Local and global calcium signals and fluid and electrolyte secretion in mouse submandibular acinar cells
Polarized Ca2+ signals that originate at and spread from the apical pole have been shown to occur in acinar cells from lacrimal, parotid, and pancreatic glands. However, "local" Ca2+ signals, that are restricted to the apical pole of the cell, have been previously demonstrated only in panc...
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Veröffentlicht in: | American journal of physiology: Gastrointestinal and liver physiology 2005, Vol.51 (1), p.G118-G124 |
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description | Polarized Ca2+ signals that originate at and spread from the apical pole have been shown to occur in acinar cells from lacrimal, parotid, and pancreatic glands. However, "local" Ca2+ signals, that are restricted to the apical pole of the cell, have been previously demonstrated only in pancreatic acinar cells in which the primary function of the Ca2+ signal is to regulate exocytosis. We show that submandibular acinar cells, in which the primary function of the Ca2+ signal is to drive fluid and electrolyte secretion, are capable of both Ca2+ waves and local Ca2+ signals. The generally accepted model for fluid and electrolyte secretion requires simultaneous Ca2+-activation of basally located K+ channels and apically located Cl- channels. Whereas a propagated cell-wide Ca2+ signal is clearly consistent with this model, a local Ca2+ signal is not, because there is no increase in intracellular Ca2+ concentration at the basal pole of the cell. Our data provide the first direct demonstration, in submandibular acinar cells, of the apical and basal location of the Cl- and K+ channels, respectively, and confirm that local Ca2+ signals do not Ca2+-activate K+ channels. We reevaluate the model for fluid and electrolyte secretion and demonstrate that Ca2+-activation of the Cl- channels is sufficient to voltage-activate the K+ channels and thus demonstrate that local Ca2+ signals are sufficient to support fluid secretion. [PUBLICATION ABSTRACT] |
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R ; SMITH, P. M ; GALLACHER, D. V</creator><creatorcontrib>HARMER, A. R ; SMITH, P. M ; GALLACHER, D. V</creatorcontrib><description>Polarized Ca2+ signals that originate at and spread from the apical pole have been shown to occur in acinar cells from lacrimal, parotid, and pancreatic glands. However, "local" Ca2+ signals, that are restricted to the apical pole of the cell, have been previously demonstrated only in pancreatic acinar cells in which the primary function of the Ca2+ signal is to regulate exocytosis. We show that submandibular acinar cells, in which the primary function of the Ca2+ signal is to drive fluid and electrolyte secretion, are capable of both Ca2+ waves and local Ca2+ signals. The generally accepted model for fluid and electrolyte secretion requires simultaneous Ca2+-activation of basally located K+ channels and apically located Cl- channels. Whereas a propagated cell-wide Ca2+ signal is clearly consistent with this model, a local Ca2+ signal is not, because there is no increase in intracellular Ca2+ concentration at the basal pole of the cell. Our data provide the first direct demonstration, in submandibular acinar cells, of the apical and basal location of the Cl- and K+ channels, respectively, and confirm that local Ca2+ signals do not Ca2+-activate K+ channels. We reevaluate the model for fluid and electrolyte secretion and demonstrate that Ca2+-activation of the Cl- channels is sufficient to voltage-activate the K+ channels and thus demonstrate that local Ca2+ signals are sufficient to support fluid secretion. 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V</creatorcontrib><title>Local and global calcium signals and fluid and electrolyte secretion in mouse submandibular acinar cells</title><title>American journal of physiology: Gastrointestinal and liver physiology</title><description>Polarized Ca2+ signals that originate at and spread from the apical pole have been shown to occur in acinar cells from lacrimal, parotid, and pancreatic glands. However, "local" Ca2+ signals, that are restricted to the apical pole of the cell, have been previously demonstrated only in pancreatic acinar cells in which the primary function of the Ca2+ signal is to regulate exocytosis. We show that submandibular acinar cells, in which the primary function of the Ca2+ signal is to drive fluid and electrolyte secretion, are capable of both Ca2+ waves and local Ca2+ signals. The generally accepted model for fluid and electrolyte secretion requires simultaneous Ca2+-activation of basally located K+ channels and apically located Cl- channels. Whereas a propagated cell-wide Ca2+ signal is clearly consistent with this model, a local Ca2+ signal is not, because there is no increase in intracellular Ca2+ concentration at the basal pole of the cell. Our data provide the first direct demonstration, in submandibular acinar cells, of the apical and basal location of the Cl- and K+ channels, respectively, and confirm that local Ca2+ signals do not Ca2+-activate K+ channels. We reevaluate the model for fluid and electrolyte secretion and demonstrate that Ca2+-activation of the Cl- channels is sufficient to voltage-activate the K+ channels and thus demonstrate that local Ca2+ signals are sufficient to support fluid secretion. [PUBLICATION ABSTRACT]</description><subject>Biological and medical sciences</subject><subject>Calcium</subject><subject>Cells</subject><subject>Electrolytes</subject><subject>Fluids</subject><subject>Fundamental and applied biological sciences. 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We show that submandibular acinar cells, in which the primary function of the Ca2+ signal is to drive fluid and electrolyte secretion, are capable of both Ca2+ waves and local Ca2+ signals. The generally accepted model for fluid and electrolyte secretion requires simultaneous Ca2+-activation of basally located K+ channels and apically located Cl- channels. Whereas a propagated cell-wide Ca2+ signal is clearly consistent with this model, a local Ca2+ signal is not, because there is no increase in intracellular Ca2+ concentration at the basal pole of the cell. Our data provide the first direct demonstration, in submandibular acinar cells, of the apical and basal location of the Cl- and K+ channels, respectively, and confirm that local Ca2+ signals do not Ca2+-activate K+ channels. We reevaluate the model for fluid and electrolyte secretion and demonstrate that Ca2+-activation of the Cl- channels is sufficient to voltage-activate the K+ channels and thus demonstrate that local Ca2+ signals are sufficient to support fluid secretion. [PUBLICATION ABSTRACT]</abstract><cop>Bethesda, MD</cop><pub>American Physiological Society</pub></addata></record> |
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subjects | Biological and medical sciences Calcium Cells Electrolytes Fluids Fundamental and applied biological sciences. Psychology Rodents Vertebrates: digestive system |
title | Local and global calcium signals and fluid and electrolyte secretion in mouse submandibular acinar cells |
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