Impact Factor 3.519
2017 JCR, Clarivate Analytics 2018

Frontiers journals are at the top of citation and impact metrics

Original Research ARTICLE Provisionally accepted The full-text will be published soon. Notify me

Front. Endocrinol. | doi: 10.3389/fendo.2019.00424

Diet-induced obesity disturbs microglial immunometabolism in a time-of-day manner

 Irina V. Milanova1, Martin J. Kalsbeek1, Xiao-Lan Wang1, Nikita L. Korpel1,  Dirk Jan Stenvers1, Samantha E. Wolff1,  Paul De Goede1,  Annemieke C. Heijboer1, 2,  Eric Fliers1, Susanne E. La Fleur1, 3,  Andries Kalsbeek1, 3 and Chun-Xia Yi1*
  • 1University Medical Center Amsterdam, Netherlands
  • 2Vrije Universiteit Amsterdam, Netherlands
  • 3Netherlands Institute for Neuroscience (KNAW), Netherlands

Background: Disturbance of immunometabolic signaling is a key process involved in the progression of obesity. Microglia– the resident immune cells in the brain, initiate local immune responses. It is known that hypercaloric diets lead to microglial activation. Previously, we observed that hypothalamic microglial cells from mice fed high-fat diet (HFD) lose their day/night rhythm and are constantly activated. However, little is known about daily rhythmicity in microglial circadian, immune and metabolic functions, either in lean or obese conditions. Therefore, we hypothesized that HFD disturbs microglial immunometabolism in a day/night-dependent manner.
Methods: Obesity was induced in Wistar rats by feeding them HFD ad libitum for the duration of eight weeks. Microglia were isolated from HFD- and chow-fed control animals at six time points during 24h (every four hours starting 2h after lights on, i.e. Zeitgeber Time 2 (ZT2)). Gene expression was evaluated using quantitative RT-PCR. JTK_Cycle software was used to estimate daily rhythmicity. Statistical analysis was performed with two-way ANOVA test.
Results: Consumption of the obesogenic diet resulted in a 40 g significantly higher body weight gain in week eight, compared to chow diet (p<0.0001), associated with increased adiposity. We observed significant rhythmicity of circadian clock genes in microglia under chow conditions, which was partially lost in diet-induced obesity (DIO). Microglial immune gene expression also showed time-of-day differences, which were disrupted in HFD-fed animals. Microglia responded to the obesogenic conditions by a shift of substrate utilization with decreased glutamate and glucose metabolism in the active period of the animals, and an overall increase of lipid metabolism, as indicated by gene expression evaluation. Additionally, data on mitochondria bioenergetics and dynamics suggested an increased energy production in microglia during the inactive period on HFD. Finally, evaluation of monocyte functional gene expression showed small or absent effect of HFD on peripheral myeloid cells, suggesting a cell-specific microglial inflammatory response in DIO.
Conclusions: An obesogenic diet affects microglial immunometabolism in a time-of-day dependent manner. Given the central role of the brain in energy metabolism, a better knowledge of daily rhythms in microglial immunometabolism could lead to a better understanding of the pathogenesis of obesity.

Keywords: Microglia, Immunometabolism, Neuroinflammation, diet-induced obesity (DIO), High-fat (HF) diet, daily rhythm

Received: 12 Apr 2019; Accepted: 12 Jun 2019.

Edited by:

Vinicius F. Carvalho, Oswaldo Cruz Foundation (Fiocruz), Brazil

Reviewed by:

Yinghua Yu, Xuzhou Medical University, China
Licio A. Velloso, Campinas State University, Brazil  

Copyright: © 2019 Milanova, Kalsbeek, Wang, Korpel, Stenvers, Wolff, De Goede, Heijboer, Fliers, La Fleur, Kalsbeek and Yi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: MD, PhD. Chun-Xia Yi, University Medical Center Amsterdam, Amsterdam, Netherlands, c.yi@amsterdamumc.nl