Metabolic consequences for mice lacking Endosialin: LC-MS/MS-based metabolic phenotyping of serum from C56Bl/6J Control and CD248 knock-out mice

Metabolomics. 2021 Jan 18;17(2):14. doi: 10.1007/s11306-020-01764-1.

Abstract

Introduction: The Endosialin/CD248/TEM1 protein is expressed in adipose tissue and its expression increases with obesity. Recently, genetic deletion of CD248 has been shown to protect mice against atherosclerosis on a high fat diet.

Objectives: We investigated the effect of high fat diet feeding on visceral fat pads and circulating lipid profiles in CD248 knockout mice compared to controls.

Methods: From 10 weeks old, CD248-/- and +/+ mice were fed either chow (normal) diet or a high fat diet for 13 weeks. After 13 weeks the metabolic profiles and relative quantities of circulating lipid species were assessed using ultra high performance liquid chromatography-quadrupole time-of flight mass spectrometry (UHPLC-MS) with high resolution accurate mass (HRAM) capability.

Results: We demonstrate a specific reduction in the size of the perirenal fat pad in CD248-/- mice compared to CD248+/+, despite similar food intake. More strikingly, we identify significant, diet-dependent differences in the serum metabolic phenotypes of CD248 null compared to age and sex-matched wildtype control mice. Generalised protection from HFD-induced lipid accumulation was observed in CD248 null mice compared to wildtype, with particular reduction noted in the lysophosphatidylcholines, phosphatidylcholines, cholesterol and carnitine.

Conclusions: Overall these results show a clear and protective metabolic consequence of CD248 deletion in mice, implicating CD248 in lipid metabolism or trafficking and opening new avenues for further investigation using anti-CD248 targeting agents.

Keywords: CD248; Endosialin; HRAM UHPLC–MS/MS; High fat diet.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / metabolism
  • Animals
  • Antigens, CD / genetics*
  • Antigens, CD / metabolism*
  • Antigens, Neoplasm
  • Carnitine / metabolism
  • Cholesterol
  • Chromatography, High Pressure Liquid
  • Chromatography, Liquid*
  • Diet, High-Fat
  • Female
  • Intra-Abdominal Fat / metabolism
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Knockout
  • Neoplasm Proteins / genetics*
  • Neoplasm Proteins / metabolism*
  • Obesity / metabolism
  • Phosphatidylcholines / metabolism
  • Tandem Mass Spectrometry*
  • Transcriptome

Substances

  • Antigens, CD
  • Antigens, Neoplasm
  • CD248 protein, mouse
  • Neoplasm Proteins
  • Phosphatidylcholines
  • tumor endothelial marker 1, mouse
  • Cholesterol
  • Carnitine