Intestinal and peritoneal mast cells differ in kinetics of quantal release

• Published in: Biochemical and biophysical research communications Vol. 469; no. 15; pp. 559 - 564
• Main Authors: Balseiro-Gomez, Santiago, M. Pilar Ramirez-Ponce, Jorge Acosta, Eva Ales, Juan A. Flores
• Format: Journal Article
• Language: English
• Published: Elsevier Inc 2016
• Subjects: 5-HT; Amperometry; chondroitin sulfate; CTMC; exocytosis; functional properties; heparin; Ifoot; Imax; IMC; Mast cells; MMC; PMC; proteoglycans; Proteoglycans and serotonin; Qfoot; rats; Risem; secretion; secretory granules; serotonin; t1/2; tfoot
• ISSN: 0006-291X; 1090-2104

5-hydroxytriptamine (5-HT, serotonin) storage and release in mast cell (MC) secretory granules (SG) are dependent on serglycin proteoglycans (PG). This notion is based on the studies of MC of the connective tissue subtype that predominantly contain PG of the heparin type, whereas intestinal mucosal MC, which contain predominantly chondroitin sulfate, have been poorly explored. In the present study, we addressed the possibility that PG contents may differently affect the storage and release of preformed mediators in these two MC subclasses and explain in part their different functional properties. Rat peritoneal (PMC) and intestinal mast cells (IMC) were isolated and purified using a percoll gradient, and the efflux of 5-HT from each SG was measured by amperometric detection. IMC exhibited a ∼34% reduction in the release of 5-HT compared with PMC because of a lower number of exocytotic events, rather than a lower secretion per single exocytotic event. Amperometric spikes from IMC exhibited a slower decay phase and increased half-width but a similar ascending phase and foot parameters, indicating that the fusion pore kinetics are comparable in both MC subclasses. We conclude that both PG subtypes are equally efficient systems, directly involved in serotonin accumulation, and play a crucial role in regulating the kinetics of exocytosis from SG, providing specific secretory properties for the two cellular subtypes.