Dietary macronutrients and the aging liver sinusoidal endothelial cell

• Published in: American Journal of Physiology - Heart and Circulatory Physiology
• Main Author: Cogger V.C.; Mohamad M.; Solon-Biet S.M.; Senior A.M.; Warren A.; O’Reilly J.N.; Tung B.T.; Svistounov D.; McMahon A.C.; Fraser R.; Raubenheimer D.; Holmes A.J.; Simpson S.J.; Le Couteur D.G.
• Format: Article
• Language: English
• Published: American Physiological Society 2016
• Online Access: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84983801280&doi=10.1152%2fajpheart.00949.2015&partnerID=40&md5=fd41502680e29aff99a210d359cfa9eb

Fenestrations are pores within the liver sinusoidal endothelial cells (LSECs) that line the sinusoids of the highly vascularized liver. Fenestrations facilitate the transfer of substrates between blood and hepatocytes. With pseudocapillarization of the hepatic sinusoid in old age, there is a loss of fenestrations. LSECs are uniquely exposed to gut-derived dietary and microbial substrates delivered by the portal circulation to the liver. Here we studied the effect of 25 diets varying in content of macronutrients and energy on LSEC fenestrations using the Geometric Framework method in a large cohort of mice aged 15 mo. Macronutrient distribution rather than total food or energy intake was associated with changes in fenestrations. Porosity and frequency were inversely associated with dietary fat intake, while fenestration diameter was inversely associated with protein or carbohydrate intake. Fenestrations were also linked to diet-induced changes in gut microbiome, with increased fenestrations associated with higher abundance of Firmicutes and reduced abundance of Bacteroidetes. Diet-induced changes in levels of several fatty acids (C16:0, C19:0, and C20:4) were also significantly inversely associated with fenestrations, suggesting a link between dietary fat and modulation of lipid rafts in the LSECs. Diet influences fenestrations and these data reflect both the key role of the LSECs in clearing gut-derived molecules from the vascular circulation and the impact these molecules have on LSEC morphology. © 2016 the American Physiological Society.