Preclinical knockout study reveals dispensability of intestinal propionate metabolism in mice, suggesting hepatic capture controls systemic physiology.
Propionate is an abundant short-chain fatty acid largely derived from gut microbiota in mammals. Propionate metabolism is essential to maintain systemic homeostasis and inborn errors of essential metabolic enzymes in this pathway cause severe illness. The juxtaposition of high concentrations of propionate with the intestinal epithelium suggests a need for propionate catabolism. To understand the requirement of propionate metabolism in intestinal epithelium, we generated mice with a conditional knockout of Propionyl-CoA Carboxylase A (Pcca) specifically in the intestine (Pcca Vil-Cre ). Male and female Pcca Vil-Cre mice were born and weaned at the expected Mendelian ratio and gained weight normally on chow and high fat diets. Liver metabolomics of Pcca Vil-Cre mice suggest that propionate metabolism affects the gut liver axis. However, the loss of Pcca in the intestine did not affect the colonic transcriptome. These data suggest that intestinal propionate metabolism is largely dispensable, and hepatic capture and metabolism of propionate dominates systemic physiology.
No takes yet. Share an insight, caveat, or question.
Encarnacion et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: