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Sex-specific metabolic and functional differences in human umbilical vein endothelial cells from twin pairs

Authors :
Kai Kappert
Henryk Dreger
Benjamin Blaschke
Raphaela Fritsche-Guenther
Karl Stangl
Patrizia Brunner
Cornelia Bartsch
Andreas Benn
Yoann Gloaguen
Frederike Kramer
Jennifer A. Kirwan
Eric Witt
Elke Hammer
Angelika Vietzke
Verena Stangl
Petra Knaus
Hoang Giang Nguyen
Mario Lorenz
Source :
Atherosclerosis. 291:99-106
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

Background and aims Gonadal hormones are mainly thought to account for sex and gender differences in the incidence, clinical manifestation and therapy of many cardiovascular diseases. However, intrinsic sex differences at the cellular level are mostly overlooked. Here, we assessed sex-specific metabolic and functional differences between male and female human umbilical vein endothelial cells (HUVECs). Methods Cellular metabolism was investigated by bioenergetic studies (Seahorse Analyser) and a metabolomic approach. Protein levels were determined by Western blots and proteome analysis. Vascular endothelial growth factor (VEGF)-stimulated cellular migration was assessed by gap closure. HUVECs from dizygotic twin pairs were used for most experiments. Results No sex differences were observed in untreated cells. However, sexual dimorphisms appeared after stressing the cells by serum starvation and treatment with VEGF. Under both conditions, female cells had higher intracellular ATP and metabolite levels. A significant decline in ATP levels was observed in male cells after serum starvation. After VEGF, the ratio of glycolysis/mitochondrial respiration was higher in female cells and migration was more pronounced. Conclusions These results point to an increased stress tolerance of female cells. We therefore propose that female cells have an energetic advantage over male cells under conditions of diminished nutrient supply. A more favourable energy balance of female HUVECs after serum starvation and VEGF could potentially explain their stronger migratory capacity.

Details

ISSN :
00219150
Volume :
291
Database :
OpenAIRE
Journal :
Atherosclerosis
Accession number :
edsair.doi.dedup.....b762440e1f16fb11c021b08533879224
Full Text :
https://doi.org/10.1016/j.atherosclerosis.2019.10.007