![]()
|
|
||||||||
J. Biol. Chem., Vol. 262, Issue 11, 4958-4960, 04, 1987
JE Merritt and TJ Rink
Carbachol-evoked rises in [Ca2+]i were measured in fura-2-loaded, rat parotid acinar cells. In suspensions of dissociated cells examined by dual wavelength excitation fluorimetry, a maximally effective concentration of carbachol produced a measured peak [Ca2+]i of 780 +/- 60 nM followed by a maintained elevation in the presence of 1 mM external Ca2+, and a peak of 630 +/- 95 nM followed by a return to resting values in the absence of external Ca2+. Stopped-flow, single wavelength fluorimetry was used to resolve the rising phase of the response. There was a dose-dependent lag of 70-220 ms before [Ca2+]i started to increase, and [Ca2+]i was maximal by 800-900 ms. These times were similar in the presence or absence of external Ca2+, although the initial rate of rise was faster in the presence of external Ca2+. These kinetics are consistent with a biochemical event, possibly phosphatidylinositol bisphosphate hydrolysis, mediating both internal release and Ca2+ entry, with a component of the initial rise being due to Ca2+ entry.
This article has been cited by other articles:
![]() |
Y. Ma, E. Kobrinsky, and A. R. Marks Cloning and Expression of a Novel Truncated Calcium Channel from Non-excitable Cells J. Biol. Chem., January 6, 1995; 270(1): 483 - 493. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Foskett and J. Melvin Activation of salivary secretion: coupling of cell volume and [Ca2+]i in single cells Science, June 30, 1989; 244(4912): 1582 - 1585. [Abstract] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| All ASBMB Journals | Molecular and Cellular Proteomics |
| Journal of Lipid Research | ASBMB Today |