Descripción del proyecto
Mantener la aptitud celular en oocitos latentes
Las células germinales femeninas, los oocitos, pueden sobrevivir durante largos periodos conservando la capacidad de crear un nuevo organismo. Los mecanismos moleculares que permiten a los oocitos eludir el envejecimiento celular son poco conocidos. El equipo del proyecto ACTIVEDORMANCY, financiado por el CEI, tiene como objetivo descubrir los mecanismos que subyacen al mantenimiento de la aptitud celular y cómo estos mecanismos se ven afectados por el envejecimiento, empleando tecnologías de imagen y ómicas de última generación. La latencia de los oocitos implica al menos dos mecanismos únicos descubiertos recientemente: la supresión del complejo mitocondrial I y la activación constitutiva de la respuesta mitocondrial a las proteínas no plegadas. En el proyecto actual se estudiarán las adaptaciones metabólicas de la supervivencia celular sin complejo mitocondrial I, las proteínas oocitarias de larga vida y su regulación, y los mecanismos de control de calidad en oocitos latentes.
Objetivo
Female germ cells, oocytes, have the remarkable ability to survive for long periods of time, up to 50 years in humans, while retaining the ability to give rise to a new organism. We know surprisingly little about the molecular mechanisms through which oocytes alleviate cellular ageing, and why such mechanisms eventually fail with advanced age.
The goal of this research proposal is to reveal both the mechanisms dormant oocytes employ to maintain cellular fitness and how ageing affects these mechanisms, combining biochemical perturbations with imaging and state-of-the-art -omics techniques. We have recently discovered that oocyte dormancy involves two mechanisms not reported in any animal cell type before: the suppression of mitochondrial complex I, and the constitutive activation of mitochondrial unfolded protein response. These discoveries point to a set of poorly understood strategies that oocytes use to minimise damage to their cellular components during their long lifespan. In this project, we focus on three new interlinked directions to reveal mechanisms that dormant oocytes employ to keep a ‘youthful’ cytoplasm: 1) Characterise the metabolic adaptations that enable life without mitochondrial complex I 2) Study extremely long-lived oocyte proteins and their regulation 3) Identify and characterise the quality control mechanisms that eventually fail in dormant oocytes to impact fertility. We will use oocytes from frogs, mice, and humans which are complementary in their ease of handling and relevance to human physiology.
One of the biggest problems developed nations face is late-motherhood and associated fertility problems due to ageing oocytes. >25% of female fertility problems are unexplained, pointing to a huge gap in our understanding of female reproduction. This proposal will help fill this gap by studying longevity mechanisms in dormant oocytes. It will further provide insights into the metabolic adaptations of long-lived cells, female fertility, and ageing.
Ámbito científico
Palabras clave
Programa(s)
- HORIZON.1.1 - European Research Council (ERC) Main Programme
Régimen de financiación
HORIZON-ERC - HORIZON ERC GrantsInstitución de acogida
08003 Barcelona
España