Increased plasma apoM levels impair triglyceride turnover in mice

Stefan Hajny, Anna Borup, Sara Elsoe, Christina Christoffersen*

*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

7 Citationer (Scopus)
25 Downloads (Pure)

Abstract

Objective: Apolipopmtein M (apoM) is an essential transporter of plasma Sphingosine-1 -Phosphate (S1P), typically attached to all lipoprotein classes, but with a majority bound to high density lipoproteins (HDL). ApoM-deficient mice display an increased activity in brown adipose tissue and a concomitant fast turnover of triglycerides. In what manner apoM/S1P affect the triglyceride metabolism is however still unknown and explored in the present study.

Methods: Triglyceride turnover and potentially associated metabolic pathways were studied in the female human apoM transgenic mouse model (apoM-Tg) with increased plasma apoM and SIP levels. The model was compared with wild type (WT) mice.

Results: ApoM-Tg mice had a reduced plasma triglyceride turnover rate and a lower free fatty acid uptake in subcutaneous adipocytes compared to WT mice. Screening for potential molecular mechanisms furthermore revealed a reduction in plasma lipase activity in apoM-Tg animals. Overexpression of apoM also reduced the plasma levels of fibroblast growth factor 21 (FGF21).

Conclusions: The study features the significant role of the apoM/S1P axis in maintaining a balanced triglyceride metabolism. Further, it also highlights the risk of inducing dyslipidaemia in patients receiving S1P-analouges and additionlly emphasizes the apoM/S1P axis as a potential therapeutic target in treatment of hypertriglyceridemia.

OriginalsprogEngelsk
Artikelnummer158969
TidsskriftB B A - Molecular and Cell Biology of Lipids
Vol/bind1866
Udgave nummer9
Antal sider9
ISSN1388-1981
DOI
StatusUdgivet - 2021

Citationsformater