Chenodeoxycholic acid requires activation of EGFR, EPAC, and Ca2+ to stimulate CFTR-dependent Cl- secretion in human colonic T84 cells

• Published in: American Journal of Physiology: Cell Physiology 2016-11, Vol.311 (5), p.C777-C792
• Main Authors: Domingue, Jada C, Ao, Mei, Sarathy, Jayashree, Rao, Mrinalini C
• Format: Article
• Language: English
• Subjects: Calcium - metabolism; Cell Line, Tumor; Cell Membrane - metabolism; Chenodeoxycholic Acid - metabolism; Chloride Channels - metabolism; Chlorides - metabolism; Colon - metabolism; Cyclic AMP - metabolism; Cystic Fibrosis Transmembrane Conductance Regulator - metabolism; Epithelial Cells - metabolism; Guanine Nucleotide Exchange Factors - metabolism; Humans; Phosphatidylinositol 3-Kinases - metabolism; Receptor, Epidermal Growth Factor - metabolism; Signal Transduction - physiology
• ISSN: 1522-1563
• DOI: 10.1152/ajpcell.00168.2016

Bile acids are known to initiate intricate signaling events in a variety of tissues, primarily in the liver and gastrointestinal tract. Of the known bile acids, only the 7α-dihydroxy species, deoxycholic acid and chenodeoxycholic acid (CDCA), and their conjugates, activate processes that stimulate epithelial Cl secretion. We have previously published that CDCA acts in a rapid manner to stimulate colonic ion secretion via protein kinase A (PKA)-mediated activation of the dominant Cl channel, the cystic fibrosis transmembrane conductance regulator (CFTR) (Ao M, Sarathy J, Domingue J, Alrefai WA, and Rao MC. Am J Physiol Cell Physiol 305: C447-C456, 2013); however, PKA signaling did not account for the entire CDCA response. Here we show that in human colonic T84 cells, CDCA's induction of CFTR activity, measured as changes in short-circuit current (I ), is dependent on epidermal growth factor receptor (EGFR) activation and does not involve the bile acid receptors TGR5 or farnesoid X receptor. CDCA activation of Cl secretion does not require Src, mitogen-activated protein kinases, or phosphoinositide 3-kinase downstream of EGFR but does require an increase in cytosolic Ca In addition to PKA signaling, we found that the CDCA response requires the novel involvement of the exchange protein directly activated by cAMP (EPAC). EPAC is a known hub for cAMP and Ca cross talk. Downstream of EPAC, CDCA activates Rap2, and changes in free cytosolic Ca were dependent on both EPAC and EGFR activation. This study establishes the complexity of CDCA signaling in the colonic epithelium and shows the contribution of EGFR, EPAC, and Ca in CDCA-induced activation of CFTR-dependent Cl secretion.