The SCFA butyrate stimulates the epithelial production of retinoic acid via inhibition of epithelial HDAC

• Published in: American journal of physiology: Gastrointestinal and liver physiology Vol. 310; no. 11; pp. G1138 - G1146
• Main Authors: Schilderink, Ronald, Verseijden, Caroline, Seppen, Jurgen, Muncan, Vanesa, van den Brink, Gijs R., Lambers, Tim T., van Tol, Eric A., de Jonge, Wouter J.
• Format: Journal Article
• Language: English
• Published: United States 01.06.2016
• Subjects: Aldehyde Oxidoreductases - genetics; Aldehyde Oxidoreductases - metabolism; Animals; Butyrates - pharmacology; Caco-2 Cells; Cells, Cultured; Histone Deacetylase Inhibitors - pharmacology; Histone Deacetylases - metabolism; Humans; Intestinal Mucosa - drug effects; Intestinal Mucosa - metabolism; Mice; Mice, Inbred C57BL; Microfilament Proteins - genetics; Microfilament Proteins - metabolism; Mucin-2 - genetics; Mucin-2 - metabolism; Tretinoin - metabolism; epithelial cells; immune tolerance; retinoic acid; butyrate; short-chain fatty acids
• ISSN: 0193-1857; 1522-1547; 1522-1547
• DOI: 10.1152/ajpgi.00411.2015

In the intestinal mucosa, retinoic acid (RA) is a critical signaling molecule. RA is derived from dietary vitamin A (retinol) through conversion by aldehyde dehydrogenases (aldh). Reduced levels of short-chain fatty acids (SCFAs) are associated with pathological microbial dysbiosis, inflammatory disease, and allergy. We hypothesized that SCFAs contribute to mucosal homeostasis by enhancing RA production in intestinal epithelia. With the use of human and mouse epithelial cell lines and primary enteroids, we studied the effect of SCFAs on the production of RA. Functional RA conversion was analyzed by Adlefluor activity assays. Butyrate (0–20 mM), in contrast to other SCFAs, dose dependently induced aldh1a1 or aldh1a3 transcript expression and increased RA conversion in human and mouse epithelial cells. Epithelial cell line data were replicated in intestinal organoids. In these organoids, butyrate (2–5 mM) upregulated aldh1a3 expression (36-fold over control), whereas aldh1a1 was not significantly affected. Butyrate enhanced maturation markers ( Mucin-2 and villin) but did not consistently affect stemness markers or other Wnt target genes ( lgr5, olfm4, ascl2, cdkn1). In enteroids, the stimulation of RA production by SCFA was mimicked by inhibitors of histone deacetylase 3 (HDAC3) but not by HDAC1/2 inhibitors nor by agonists of butyrate receptors G-protein-coupled receptor (GPR)43 or GPR109A, indicating that butyrate stimulates RA production via HDAC3 inhibition. We conclude that the SCFA butyrate inhibits HDAC3 and thereby supports epithelial RA production.