Aleu Jordi, Martín-Satué Mireia, Navarro Piedad, Pérez de Lara Ivanna, Bahima Laia, Marsal Jordi, Solsona Carles
Laboratory of Molecular and Cellular Neurobiology, Department of Cell Biology, Medical School, Hospital of Bellvitge, University of Barcelona-Campus of Bellvitge, Feixa Llarga s/n, L' Hospitalet de Llobregat, E-08907 Spain.
J Physiol. 2003 Feb 15;547(Pt 1):209-19. doi: 10.1113/jphysiol.2002.029660. Epub 2002 Dec 20.
ATP mediates intercellular communication. Mechanical stress and changes in cell volume induce ATP release from various cell types, both secretory and non-secretory. In the present study, we stressed Xenopus oocytes with a hypertonic solution enriched in mannitol (300 mM). We measured simultaneously ATP release and ionic currents from a single oocyte. A decrease in cell volume, the activation of an inward current and ATP release were coincident. We found two components of ATP release: the first was associated with granule or vesicle exocytosis, because it was inhibited by tetanus neurotoxin, and the second was related to the inward current. A single exponential described the correlation between ATP release and the hypertonic-activated current. Gadolinium ions, which block mechanically activated ionic channels, inhibited the ATP release and the inward current but did not affect the decrease in volume. Oocytes expressing CFTR (cystic fibrosis transmembrane regulator) released ATP under hypertonic shock, but ATP release was significantly inhibited in the first component: that related to granule exocytosis. Since the ATP measured is the balance between ATP release and ATP degradation by ecto-enzymes, we measured the nucleoside triphosphate diphosphohydrolase (NTPDase) activity of the oocyte surface during osmotic stress, as the calcium-dependent hydrolysis of ATP, which was inhibited by more than 50 % in hypertonic conditions. The best-characterized membrane protein showing NTPDase activity is CD39. Oocytes injected with an antisense oligonucleotide complementary to CD39 mRNA released less ATP and showed a lower amplitude in the inward current than those oocytes injected with water.
三磷酸腺苷(ATP)介导细胞间通讯。机械应力和细胞体积变化可诱导各种细胞类型(包括分泌型和非分泌型细胞)释放ATP。在本研究中,我们用富含甘露醇(300 mM)的高渗溶液处理非洲爪蟾卵母细胞。我们同时测量了单个卵母细胞的ATP释放和离子电流。细胞体积减小、内向电流激活和ATP释放是同时发生的。我们发现ATP释放有两个成分:第一个成分与颗粒或囊泡胞吐作用有关,因为它受到破伤风神经毒素的抑制,第二个成分与内向电流有关。一个单指数描述了ATP释放与高渗激活电流之间的相关性。钆离子可阻断机械激活的离子通道,抑制ATP释放和内向电流,但不影响体积减小。表达囊性纤维化跨膜传导调节因子(CFTR)的卵母细胞在高渗休克下释放ATP,但在与颗粒胞吐作用相关的第一个成分中,ATP释放受到显著抑制。由于所测量的ATP是ATP释放与外切酶对ATP降解之间的平衡,我们在渗透应激期间测量了卵母细胞表面的核苷三磷酸二磷酸水解酶(NTPDase)活性,即ATP的钙依赖性水解,在高渗条件下其受到超过50%的抑制。表现出NTPDase活性的最具特征的膜蛋白是CD39。注射与CD39 mRNA互补的反义寡核苷酸的卵母细胞比注射水的卵母细胞释放的ATP更少,并且内向电流的幅度更低。