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Enterocyte-specific ATGL overexpression affects intestinal and systemic cholesterol homeostasis

Korbelius, Melanie ; Vujić, Nemanja ; Kuentzel, Katharina B. LU orcid ; Obrowsky, Sascha ; Rainer, Silvia ; Haemmerle, Guenter ; Rülicke, Thomas and Kratky, Dagmar (2022) In Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids 1867(4).
Abstract

Enterocytes of the small intestine (SI) play an important role in maintaining systemic lipid levels by regulating dietary lipid absorption and postprandial lipoprotein secretion. An excessive amount of dietary-derived triglycerides (TGs) taken up by the apical side of enterocytes or basolaterally internalized lipoprotein remnants can be transiently stored in cytosolic lipid droplets (cLDs). As mice lacking adipose TG lipase (ATGL) in the SI display massive accumulation of cLDs but also delayed cholesterol absorption, we hypothesized that SI-specific overexpression of ATGL (Atgl iTg) might have beneficial effects on lipid homeostasis in the gut and possibly throughout the body. Here, we demonstrate that Atgl iTg mice had only modestly... (More)

Enterocytes of the small intestine (SI) play an important role in maintaining systemic lipid levels by regulating dietary lipid absorption and postprandial lipoprotein secretion. An excessive amount of dietary-derived triglycerides (TGs) taken up by the apical side of enterocytes or basolaterally internalized lipoprotein remnants can be transiently stored in cytosolic lipid droplets (cLDs). As mice lacking adipose TG lipase (ATGL) in the SI display massive accumulation of cLDs but also delayed cholesterol absorption, we hypothesized that SI-specific overexpression of ATGL (Atgl iTg) might have beneficial effects on lipid homeostasis in the gut and possibly throughout the body. Here, we demonstrate that Atgl iTg mice had only modestly increased enzymatic activity despite drastically elevated Atgl mRNA levels (up to 120-fold) on chow diet, and was highly induced upon high-fat/high-cholesterol diet (HF/HCD) feeding. Atgl iTg mice showed markedly reduced intestinal TG concentrations after acute and chronic lipid challenge without affecting chylomicron TG secretion. Circulating plasma cholesterol levels were significantly lower in Atgl iTg mice under different feeding conditions, contrasting the accelerated uptake of dietary cholesterol into the circulation after HF/HCD feeding. In the fasted state, gene expression analysis revealed modulation of PPARα and liver X receptor (LXR) target genes by an increased fatty acid release, whereas the decreased plasma cholesterol concentrations in refed mice were more likely due to changes in HDL synthesis and secretion. We conclude that ATGL, in addition to its role in TG catabolism, plays a critical role in whole-body cholesterol homeostasis by modulating PPARα and LXR signaling in intestinal enterocytes.

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author
; ; ; ; ; ; and
publishing date
type
Contribution to journal
publication status
published
keywords
Acyltransferases/genetics, Animals, Cholesterol/metabolism, Enterocytes/metabolism, Homeostasis, Lipase/metabolism, Liver X Receptors/metabolism, Mice, PPAR alpha/metabolism, Triglycerides/metabolism
in
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids
volume
1867
issue
4
article number
159121
publisher
Elsevier
external identifiers
  • scopus:85124324911
  • pmid:35150895
ISSN
1388-1981
DOI
10.1016/j.bbalip.2022.159121
language
English
LU publication?
no
additional info
Copyright © 2021. Published by Elsevier B.V.
id
e755860e-ca06-4761-9e6c-6f4bec7ed6e9
date added to LUP
2022-10-10 16:28:45
date last changed
2024-04-18 09:27:01
@article{e755860e-ca06-4761-9e6c-6f4bec7ed6e9,
  abstract     = {{<p>Enterocytes of the small intestine (SI) play an important role in maintaining systemic lipid levels by regulating dietary lipid absorption and postprandial lipoprotein secretion. An excessive amount of dietary-derived triglycerides (TGs) taken up by the apical side of enterocytes or basolaterally internalized lipoprotein remnants can be transiently stored in cytosolic lipid droplets (cLDs). As mice lacking adipose TG lipase (ATGL) in the SI display massive accumulation of cLDs but also delayed cholesterol absorption, we hypothesized that SI-specific overexpression of ATGL (Atgl iTg) might have beneficial effects on lipid homeostasis in the gut and possibly throughout the body. Here, we demonstrate that Atgl iTg mice had only modestly increased enzymatic activity despite drastically elevated Atgl mRNA levels (up to 120-fold) on chow diet, and was highly induced upon high-fat/high-cholesterol diet (HF/HCD) feeding. Atgl iTg mice showed markedly reduced intestinal TG concentrations after acute and chronic lipid challenge without affecting chylomicron TG secretion. Circulating plasma cholesterol levels were significantly lower in Atgl iTg mice under different feeding conditions, contrasting the accelerated uptake of dietary cholesterol into the circulation after HF/HCD feeding. In the fasted state, gene expression analysis revealed modulation of PPARα and liver X receptor (LXR) target genes by an increased fatty acid release, whereas the decreased plasma cholesterol concentrations in refed mice were more likely due to changes in HDL synthesis and secretion. We conclude that ATGL, in addition to its role in TG catabolism, plays a critical role in whole-body cholesterol homeostasis by modulating PPARα and LXR signaling in intestinal enterocytes.</p>}},
  author       = {{Korbelius, Melanie and Vujić, Nemanja and Kuentzel, Katharina B. and Obrowsky, Sascha and Rainer, Silvia and Haemmerle, Guenter and Rülicke, Thomas and Kratky, Dagmar}},
  issn         = {{1388-1981}},
  keywords     = {{Acyltransferases/genetics; Animals; Cholesterol/metabolism; Enterocytes/metabolism; Homeostasis; Lipase/metabolism; Liver X Receptors/metabolism; Mice; PPAR alpha/metabolism; Triglycerides/metabolism}},
  language     = {{eng}},
  number       = {{4}},
  publisher    = {{Elsevier}},
  series       = {{Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids}},
  title        = {{Enterocyte-specific ATGL overexpression affects intestinal and systemic cholesterol homeostasis}},
  url          = {{http://dx.doi.org/10.1016/j.bbalip.2022.159121}},
  doi          = {{10.1016/j.bbalip.2022.159121}},
  volume       = {{1867}},
  year         = {{2022}},
}