DENND5B Disruption Results in Reduced Body Fat and Increased Intestinal Fatty Acid Oxidation by Activation of Autophagy
Intestinal absorption of dietary lipid is essential for systemic lipid homeostasis; however, elevated postprandial plasma lipid levels are associated with obesity and increased risk for atherosclerotic cardiovascular disease. In humans and rodents, biological sex impacts dietary triglyceride absorption and males tend to have higher postprandial triglyceride levels compared to females, but the physiological basis for this is not well understood. Here, we show that the gene DENND5B is associated with body composition in humans and mice and that genetic deletion of Dennd5b in mice prevents postprandial plasma triglyceride elevations in both sexes. Our findings establish a role for this protein in intestinal chylomicron secretion and reveal a biological sex-biased differential impact of its deletion on body composition, dietary fatty acid uptake, and intestinal metabolism. Mechanistically, our findings implicate autophagy and mitochondrial beta oxidation in coping with enterocyte lipid accumulation due to impaired chylomicron secretion. This work extends the emerging concept that the intestinal epithelium may play a prominent role in oxidation of diet-derived fatty acids and suggests that this process may contribute to biological sex-based differences in postprandial lipemia and body composition.
Authors
- Karen Reue (ORCID: https://orcid.org/0000-0002-7487-2624)
- Maura Mobilia
- Alexander Karakashian
- Khaga R. Neupane
- Laurent Vergnes (ORCID: https://orcid.org/0000-0002-8804-589X)
- Min Liu (ORCID: https://orcid.org/0000-0003-2505-0218)
- Olivia Hage
- Patrick Tso
Institutions
- University of Kentucky (US)
- University of California, Los Angeles (US)
- University of Cincinnati (US)
Publication Details
- Journal
- Journal of Lipid Research
- Published
- 2026-04-01
- DOI
- https://doi.org/10.1016/j.jlr.2026.101037
- Primary Topic
- Body Contouring and Surgery
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- American Heart Association
- National Institute of General Medical Sciences
- National Institute of Diabetes and Digestive and Kidney Diseases