Halperin Stephen J, Lynch Jonathan P
Department of Horticulture, The Pennsylvania State University, 102 Tyson Bldg., University Park, PA 16802, USA.
J Exp Bot. 2003 Sep;54(390):2035-43. doi: 10.1093/jxb/erg219.
Toxicity from sodium accumulation is an important aspect of salinity stress that has been well studied at the organ and tissue level. However, the effects of salinity on sodium accumulation in the cytosol, where much of the sodium toxicity is thought to occur, are poorly understood due to the difficulty of direct non-invasive measurements of ion activities in living cells. The Na+-sensing fluorescent probe sodium-binding benzofuran isophthalate (SBFI) and the K+-sensing fluorescent probe potassium-binding benzofuran isophthalate (PBFI) were used to quantify Na+ and K+ activity in living root hairs under salinity stress. The effects of exposure of Arabidopsis thaliana roots to 0, 30, 60 or 90 mM NaCl were observed during the 20 min immediately following salinization and also after 2 d of salinization, in plants supplied with 0.5, 2.0 or 5.0 mM Ca. SBFI and PBFI fluorescence was confined primarily to the cytoplasm, with very little signal from the vacuole. Sodium affected the quantification of K+ by PBFI, thus limiting the usefulness of this dye. Root hairs exposed to NaCl accumulated from 30-60 mM Na+ within the first 5 min of salinization in 0.5 and 2.0 mM Ca2+, and up to 15 mM Na+ in the 5.0 mM Ca2+ treatment. Two days of salinization did not increase cytosolic Na+ concentrations beyond the values observed after 20 min of salinization. Cytosolic activities roughly corresponded with elemental analysis of combined dry matter fractions from whole plants. We conclude that SBFI and, to a lesser extent, PBFI are useful tools for quantifying the dynamics of ion activities in the cytosols of living plant cells.
钠积累导致的毒性是盐胁迫的一个重要方面,这在器官和组织水平上已经得到了充分研究。然而,由于难以对活细胞中的离子活性进行直接非侵入性测量,人们对盐度对细胞质中钠积累的影响了解甚少,而钠毒性大多被认为发生在细胞质中。钠敏感荧光探针钠结合苯并呋喃异邻苯二甲酸酯(SBFI)和钾敏感荧光探针钾结合苯并呋喃异邻苯二甲酸酯(PBFI)被用于量化盐胁迫下活根毛中的Na⁺和K⁺活性。在盐化后的20分钟内以及盐化2天后,观察了拟南芥根暴露于0、30、60或90 mM NaCl的影响,这些植物分别供应0.5、2.0或5.0 mM Ca。SBFI和PBFI荧光主要局限于细胞质,液泡中的信号非常少。钠影响了PBFI对K⁺的量化,因此限制了这种染料的用途。在0.5和2.0 mM Ca²⁺处理中,暴露于NaCl的根毛在盐化的前5分钟内积累了30 - 60 mM的Na⁺,在5.0 mM Ca²⁺处理中积累了高达15 mM的Na⁺。盐化两天后,细胞质中的Na⁺浓度并未超过盐化20分钟后观察到的值。细胞质活性大致与全株混合干物质部分的元素分析结果相符。我们得出结论,SBFI以及在较小程度上的PBFI是量化活植物细胞细胞质中离子活性动态的有用工具。