» Articles » PMID: 2388255

Lowering Extracellular Sodium or PH Raises Intracellular Calcium in Gastric Cells

Overview
Journal J Membr Biol
Date 1990 Jul 1
PMID 2388255
Citations 11
Authors
Affiliations
Soon will be listed here.
Abstract

The dependence of cytoplasmic free [Ca] (Cai) on [Na] and pH was assessed in individual parietal cells of intact rabbit gastric glands by microfluorimetry of fura-2. Lowering extracellular [Na] (Nao) to 20 mM or below caused a biphasic Cai increase which consisted of both release of intracellular Ca stores and Ca entry across the plasma membrane. The Ca increase was not blocked by antagonists of Ca-mobilizing receptors (atropine or cimetidine) and was independent of the replacement cation. Experiments in Ca-free media and in Na-depleted cells indicated that neither phase was due to reversal of Na/Ca exchange. The steep dependence of the Cai increase on Nao suggested that the response was not due to lowering intracellular [Na] (Nai). The effects of low Nao on Cai were also completely independent of changes in intracellular pH (pHi). Cai was remarkably stable during changes of pHi of up to 2 pH units, indicating that H and Ca do not share a cytoplasmic buffer system. Such large pH excursions required determination of the pH dependence of fura-2. Because fura-2 was found to decrease its affinity for Ca as pH decreased below 6.7, corrections were applied to experiments in which large pHi changes were observed. In contrast to the relative insensitivity of Cai to changes in pHi, decreasing extracellular pH (pHo) to 6.0 or below was found to stimulate release of intracellular Ca stores. Increased Ca entry was not observed in this case. The ability of decreases in Nao and pHo to stimulate release of intracellular Ca stores suggest interactions between Na and H with extracellular receptors.

Citing Articles

The Roles of Proton-Sensing G-Protein-Coupled Receptors in Inflammation and Cancer.

Justus C, Marie M, Sanderlin E, Yang L Genes (Basel). 2024; 15(9).

PMID: 39336742 PMC: 11431078. DOI: 10.3390/genes15091151.


Extracellular HCO3- is sensed by mouse cerebral arteries: Regulation of tone by receptor protein tyrosine phosphatase γ.

Boedtkjer E, Hansen K, Boedtkjer D, Aalkjaer C, Boron W J Cereb Blood Flow Metab. 2015; 36(5):965-80.

PMID: 26661205 PMC: 4853837. DOI: 10.1177/0271678X15610787.


Extracellular H+ induces Ca2+ signals in respiratory chemoreceptors of zebrafish.

Abdallah S, Jonz M, Perry S Pflugers Arch. 2014; 467(2):399-413.

PMID: 24770973 DOI: 10.1007/s00424-014-1514-2.


Intracellular pH modulates inner segment calcium homeostasis in vertebrate photoreceptors.

Krizaj D, Mercer A, Thoreson W, Barabas P Am J Physiol Cell Physiol. 2010; 300(1):C187-97.

PMID: 20881233 PMC: 3023182. DOI: 10.1152/ajpcell.00264.2010.


Dynamic but not constitutive association of calmodulin with rat TRPV6 channels enables fine tuning of Ca2+-dependent inactivation.

Derler I, Hofbauer M, Kahr H, Fritsch R, Muik M, Kepplinger K J Physiol. 2006; 577(Pt 1):31-44.

PMID: 16959851 PMC: 2000671. DOI: 10.1113/jphysiol.2006.118661.


References
1.
Nasmith P, Grinstein S . Phorbol ester-induced changes in cytoplasmic Ca2+ in human neutrophils. Involvement of a pertussis toxin-sensitive G protein. J Biol Chem. 1987; 262(28):13558-66. View

2.
Smith J, Dwyer S, Smith L . Lowering extracellular pH evokes inositol polyphosphate formation and calcium mobilization. J Biol Chem. 1989; 264(15):8723-8. View

3.
Chew C . Cholecystokinin, carbachol, gastrin, histamine, and forskolin increase [Ca2+]i in gastric glands. Am J Physiol. 1986; 250(6 Pt 1):G814-23. DOI: 10.1152/ajpgi.1986.250.6.G814. View

4.
Siskind M, McCoy C, Chobanian A, Schwartz J . Regulation of intracellular calcium by cell pH in vascular smooth muscle cells. Am J Physiol. 1989; 256(2 Pt 1):C234-40. DOI: 10.1152/ajpcell.1989.256.2.C234. View

5.
Mullins L, Requena J . Calcium measurement in the periphery of an axon. J Gen Physiol. 1979; 74(3):393-413. PMC: 2228528. DOI: 10.1085/jgp.74.3.393. View