Decoration of myocellular lipid droplets with perilipins as a marker for in vivo lipid droplet dynamics: A super-resolution microscopy study in trained athletes and insulin resistant individuals.
Adult
Aged
Athletes
Biomarkers
/ analysis
Biopsy
Diabetes Mellitus, Type 2
/ metabolism
Endurance Training
Fatty Acids
/ metabolism
Humans
Insulin
/ metabolism
Insulin Resistance
Lipase
/ analysis
Lipid Droplets
/ metabolism
Lipolysis
Male
Microscopy, Confocal
/ methods
Middle Aged
Mitochondria
/ metabolism
Muscle Fibers, Skeletal
/ cytology
Oxidation-Reduction
Perilipin-2
/ analysis
Perilipin-5
/ analysis
Young Adult
Lipid droplet dynamics
Perilipin 2
Perilipin 5
Skeletal muscle
Super-resolution microscopy
athlete's paradox
Journal
Biochimica et biophysica acta. Molecular and cell biology of lipids
ISSN: 1879-2618
Titre abrégé: Biochim Biophys Acta Mol Cell Biol Lipids
Pays: Netherlands
ID NLM: 101731727
Informations de publication
Date de publication:
02 2021
02 2021
Historique:
received:
20
07
2020
revised:
29
10
2020
accepted:
30
10
2020
pubmed:
8
11
2020
medline:
24
4
2021
entrez:
7
11
2020
Statut:
ppublish
Résumé
In many different cell types neutral lipids can be stored in lipid droplets (LDs). Nowadays, LDs are viewed as dynamic organelles, which store and release fatty acids depending on energy demand (LD dynamics). Proteins like perilipin 2 (PLIN2) and PLIN5 decorate the LD membrane and are determinants of LD lipolysis and fat oxidation, thus affecting LD dynamics. Trained athletes and type 2 diabetes (T2D) patients both have high levels of intramyocellular lipid (IMCL). While IMCL content scales negatively with insulin resistance, athletes are highly insulin sensitive in contrast to T2D patients, the so-called athlete's paradox. Differences in LD dynamics may be an underlying factor explaining the athlete's paradox. We aimed to quantify PLIN2 and PLIN5 content at individual LDs as a reflection of the ability to switch between fatty acid release and storage depending on energy demand. Thus, we developed a novel fluorescent super-resolution microscopy approach and found that PLIN2 protein abundance at the LD surface was higher in T2D patients than in athletes. Localization of adipocyte triglyceride lipase (ATGL) to the LD surface was lower in LDs abundantly decorated with PLIN2. While PLIN5 abundance at the LD surface was similar in athletes and T2D patients, we have observed previously that the number of PLIN5 decorated LDs was higher in athletes, indicating more LDs in close association with mitochondria. Thus, in athletes interaction of LDs with mitochondria was more pronounced and LDs have the protein machinery to be more dynamic, while in T2D patients the LD pool is more inert. This observation contributes to our understanding of the athlete's paradox.
Identifiants
pubmed: 33160079
pii: S1388-1981(20)30244-4
doi: 10.1016/j.bbalip.2020.158852
pii:
doi:
Substances chimiques
Biomarkers
0
Fatty Acids
0
Insulin
0
PLIN2 protein, human
0
PLIN5 protein, human
0
Perilipin-2
0
Perilipin-5
0
Lipase
EC 3.1.1.3
PNPLA2 protein, human
EC 3.1.1.3
Types de publication
Comparative Study
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
158852Informations de copyright
Copyright © 2020 The Author(s). Published by Elsevier B.V. All rights reserved.