The extracellular calcium-sensing receptor is required for cholecystokinin secretion in response to L-phenylalanine in acutely isolated intestinal I cells

• Published in: American journal of physiology: Gastrointestinal and liver physiology 2011-04, Vol.300 (4), p.G538-G546
• Main Authors: Liou, Alice P, Sei, Yoshitatsu, Zhao, Xilin, Feng, Jianying, Lu, Xinping, Thomas, Craig, Pechhold, Susanne, Raybould, Helen E, Wank, Stephen A
• Format: Article
• Language: English
• Subjects: Amino acids; Animals; Calcium - metabolism; Cells; Cells, Cultured; Cholecystokinin - secretion; Duodenum - cytology; Duodenum - metabolism; Duodenum - secretion; Fluorescent Antibody Technique; Gallbladder diseases; Gene expression; Hormones; Hormones and Signaling; Mice; Mice, Transgenic; Phenylalanine - metabolism; Phenylalanine - pharmacology; Physiology; Proteins; Receptors, Calcium-Sensing - genetics; Receptors, Calcium-Sensing - metabolism; Reverse Transcriptase Polymerase Chain Reaction; Rodents
• ISSN: 0193-1857; 1522-1547
• DOI: 10.1152/ajpgi.00342.2010

The extracellular calcium-sensing receptor (CaSR) has recently been recognized as an L-amino acid sensor and has been implicated in mediating cholecystokinin (CCK) secretion in response to aromatic amino acids. We investigated whether direct detection of L-phenylalanine (L-Phe) by CaSR results in CCK secretion in the native I cell. Fluorescence-activated cell sorting of duodenal I cells from CCK-enhanced green fluorescent protein (eGFP) transgenic mice demonstrated CaSR gene expression. Immunostaining of fixed and fresh duodenal tissue sections confirmed CaSR protein expression. Intracellular calcium fluxes were CaSR dependent, stereoselective for L-Phe over D-Phe, and responsive to type II calcimimetic cinacalcet in CCK-eGFP cells. Additionally, CCK secretion by an isolated I cell population was increased by 30 and 62% in response to L-Phe in the presence of physiological (1.26 mM) and superphysiological (2.5 mM) extracellular calcium concentrations, respectively. While the deletion of CaSR from CCK-eGFP cells did not affect basal CCK secretion, the effect of L-Phe or cinacalcet on intracellular calcium flux was lost. In fact, both secretagogues, as well as superphysiological Ca(2+), evoked an unexpected 20-30% decrease in CCK secretion compared with basal secretion in CaSR(-/-) CCK-eGFP cells. CCK secretion in response to KCl or tryptone was unaffected by the absence of CaSR. The present data suggest that CaSR is required for hormone secretion in the specific response to L-Phe by the native I cell, and that a receptor-mediated mechanism may inhibit hormone secretion in the absence of a fully functional CaSR.