Inter-tissue expression patterns of the key metabolic biomarker PGC-1α in severely obese individuals: Implication in obesity-induced disease.
Adipose Tissue
/ metabolism
Adult
Antigens, CD
/ metabolism
Antigens, Differentiation, Myelomonocytic
/ metabolism
Bariatric Surgery
/ methods
Biomarkers
/ metabolism
Diabetes Mellitus
/ epidemiology
Fatty Acids
/ metabolism
Female
Humans
Immunohistochemistry
/ methods
Inflammation
/ metabolism
Intra-Abdominal Fat
/ metabolism
Male
Metabolic Syndrome
/ epidemiology
Middle Aged
Mitochondria
/ metabolism
Muscle, Skeletal
/ metabolism
Obesity, Morbid
/ complications
Oxidative Phosphorylation
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
/ metabolism
Peroxisome Proliferator-Activated Receptors
/ metabolism
Obesity
PGC-1α
diabetes
metabolic syndrome
peroxisome proliferator-activated receptor gamma (PPAR-γ) coactivator 1α
Journal
Hellenic journal of cardiology : HJC = Hellenike kardiologike epitheorese
ISSN: 2241-5955
Titre abrégé: Hellenic J Cardiol
Pays: Netherlands
ID NLM: 101257381
Informations de publication
Date de publication:
Historique:
received:
13
06
2018
revised:
29
07
2018
accepted:
03
08
2018
pubmed:
24
8
2018
medline:
2
6
2020
entrez:
24
8
2018
Statut:
ppublish
Résumé
PGC-1α is already known as a significant regulator of mitochondrial biogenesis, oxidative phosphorylation and fatty acid metabolism. Our study focuses on the role of PGC1α in morbid obesity, in five different tissues, collected from 50 severely obese patients during planned bariatric surgery. The investigated tissues included subcutaneous adipose tissue (SAT), visceral adipose tissue (VAT), skeletal muscle (SM), extramyocellular adipose tissue (EMAT) and liver. PGC1α expression was investigated with immunohistochemistry and evaluated with microscopy. Our findings highlighted significant positive inter-tissue correlations regarding PGC-1α expression between several tissue pairs (VAT-SAT, VAT-SM, VAT-EMAT, SAT-SM, SAT-EMAT, SM-EMAT). Moreover, we found significant negative correlations between PGC1α expression in VAT with CD68 expression in skeletal muscle and EMAT, implying a possible protective role of PGC1α against obesity-induced inflammation. Unmasking the inter-tissue communication networks regarding PGC-1α expression in morbid obesity, will give more insight into its significant role in obesity-induced diseases. PGC1α could potentially represent a future preventive and therapeutic target against obesity-induced disease, probably through enhancing mitochondrial biogenesis and metabolism.
Identifiants
pubmed: 30138744
pii: S1109-9666(18)30252-5
doi: 10.1016/j.hjc.2018.08.002
pii:
doi:
Substances chimiques
Antigens, CD
0
Antigens, Differentiation, Myelomonocytic
0
Biomarkers
0
CD68 antigen, human
0
Fatty Acids
0
PPARGC1A protein, human
0
Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
0
Peroxisome Proliferator-Activated Receptors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
282-293Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2018 Hellenic Society of Cardiology. Published by Elsevier B.V. All rights reserved.