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Niflumic acid inhibits ATP-stimulated exocytosis in a mucin-secreting epithelial cell line

Authors :
Bertrand, C.A.
Danahay, H.
Poll, C.T.
Laboisse, C.
Hopfer, U.
Bridges, R.J.
Source :
The American Journal of Physiology. Feb, 2004, Vol. 286 Issue 2, pC247, 9 p.
Publication Year :
2004

Abstract

ATP is an efficacious secretagogue for mucin and chloride in the epithelial cell line HT29-C1.16E. Mucin release has been measured as [[sup.3]H]glucosamine-labeled product in extracellular medium and as single-cell membrane capacitance increases indicative of exocytosis-related increases in membrane area. The calcium-activated chloride channel blocker niflumic acid, also reported to modulate secretion, was used to probe for divergence in the purinergic signaling of mucin exocytosis and channel activation. With the use of whole cell patch clamping, ATP stimulated a transient capacitance increase of 15 [+ or -] 4%. Inclusion of niflumic acid significantly reduced the ATP-stimulated capacitance change to 3 [+ or -] 1%, although normalized peak currents were not significantly different. Ratiometric imaging was used to assess intracellular calcium ([Ca.sup.2+.sub.i]) dynamics during stimulation. In the presence of niflumic acid, the ATP-stimulated peak change in [Ca.sup.2+.sub.i] was unaffected, but the initial response and overall time to [Ca.sup.2+.sub.i] peak were significantly affected. Excluding external calcium before ATP stimulation or including the capacitative calcium entry blocker La[Cl.sub.3] during stimulation muted the initial calcium transient similar to that observed with niflumic acid and significantly reduced peak capacitance change, suggesting that a substantial portion of the ATP-stimulated mucin exocytosis in HT29-C1.16E depends on a rapid, brief calcium influx through the plasma membrane. Niflumic acid interferes with this influx independent of a chloride channel blockade effect. capacitative calcium entry; membrane capacitance; chloride channels; fura 2

Details

Language :
English
ISSN :
00029513
Volume :
286
Issue :
2
Database :
Gale General OneFile
Journal :
The American Journal of Physiology
Publication Type :
Academic Journal
Accession number :
edsgcl.114003998