{"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}
引用次数: 52
Abstract
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.