{"title":"通过IP(3)受体在HeLa细胞中的高度热敏钙动力学。","authors":"Vadim Tseeb, Madoka Suzuki, Kotaro Oyama, Kaoru Iwai, Shin'ichi Ishiwata","doi":"10.2976/1.3073779","DOIUrl":null,"url":null,"abstract":"<p><p>Intracellular Ca(2+) distribution and its dynamics are essential for various cellular functions. We show with single HeLa cells that a microscopic heat pulse induces Ca(2+) uptake into intracellular stores during heating and Ca(2+) release from them at the onset of recooling, and the overshoot of Ca(2+) release occurs above the critical value of a temperature change, which decreases from 1.5 to 0.2 degrees C on increasing the experimental temperature from 22 to 37 degrees C. This highly thermosensitive Ca(2+) dynamics is probably attributable to the altered balance between Ca(2+) uptake by endoplasmic reticulum Ca(2+)-ATPases and Ca(2+) release via inositol 1,4,5-trisphosphate receptors. These results suggest that Ca(2+) signaling is extremely sensitive to temperature changes, especially around body temperature, in cells expressing inositol 1,4,5-trisphosphate receptors.</p>","PeriodicalId":55056,"journal":{"name":"Hfsp Journal","volume":"3 2","pages":"117-23"},"PeriodicalIF":0.0000,"publicationDate":"2009-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2976/1.3073779","citationCount":"52","resultStr":"{\"title\":\"Highly thermosensitive Ca dynamics in a HeLa cell through IP(3) receptors.\",\"authors\":\"Vadim Tseeb, Madoka Suzuki, Kotaro Oyama, Kaoru Iwai, Shin'ichi Ishiwata\",\"doi\":\"10.2976/1.3073779\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Intracellular Ca(2+) distribution and its dynamics are essential for various cellular functions. We show with single HeLa cells that a microscopic heat pulse induces Ca(2+) uptake into intracellular stores during heating and Ca(2+) release from them at the onset of recooling, and the overshoot of Ca(2+) release occurs above the critical value of a temperature change, which decreases from 1.5 to 0.2 degrees C on increasing the experimental temperature from 22 to 37 degrees C. This highly thermosensitive Ca(2+) dynamics is probably attributable to the altered balance between Ca(2+) uptake by endoplasmic reticulum Ca(2+)-ATPases and Ca(2+) release via inositol 1,4,5-trisphosphate receptors. These results suggest that Ca(2+) signaling is extremely sensitive to temperature changes, especially around body temperature, in cells expressing inositol 1,4,5-trisphosphate receptors.</p>\",\"PeriodicalId\":55056,\"journal\":{\"name\":\"Hfsp Journal\",\"volume\":\"3 2\",\"pages\":\"117-23\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.2976/1.3073779\",\"citationCount\":\"52\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Hfsp Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2976/1.3073779\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2009/3/4 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hfsp Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2976/1.3073779","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2009/3/4 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Highly thermosensitive Ca dynamics in a HeLa cell through IP(3) receptors.
Intracellular Ca(2+) distribution and its dynamics are essential for various cellular functions. We show with single HeLa cells that a microscopic heat pulse induces Ca(2+) uptake into intracellular stores during heating and Ca(2+) release from them at the onset of recooling, and the overshoot of Ca(2+) release occurs above the critical value of a temperature change, which decreases from 1.5 to 0.2 degrees C on increasing the experimental temperature from 22 to 37 degrees C. This highly thermosensitive Ca(2+) dynamics is probably attributable to the altered balance between Ca(2+) uptake by endoplasmic reticulum Ca(2+)-ATPases and Ca(2+) release via inositol 1,4,5-trisphosphate receptors. These results suggest that Ca(2+) signaling is extremely sensitive to temperature changes, especially around body temperature, in cells expressing inositol 1,4,5-trisphosphate receptors.