Guerbette · Frontiers in cell and developmental biology 2024 · In vitro comparative cell culture study · n=?

Saturated fatty acids differently affect mitochondrial function and the intestinal epithelial barrier depending on their chain length in the in vitro model of IPEC-J2 enterocytes.

Cited 28 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

In vitro cell culture study (preclinical model)

PubMed 38362040 · doi:10.3389/fcell.2024.1266842 · record verified 2026-08-31

What was done

Porcine intestinal epithelial cells (IPEC-J2 enterocytes) were treated in vitro for 3 days with 250 µM of four dietary saturated fatty acids: lauric (C12:0), myristic (C14:0), palmitic (C16:0), or stearic (C18:0) acids. Researchers assessed tight junction integrity via transepithelial electrical resistance (TEER), tight junction gene expression, fatty acid β-oxidation, oxidative phosphorylation (OXPHOS) coupling, ATP production, mitochondrial reactive oxygen species (ROS) generation, and mitochondrial network remodeling (fission versus fusion).

What was found

The abstract reports no numerical values. Directionally, only C16:0 and C18:0 increased epithelial permeability without altering tight junction gene expression. C16:0 and C18:0 were barely β-oxidized, significantly uncoupled OXPHOS with increased proton leaks, decreased ATP production, increased mitochondrial ROS, and induced mitochondrial fission. In contrast, C12:0 and C14:0 promoted lipid storage and mitochondrial fusion, caused only mild reductions in ATP production, and did not alter epithelial barrier integrity.

Why it matters

This study shows that the detrimental effects of saturated fatty acids on intestinal epithelial barrier function and mitochondrial bioenergetics are chain-length dependent, specifically occurring with C16:0 and C18:0 but not C12:0 and C14:0.

Limits

The study is restricted to an in vitro porcine cell line exposed to isolated fatty acids at a single concentration (250 µM), lacking in vivo digestive physiology, gut microbiota, and systemic immune interactions. The abstract provides no quantitative data, effect sizes, or experimental replicate counts.

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