ATGL/CGI-58-Dependent Hydrolysis of a Lipid Storage Pool in Murine Enterocytes
Author(s) -
Melanie Korbelius,
Nemanja Vujić,
Vinay Sachdev,
Sascha Obrowsky,
Silvia Rainer,
Benjamin Gottschalk,
Wolfgang F. Graier,
Dagmar Kratky
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.07.030
Subject(s) - chylomicron , adipose triglyceride lipase , lipid droplet , lipid metabolism , catabolism , small intestine , secretion , biochemistry , homeostasis , lipoprotein lipase , chemistry , lipoprotein , enterocyte , microbiology and biotechnology , biology , metabolism , adipose tissue , lipolysis , very low density lipoprotein , cholesterol
As circulating lipid levels are balanced by the rate of lipoprotein release and clearance from the plasma, lipid absorption in the small intestine critically contributes to the maintenance of whole-body lipid homeostasis. Within enterocytes, excessive triglycerides are transiently stored as cytosolic lipid droplets (cLDs), and their mobilization sustains lipid supply during interprandial periods. Using mice lacking adipose triglyceride lipase (ATGL) and its coactivator comparative gene identification-58 (CGI-58) exclusively in the intestine (intestine-specific double KO [iDKO]), we show that ATGL/CGI-58 are not involved in providing substrates for chylomicron synthesis. Massive intestinal cLD accumulation in iDKO mice independent of dietary lipids together with inefficient lipid incorporation into cLDs in the early absorption phase demonstrate the existence of a secretion/re-uptake cycle, corroborating the availability of two diverse cLD pools. This study identified ATGL/CGI-58 as critical players in the catabolism of basolaterally (blood) derived lipids and highlights the necessity to modify the current model of intestinal lipid metabolism.
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