Unravelling the crosstalk between Stellate cells and Kupffer cells and its role...
Unravelling the crosstalk between Stellate cells and Kupffer cells and its role in maintaining Stellate cell quiescence
Liver diseases are a global cause of mortality, accounting for two million deaths a year, of which half are attributed to liver fibrosis. Activated stellate cells are the major source of excessive extracellular-matrix deposition t...
ver más
Descripción del proyecto
Liver diseases are a global cause of mortality, accounting for two million deaths a year, of which half are attributed to liver fibrosis. Activated stellate cells are the major source of excessive extracellular-matrix deposition that drives fibrosis. The signals that convert quiescent stellate cells into pathogenic myofibroblasts remain largely unknown. Spatial analysis from the Guilliams lab has recently revealed that each quiescent stellate cell is paired with a Kupffer cell (KC) in the steady-state liver. This is because stellate cells play a central role in the maintenance of the KC pool. Indeed, upon KC depletion, stellate cells are the main cells promoting the recruitment of monocytes and their differentiation into KCs through the production of instructive signals. Interestingly, in fibrotic livers of mice and humans the progressive activation of stellate cells is coupled with the gradual disappearance of KCs and pro-fibrotic stellate cells are no longer paired with KCs. I hypothesize that the KC-Stellate cell relationship is mutually beneficial and essential for liver homeostasis and that, just as the stellate cell is the primary cell of the KC niche, KCs play a key role in preventing stellate cell activation. I have recently identified a mouse model in which the knock-down of a receptor for one of the main stellate cell-derived instructive factors leads to an almost complete absence of KCs in the liver. This yields a liver where most stellate cells are not paired with a KC. Interestingly, these mice spontaneously develop fibrosis, strengthening my hypothesis that KCs are crucial to maintain stellate cells quiescence. In this project, I will use scRNA-seq and spatial transcriptomics to study stellate cells paired or unpaired with a KC to define and study gene targets involved in the KC-stellate cell crosstalk, in the hope to unravel the KC-derived signals that maintain stellate cells in a quiescent state, as this may lead to novel anti-fibrotic strategies.
Seleccionando "Aceptar todas las cookies" acepta el uso de cookies para ayudarnos a brindarle una mejor experiencia de usuario y para analizar el uso del sitio web. Al hacer clic en "Ajustar tus preferencias" puede elegir qué cookies permitir. Solo las cookies esenciales son necesarias para el correcto funcionamiento de nuestro sitio web y no se pueden rechazar.
Cookie settings
Nuestro sitio web almacena cuatro tipos de cookies. En cualquier momento puede elegir qué cookies acepta y cuáles rechaza. Puede obtener más información sobre qué son las cookies y qué tipos de cookies almacenamos en nuestra Política de cookies.
Son necesarias por razones técnicas. Sin ellas, este sitio web podría no funcionar correctamente.
Son necesarias para una funcionalidad específica en el sitio web. Sin ellos, algunas características pueden estar deshabilitadas.
Nos permite analizar el uso del sitio web y mejorar la experiencia del visitante.
Nos permite personalizar su experiencia y enviarle contenido y ofertas relevantes, en este sitio web y en otros sitios web.