Katalog Plus
Bibliothek der Frankfurt UAS
Bald neuer Katalog: sichern Sie sich schon vorab Ihre persönlichen Merklisten im Nutzerkonto: Anleitung.
Dieses Ergebnis aus BASE kann Gästen nicht angezeigt werden.  Login für vollen Zugriff.

The Nuclear Receptor LXR Limits Bacterial Infection of Host Macrophages through a Mechanism that Impacts Cellular NAD Metabolism

Title: The Nuclear Receptor LXR Limits Bacterial Infection of Host Macrophages through a Mechanism that Impacts Cellular NAD Metabolism
Authors: Matalonga, J; Glaria, E; Bresque, M; Escande, C; Carbó, JM; Kiefer, K; Vicente, R; León, TE; Beceiro, S; Pascual-García, M; Serret, J; Sanjurjo, L; Morón-Ros, S; Riera, A; Paytubi, S; Juarez, A; Sotillo, F; Lindbom, L; Caelles, C; Sarrias, M-R; Sancho, J; Castrillo, A; Chini, EN; Valledor, AF
Source: Cell Reports , 18 (5) pp. 1241-1255. (2017)
Publication Year: 2017
Collection: University College London: UCL Discovery
Subject Terms: macrophage; nuclear receptor; LXR; bacterial infection; NAD; cytoskeleton; CD38
Description: Macrophages exert potent effector functions against invading microorganisms but constitute, paradoxically, a preferential niche for many bacterial strains to replicate. Using a model of infection by Salmonella Typhimurium, we have identified a molecular mechanism regulated by the nuclear receptor LXR that limits infection of host macrophages through transcriptional activation of the multifunctional enzyme CD38. LXR agonists reduced the intracellular levels of NAD+ in a CD38-dependent manner, counteracting pathogen-induced changes in macrophage morphology and the distribution of the F-actin cytoskeleton and reducing the capability of non-opsonized Salmonella to infect macrophages. Remarkably, pharmacological treatment with an LXR agonist ameliorated clinical signs associated with Salmonella infection in vivo, and these effects were dependent on CD38 expression in bone-marrow-derived cells. Altogether, this work reveals an unappreciated role for CD38 in bacterial-host cell interaction that can be pharmacologically exploited by activation of the LXR pathway.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/1546199/1/Matalonga%20et%20al%202017_CD38.pdf; https://discovery.ucl.ac.uk/id/eprint/1546199/
Availability: https://discovery.ucl.ac.uk/id/eprint/1546199/1/Matalonga%20et%20al%202017_CD38.pdf; https://discovery.ucl.ac.uk/id/eprint/1546199/
Rights: open
Accession Number: edsbas.25DED41B
Database: BASE