Persistent low body weight in humans is associated with higher mitochondrial activity in white adipose tissue. Issue 3 (2nd August 2019)

• Record Type: Journal Article
• Authors: Ling, Yiin; Carayol, Jérôme; Galusca, Bogdan; Canto, Carles; Montaurier, Christophe; Matone, Alice; Vassallo, Irene; Minehira, Kaori; Alexandre, Virginie; Cominetti, Ornella; Núñez Galindo, Antonio; Corthésy, John; Dayon, Loïc; Charpagne, Aline; Métairon, Sylviane; Raymond, Frédéric; Descombes, Patrick; Casteillo, François; Peoc'h, Michel; Palaghiu, Radu; Féasson, Léonard; Boirie, Yves; Estour, Bruno; Hager, Jörg; Germain, Natacha; Gheldof, Nele
• Is Part Of: American journal of clinical nutrition. Volume 110:Issue 3(2019)
• Page Start: 605
• Page End: 616
• Publication Date: 2019-08-02
• Subjects: constitutional thinness -- futile lipid cycling -- mitochondria -- proteomics -- respiration -- transcriptome analysis -- white adipose tissue; Diet therapy -- Periodicals; Nutrition -- Periodicals; Dietetics -- Periodicals; 613.205
• DOI: 10.1093/ajcn/nqz144
• Languages: English
• ISSNs: 0002-9165

Abstract

ABSTRACT: Background: Constitutional thinness (CT) is a state of low but stable body weight (BMI ≤18 kg/m 2 ). CT subjects have normal-range hormonal profiles and food intake but exhibit resistance to weight gain despite living in the modern world's obesogenic environment. Objective: The goal of this study is to identify molecular mechanisms underlying this protective phenotype against weight gain. Methods: We conducted a clinical overfeeding study on 30 CT subjects and 30 controls (BMI 20–25 kg/m 2 ) matched for age and sex. We performed clinical and integrative molecular and transcriptomic analyses on white adipose and muscle tissues. Results: Our results demonstrate that adipocytes were markedly smaller in CT individuals (mean ± SEM: 2174 ± 142 μm 2 ) compared with controls (3586 ± 216 μm 2 ) ( P < 0.01). The mitochondrial respiratory capacity was higher in CT adipose tissue, particularly at the level of complex II of the electron transport chain (2.2-fold increase; P < 0.01). This higher activity was paralleled by an increase in mitochondrial number (CT compared with control: 784 ± 27 compared with 675 ± 30 mitochondrial DNA molecules per cell; P < 0.05). No evidence for uncoupled respiration or "browning" of the white adipose tissue was found. In accordance with the mitochondrial differences, CT subjects had a distinct adipose transcriptomic profile [62 differentially expressed genes (false discovery rate of 0.1 and log fold change >0.75)], with many differentially expressed genes associating with positive metabolic outcomes. Pathway analyses revealed an increase in fatty acid oxidation ( P = 3 × 10 −04 ) but also triglyceride biosynthesis ( P = 3.6 × 10 −04 ). No differential response to the overfeeding was observed in the 2 groups. Conclusions: The distinct molecular signature of the adipose tissue in CT individuals suggests the presence of augm ented futile lipid cycling, rather than mitochondrial uncoupling, as a way to increase energy expenditure in CT individuals. We propose that increased mitochondrial function in adipose tissue is an important mediator in sustaining the low body weight in CT individuals. This knowledge could ultimately allow more targeted approaches for weight management treatment strategies. This trial was registered at clinicaltrials.gov as NCT02004821.