A fluorescent perilipin 2 knock-in mouse model reveals a high abundance of lipid droplets in the developing and adult brain.
Détails
Télécharger: s41467-024-49449-w-1.pdf (7300.04 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
Etat: Public
Version: Final published version
Licence: CC BY 4.0
Document(s) secondaire(s)
Télécharger: 41467_2024_49449_MOESM1_ESM.pdf (61685.93 [Ko])
Etat: Public
Version: Supplementary document
Licence: Non spécifiée
Etat: Public
Version: Supplementary document
Licence: Non spécifiée
ID Serval
serval:BIB_A0D89CD09C50
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
A fluorescent perilipin 2 knock-in mouse model reveals a high abundance of lipid droplets in the developing and adult brain.
Périodique
Nature communications
ISSN
2041-1723 (Electronic)
ISSN-L
2041-1723
Statut éditorial
Publié
Date de publication
28/06/2024
Peer-reviewed
Oui
Volume
15
Numéro
1
Pages
5489
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: epublish
Publication Status: epublish
Résumé
Lipid droplets (LDs) are dynamic lipid storage organelles. They are tightly linked to metabolism and can exert protective functions, making them important players in health and disease. Most LD studies in vivo rely on staining methods, providing only a snapshot. We therefore developed a LD-reporter mouse by labelling the endogenous LD coat protein perilipin 2 (PLIN2) with tdTomato, enabling staining-free fluorescent LD visualisation in living and fixed tissues and cells. Here we validate this model under standard and high-fat diet conditions and demonstrate that LDs are highly abundant in various cell types in the healthy brain, including neurons, astrocytes, ependymal cells, neural stem/progenitor cells and microglia. Furthermore, we also show that LDs are abundant during brain development and can be visualized using live imaging of embryonic slices. Taken together, our tdTom-Plin2 mouse serves as a novel tool to study LDs and their dynamics under both physiological and diseased conditions in all tissues expressing Plin2.
Mots-clé
Animals, Perilipin-2/metabolism, Perilipin-2/genetics, Lipid Droplets/metabolism, Brain/metabolism, Mice, Neurons/metabolism, Gene Knock-In Techniques, Mice, Transgenic, Female, Luminescent Proteins/metabolism, Luminescent Proteins/genetics, Male, Astrocytes/metabolism, Diet, High-Fat, Mice, Inbred C57BL, Neural Stem Cells/metabolism, Neural Stem Cells/cytology, Microglia/metabolism
Pubmed
Open Access
Oui
Création de la notice
11/07/2024 13:42
Dernière modification de la notice
17/07/2024 6:19