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Using Caco-2 Cells to Study Lipid Transport by the Intestine
Published on: August 20, 2015
Enteroendocrine cells and lipid absorption.
Georg Mellitzer1, Gerard Gradwohl
1Institut de Génétique et de Biologie Moléculaire et Cellulaire, INSERM U964, CNRS UMR 7104, Université de Strasbourg, Illkirch, France. mellit@igbmc.fr
Current Opinion in Lipidology
|April 6, 2011
Summary
Enteroendocrine cells, crucial for nutrient sensing, significantly impact lipid absorption. Their hormones regulate chylomicron formation, offering new therapeutic targets for metabolic disorders like obesity.
Area of Science:
- Gastroenterology
- Endocrinology
- Cell Biology
Background:
- Enteroendocrine cells (EECs) are specialized cells in the gut epithelium.
- EECs secrete hormones that regulate various physiological functions, including appetite and glucose homeostasis.
Purpose of the Study:
- To review recent literature on the role of enteroendocrine cells in lipid absorption.
- To explore the mechanisms by which EECs influence dietary fat uptake and processing.
Main Methods:
- Analysis of studies involving genetic manipulation of enteroendocrine cell development (e.g., Ngn3 inactivation).
- Review of gain and loss of function experiments in animal models (mouse, hamster) and primary enterocytes.
- Examination of the role of specific molecules like apoB-48 and CD36 in EEC-mediated lipid absorption.
Main Results:
- Inactivation of neurogenin 3 (Ngn3) in intestinal EECs results in impaired lipid absorption and growth retardation.
- Enteroendocrine hormones regulate the formation and secretion of apoB-48-containing chylomicrons.
- The scavenger receptor CD36's glycosylation is indirectly stimulated by EECs, influencing lipid handling.
Conclusions:
- Enteroendocrine cells play a significant, previously underappreciated role in regulating lipid absorption.
- EEC-derived hormones influence key pathways in dietary fat metabolism, including chylomicron assembly.
- These findings highlight EECs as potential therapeutic targets for obesity and related metabolic disorders.
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