ABSTRACT
The central nervous system regulates systemic immune responses by integrating the physiological and behavioral constraints faced by an individual. Corticosterone (CS), the release of which is controlled in the hypothalamus by the paraventricular nucleus (PVN), is a potent negative regulator of immune responses. Using the mouse model, we report that the parabrachial nucleus (PB), an important hub linking interoceptive afferent information to autonomic and behavioral responses, also integrates the pro-inflammatory cytokine IL-1ß signal to induce the CS response. A subpopulation of PB neurons, directly projecting to the PVN and receiving inputs from the vagal complex (VC), responds to IL-1ß to drive the CS response. Pharmacogenetic reactivation of these IL-1ß-activated PB neurons is sufficient to induce CS-mediated systemic immunosuppression. Our findings demonstrate an efficient brainstem-encoded modality for the central sensing of cytokines and the regulation of systemic immune responses.
Subject(s)
Cytokines , Parabrachial Nucleus , Animals , Mice , Corticosterone , Feedback , Hypothalamus , Paraventricular Hypothalamic Nucleus/physiologyABSTRACT
TITLE: Mucoviscidose: Quand les bactéries coopèrent pour mieux régner - La recherche en microbiologie vue par les étudiants de l'ENS de Lyon. ABSTRACT: Le dossier que nous présentons a été rédigé par les étudiantes et étudiants de Master 1 de Biologie de l'École Normale Supérieure de Lyon à l'issue de l'UE Microbiologie Moléculaire et Structurale (2020-2021). Le Master de Biologie de l'ENS de Lyon accueille chaque année environ 40 étudiants en M1 et en M2 et propose une formation de haut niveau à la recherche en biosciences. Chaque étudiant y construit son parcours à la carte, en choisissant ses options parmi un large panel de modules, favorisant ainsi une approche pluridisciplinaire des sciences du vivant, et cela en relation étroite avec les laboratoires de recherche du tissu local, national et international. En participant à diverses activités scientifiques liées aux UE de leur formation, les étudiants préparent également l'obtention du Diplôme de l'ENS de Lyon, qui valide leur scolarité à l'ENS. La rédaction du présent dossier, qui vise à transmettre de façon claire les messages issus d'une sélection d'articles scientifiques publiés récemment dans le domaine de la microbiologie, constitue l'une de ces activités connexes proposées aux étudiants.
Subject(s)
Cystic Fibrosis , Bacteria , Humans , StudentsABSTRACT
Links between olfactory sensory function and effect have been well established. A robust literature exists in both humans and animals showing that disrupting olfaction sensory function can elicit disordered mood state, including serve as a model of depression. Despite this, considerably less is known regarding the directionality and neural basis of this relationship, e.g. whether disruptions in sensory function precede and contribute to altered mood or if altered mood state precipitates changes in olfactory perception. Further, the neural basis of altered olfactory function in depression remains unclear. In conjunction with clinical studies, animal models represent a valuable tool to understand the relationship between altered mood and olfactory sensory function. Here, we review the relevant literature assessing olfactory performance in depression in humans and in rodent models of depressive-like behavioral states. Rodents allow for detailed characterization of alterations in olfactory perception, manipulation of experiential events that elicit depressive-like phenotypes, and allow for interrogation of potential predictive markers of disease and the cellular basis of olfactory impairments associated with depressive-like phenotypes. We synthesize these findings to identify paths forward to investigate and understand the complex interplay between depression and olfactory sensory function.
