Serotonin transporter-deficient mice display enhanced adipose tissue inflammation after chronic high-fat diet feeding.

Hoch, Johannes; Burkhard, Niklas; Zhang, Shanshan; Rieder, Marina; Marchini, Timoteo; Geest, Vincent; Krauel, Krystin; Zahn, Timm; Schommer, Nicolas; Hamad, Muataz Ali; Bauer, Carolina; Gauchel, Nadine; Stallmann, Daniela; Normann, Claus; Wolf, Dennis; Scharf, Rüdiger Eberhard; Duerschmied, Daniel; Schanze, Nancy (2023). Serotonin transporter-deficient mice display enhanced adipose tissue inflammation after chronic high-fat diet feeding. Frontiers in immunology, 14, p. 1184010. Frontiers Research Foundation 10.3389/fimmu.2023.1184010

[img]
Preview
Text
fimmu-14-1184010.pdf - Published Version
Available under License Creative Commons: Attribution (CC-BY).

Download (6MB) | Preview

INTRODUCTION

Serotonin is involved in leukocyte recruitment during inflammation. Deficiency of the serotonin transporter (SERT) is associated with metabolic changes in humans and mice. A possible link and interaction between the inflammatory effects of serotonin and metabolic derangements in SERT-deficient mice has not been investigated so far.

METHODS

SERT-deficient (Sert -/-) and wild type (WT) mice were fed a high-fat diet, starting at 8 weeks of age. Metabolic phenotyping (metabolic caging, glucose and insulin tolerance testing, body and organ weight measurements, qPCR, histology) and assessment of adipose tissue inflammation (flow cytometry, histology, qPCR) were carried out at the end of the 19-week high-fat diet feeding period. In parallel, Sert -/- and WT mice received a control diet and were analyzed either at the time point equivalent to high-fat diet feeding or as early as 8-11 weeks of age for baseline characterization.

RESULTS

After 19 weeks of high-fat diet, Sert -/- and WT mice displayed similar whole-body and fat pad weights despite increased relative weight gain due to lower starting body weight in Sert -/-. In obese Sert -/- animals insulin resistance and liver steatosis were enhanced as compared to WT animals. Leukocyte accumulation and mRNA expression of cytokine signaling mediators were increased in epididymal adipose tissue of obese Sert -/- mice. These effects were associated with higher adipose tissue mRNA expression of the chemokine monocyte chemoattractant protein 1 and presence of monocytosis in blood with an increased proportion of pro-inflammatory Ly6C+ monocytes. By contrast, Sert -/- mice fed a control diet did not display adipose tissue inflammation.

DISCUSSION

Our observations suggest that SERT deficiency in mice is associated with inflammatory processes that manifest as increased adipose tissue inflammation upon chronic high-fat diet feeding due to enhanced leukocyte recruitment.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Cardiovascular Disorders (DHGE) > Clinic of Cardiology

UniBE Contributor:

Rieder, Marina Hedwig

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1664-3224

Publisher:

Frontiers Research Foundation

Language:

English

Submitter:

Pubmed Import

Date Deposited:

02 Aug 2023 07:32

Last Modified:

20 Aug 2023 02:37

Publisher DOI:

10.3389/fimmu.2023.1184010

PubMed ID:

37520561

Uncontrolled Keywords:

adipose tissue inflammation metabolic syndrome obesity serotonin serotonin transporter

BORIS DOI:

10.48350/185153

URI:

https://boris.unibe.ch/id/eprint/185153

Actions (login required)

Edit item Edit item
Provide Feedback