{"title":"Homer2通过小鼠腮腺腺泡细胞的生理钙振荡调节淀粉酶分泌","authors":"Namju Kang, J. Y. Kang, D. Shin, Yu-Mi Yang","doi":"10.11620/ijob.2020.45.2.58","DOIUrl":null,"url":null,"abstract":"The salivary glands secrete saliva, which plays a role in the maintenance of a healthy oral environment. Under physiological conditions, saliva secretion within the acinar cells of the gland is regulated by stimulation of specific calcium (Ca 2+ ) signaling mechanisms such as increases in the intracellular Ca 2+ concentration ([Ca 2+ ] i ) via store-operated Ca 2+ entry, which involves components such as Orai1, transient receptor potential (TRP) canonical 1, stromal interaction molecules, and inositol 1,4,5-triphosphate (IP 3 ) receptors (IP 3 Rs). Homer proteins are scaffold proteins that bind to G protein-coupled receptors, IP 3 Rs, ryanodine receptors, and TRP channels. However, their exact role in Ca 2+ signaling in the salivary glands remains unknown. In the present study, we investigated the role of Homer2 in Ca 2+ signaling and saliva secretion in parotid gland acinar cells under physiological conditions. Deletion of Homer2 (Homer2 −/− ) markedly decreased the amplitude of [Ca 2+ ] i oscillations via the stimulation of carbachol, which is physiologically concentrated in parotid acinar cells, whereas the frequency of [Ca 2+ ] i oscillations showed no difference between wild-type and Homer2 −/− mice. Homer2 −/− mice also showed a significant decrease in amylase release by carbachol in the parotid gland in a dose-dependent manner. These results suggest that Homer2 plays a critical role in maintaining [Ca 2+ ] i concentration and secretion of saliva in mouse parotid gland acinar cells.","PeriodicalId":14180,"journal":{"name":"International Journal of Oral Biology","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Homer2 regulates amylase secretion via physiological calcium oscillations in mouse parotid gland acinar cells\",\"authors\":\"Namju Kang, J. Y. Kang, D. Shin, Yu-Mi Yang\",\"doi\":\"10.11620/ijob.2020.45.2.58\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The salivary glands secrete saliva, which plays a role in the maintenance of a healthy oral environment. Under physiological conditions, saliva secretion within the acinar cells of the gland is regulated by stimulation of specific calcium (Ca 2+ ) signaling mechanisms such as increases in the intracellular Ca 2+ concentration ([Ca 2+ ] i ) via store-operated Ca 2+ entry, which involves components such as Orai1, transient receptor potential (TRP) canonical 1, stromal interaction molecules, and inositol 1,4,5-triphosphate (IP 3 ) receptors (IP 3 Rs). Homer proteins are scaffold proteins that bind to G protein-coupled receptors, IP 3 Rs, ryanodine receptors, and TRP channels. However, their exact role in Ca 2+ signaling in the salivary glands remains unknown. In the present study, we investigated the role of Homer2 in Ca 2+ signaling and saliva secretion in parotid gland acinar cells under physiological conditions. Deletion of Homer2 (Homer2 −/− ) markedly decreased the amplitude of [Ca 2+ ] i oscillations via the stimulation of carbachol, which is physiologically concentrated in parotid acinar cells, whereas the frequency of [Ca 2+ ] i oscillations showed no difference between wild-type and Homer2 −/− mice. Homer2 −/− mice also showed a significant decrease in amylase release by carbachol in the parotid gland in a dose-dependent manner. These results suggest that Homer2 plays a critical role in maintaining [Ca 2+ ] i concentration and secretion of saliva in mouse parotid gland acinar cells.\",\"PeriodicalId\":14180,\"journal\":{\"name\":\"International Journal of Oral Biology\",\"volume\":\"13 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Oral Biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.11620/ijob.2020.45.2.58\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Oral Biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.11620/ijob.2020.45.2.58","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Homer2 regulates amylase secretion via physiological calcium oscillations in mouse parotid gland acinar cells
The salivary glands secrete saliva, which plays a role in the maintenance of a healthy oral environment. Under physiological conditions, saliva secretion within the acinar cells of the gland is regulated by stimulation of specific calcium (Ca 2+ ) signaling mechanisms such as increases in the intracellular Ca 2+ concentration ([Ca 2+ ] i ) via store-operated Ca 2+ entry, which involves components such as Orai1, transient receptor potential (TRP) canonical 1, stromal interaction molecules, and inositol 1,4,5-triphosphate (IP 3 ) receptors (IP 3 Rs). Homer proteins are scaffold proteins that bind to G protein-coupled receptors, IP 3 Rs, ryanodine receptors, and TRP channels. However, their exact role in Ca 2+ signaling in the salivary glands remains unknown. In the present study, we investigated the role of Homer2 in Ca 2+ signaling and saliva secretion in parotid gland acinar cells under physiological conditions. Deletion of Homer2 (Homer2 −/− ) markedly decreased the amplitude of [Ca 2+ ] i oscillations via the stimulation of carbachol, which is physiologically concentrated in parotid acinar cells, whereas the frequency of [Ca 2+ ] i oscillations showed no difference between wild-type and Homer2 −/− mice. Homer2 −/− mice also showed a significant decrease in amylase release by carbachol in the parotid gland in a dose-dependent manner. These results suggest that Homer2 plays a critical role in maintaining [Ca 2+ ] i concentration and secretion of saliva in mouse parotid gland acinar cells.