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  • Crosstalk between purinergic receptors and canonical signaling pathways in the mouse salivary gland.

Crosstalk between purinergic receptors and canonical signaling pathways in the mouse salivary gland.

Cell calcium (2015-10-08)
Sumit Bhattacharya, John F Imbery, Prince Tuffour Ampem, David R Giovannucci
ZUSAMMENFASSUNG

Isolated clusters of mouse parotid acinar cells in combination with live cell imaging were used to explore the crosstalk in molecular signaling between purinergic, cholinergic and adrenergic pathways that integrate to control fluid and protein secretion. This crosstalk was manifested by (1) β-adrenergic receptor activation and amplification of P2X4R evoked Ca(2+) signals, (2) β-adrenergic-induced amplification of P2X7R-evoked Ca(2+) signals and (3) muscarinic receptor induced activation of P2X7Rs via exocytotic activity. The findings from our study reveal that purinoceptor-mediated Ca(2+) signaling is modulated by crosstalk with canonical signaling pathways in parotid acinar cells. Integration of these signals are likely important for dynamic control of saliva secretion to match physiological demand in the parotid gland.

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Salzsäure, ACS reagent, 37%
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Salzsäure, ACS reagent, 37%
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2-Mercaptoethanol, Molecular Biology, suitable for electrophoresis, suitable for cell culture, BioReagent, 99% (GC/titration)
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3-Isobutyl-1-methylxanthin, ≥99% (HPLC), powder
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2-Mercaptoethanol, ≥99.0%
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Adenosin-5′-triphosphat Dinatriumsalz Hydrat, Grade I, ≥99%, from microbial
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Forskolin, from Coleus forskohlii, ≥98% (HPLC), powder
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Salzsäure, meets analytical specification of Ph. Eur., BP, NF, fuming, 36.5-38%
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3-Isobutyl-1-methylxanthin, BioUltra, ≥99%
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Adenosin-5′-triphosphat Dinatriumsalz Hydrat, BioXtra, ≥99% (HPLC), from microbial
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