کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
10815737 | 1058500 | 2010 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Enhanced Ca2+ storage in sphingosine-1-phosphate lyase-deficient fibroblasts
دانلود مقاله + سفارش ترجمه
دانلود مقاله ISI انگلیسی
رایگان برای ایرانیان
کلمات کلیدی
Sarco-endoplasmic reticulum Ca2+-ATPaseECFPHBSSIP3MEFsSphKLPAS1PBSA - BSAinositol-1,4,5-trisphosphate - inositol-1،4،5-trisphosphate[Ca2+]i - [Ca2 +] ibovine serum albumin - آلبومین سرم گاوSphingosine kinase - اسپینوزین کینازSphingosine-1-phosphate lyase - اسپینوزین-1 فسفات لیائازSphingosine-1-phosphate - اسپینگسین-1-فسفاتlysophosphatidic acid - اسید لیسفسفیدیدenhanced cyan fluorescent protein - افزایش پروتئین فلورسنت سیانوژنFluorescence resonance energy transfer - انتقال انرژی رزونانس FluorescenceFRET - انتقال انرژی رزونانسی فورسترCalcium signalling - سیگنالینگ کلسیمintracellular free Ca2+ concentration - غلظت Ca2 + آزاد داخل سلولیCalcium stores - فروشگاه های کلسیمSERCA - قلبHank's balanced salt solution - محلول نمک متعادل هانکmouse embryonic fibroblasts - موش فیبروبلاست جنینی
موضوعات مرتبط
علوم زیستی و بیوفناوری
بیوشیمی، ژنتیک و زیست شناسی مولکولی
زیست شیمی
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Enhanced Ca2+ storage in sphingosine-1-phosphate lyase-deficient fibroblasts Enhanced Ca2+ storage in sphingosine-1-phosphate lyase-deficient fibroblasts](/preview/png/10815737.png)
چکیده انگلیسی
Sphingosine-1-phosphate (S1P) regulates cell growth and survival, migration and adhesion in many cell types. S1P is generated by sphingosine kinases (SphKs), and dephosphorylated by phosphatases or cleaved by S1P lyase. Extracellular S1P activates specific G protein-coupled receptors while intracellular S1P can mobilize Ca2+ from thapsigargin-sensitive stores. Here, we have studied Ca2+ signalling in mouse embryonic fibroblasts (MEFs) deficient in S1P lyase. In these cells, S1P and sphingosine concentrations were elevated about 6-fold and 2-fold, respectively, as measured by liquid chromatography/tandem mass spectrometry. Measurements with fura-2-loaded cells in suspension revealed that resting [Ca2+]i was elevated and agonist-induced [Ca2+]i increases were augmented in S1P lyase-deficient MEFs both in the presence and absence of extracellular Ca2+. Importantly, [Ca2+]i increases and Ca2+ mobilization induced by the SERCA inhibitor, thapsigargin, were augmented, indicating enhanced Ca2+ storage in S1P lyase-deficient MEFs. Measurements with single cells expressing the calmodulin-based Ca2+ sensor, cameleon, revealed that at least two cell types could be distinguished in both MEF cell populations, one with a rapid and transient [Ca2+]i increase and the other with a slower and prolonged [Ca2+]i elevation upon stimulation with thapsigargin. The area under the time course of thapsigargin-induced [Ca2+]i increases, reflecting overall Ca2+ release, was significantly increased by more than 50% in both rapidly and slowly responding S1P lyase-deficient cells. It is concluded that elevated concentrations of S1P and/or sphingosine lead to enhanced Ca2+ storage and elevated basal [Ca2+]i. S1P metabolism thus plays a role not only in acute Ca2+ mobilization but also in long-term regulation of Ca2+ homeostasis.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Cellular Signalling - Volume 22, Issue 3, March 2010, Pages 476-483
Journal: Cellular Signalling - Volume 22, Issue 3, March 2010, Pages 476-483
نویسندگان
Ralf Frederik Claas, Michael ter Braak, Bianca Hegen, Verena Hardel, Carlo Angioni, Helmut Schmidt, Karl H. Jakobs, Paul P. Van Veldhoven, Dagmar Meyer zu Heringdorf,