontogeny of Agrp and POMC neurons by investigating their translatome over the course of postnatal development. Overall, this project will provide novel insights into Agrp and POMC neuron development in conditions relevant to childhood obesity and metabolic dysregulation. The functional, anatomical and molecular mechanisms illuminated here will provide the foundation for future studies aimed to dissect the devel-opment of other homeostatic systems.

Meccanismo di finanziamento

ERC-STG - Starting Grant

Istituzione ospitante

THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD
Contribution nette de l'UE
€ 1 999 973,00
Indirizzo
WELLINGTON SQUARE UNIVERSITY OFFICES
OX1 2JD Oxford
Regno Unito

Mostra sulla mappa

Regione
South East (England) Berkshire, Buckinghamshire and Oxfordshire Oxfordshire
Tipo di attività
Higher or Secondary Education Establishments
Collegamenti
Costo totale
€ 1 999 973,00

Beneficiari (1)