The effects of protein kinase C (PKC) activation and inhibition on the inositol 1,4,5-trisphosphate (IP 3 ) and cytosolic Ca 2Ο© ([Ca 2Ο© ] i ) responses of rat submandibular acinar cells were investigated. IP 3 formation in response to acetylcholine (ACh) was not affected by the PKC activator phorbol
Role of extracellular Ca2+ in acetylcholine-induced repetitive Ca2+ release in submandibular gland acinar cells of the rat
β Scribed by W. Zhang; Y. Fukushi; A. Nishiyama; J. Wada; N. Kamimura; Y. Mio; M. Wakui
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 859 KB
- Volume
- 167
- Category
- Article
- ISSN
- 0021-9541
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β¦ Synopsis
Acetylcholine (ACh) caused repetitive transient CI-currents activated by intracellular Caz+ in single rat submandibular grand acinar cells. As the concentration of ACh increased the amplitude and the frequency of the transient CI-currents increased. These responses occurred also in the absence of extracellular Caz+ but disappeared after several minutes. Repetitive transient CI-currents were restored by readmission of Ca" to the extracellular solution. The higher the concentration of extracellular Ca2+ readmitted, the larger the amplitude of the transient CI-currents. Caz+ entry through a store-coupled pathway was detected by application of Ca" to the extracellular solution during a brief cessation of stimulation with ACh. In these experiments too, the higher the concentration of Ca2+, the larger the transient CI-currents activated by Ca2+ released from the stores. The time course of decrease in total charge movements of repetitive transient responses to ACh with removal of extracellular Ca2' depended on a decrease in charge movements of each transient event rather than a decrease in frequency of the repetitive events. The decrease of charge movements of each transient event was due to a decrease in its amplitude rather than its duration. The results suggest that in this cell type an amplitude-modulated mechanism is involved in repetitive Ca2+ release and that Ca2+ entry is essential to maintain the repetitive release of Caz+. The results further suggest that the magnitude of Ca2+ entry determines the number of unitary stores filled with Ca2+ which can synchronously respond to ACh.
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## Abstract Uptake of H^3^βleucine into secretory product and its subsequent intracellular transport was analyzed by electron microscopic autoradiographic techniques in the rat submandibular gland acinar cells in vitro. The route and kinetic timetable of intracellular transport was established for