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将乙酰氧基甲基酯荧光染料载入拟南芥和鸭跖草保卫细胞的细胞质中。

Loading acetoxymethyl ester fluorescent dyes into the cytoplasm of Arabidopsis and Commelina guard cells.

作者信息

Kuchitsu Kazuyuki, Ward John M, Allen Gethyn J, Schelle Ilona, Schroeder Julian I

机构信息

University of California, San Diego, Division of Biology, Cell and Developmental Biology Section and Center for Molecular Genetics, La Jolla, CA 92093-0116, USA; 1Present address: Department of Applied Biological Science, Tokyo University of Science, Noda, Chiba, 278-8510 Japan; 2Present address: Department of Plant Biology, University of Minnesota, St. Paul, MN 55108-1095, USA.

出版信息

New Phytol. 2002 Mar;153(3):527-533. doi: 10.1046/j.0028-646X.2001.00346.x. Epub 2002 Mar 5.

Abstract

•  Cytosolic calcium and pH changes are integral components of guard cell signal transduction. Acetoxymethyl (AM) ester-linked Ca sensitive dyes are usually degraded before loading by extracellular esterases or partitioned into plant vacuoles using standard techniques, thereby preventing cytoplasmic Ca imaging. •  Here a method is described for improved loading of the calcium sensitive fluorescent dyes Calcium Green-1 and Fura-2 AM ester into the cytoplasm of Commelina and Arabidopsis guard cells in epidermal strips, allowing fluorescence from several guard cells in an epidermal strip to be imaged and measured simultaneously. •  Calcium Green-1 based imaging, external Ca buffering and Mn quenching in Commelina guard cells suggest that abscisic acid stimulates plasma membrane Ca influx. The Ca sensitive dye Fura-2 was loaded into the cytoplasm of Arabidopsis guard cells, allowing ratiometric analyses of these cells. Data indicated that intact Ca homeostasis mechanisms were present in Fura-2 AM loaded cells. •  Loading of acetoxymethyl ester dyes provides a viable alternative method to cameleon imaging, which will be useful in loading Arabidposis mutants that are difficult to transform. This method may also be applicable to loading other ester linked dyes into the cytoplasm of plant cells.

摘要

• 胞质钙和pH变化是保卫细胞信号转导的组成部分。乙酰氧基甲基(AM)酯连接的钙敏感染料通常在加载前被细胞外酯酶降解,或使用标准技术分配到植物液泡中,从而阻止细胞质钙成像。

• 本文描述了一种改进的方法,将钙敏荧光染料钙绿-1和Fura-2 AM酯加载到表皮条中鸭跖草和拟南芥保卫细胞的细胞质中,从而可以同时对表皮条中多个保卫细胞的荧光进行成像和测量。

• 基于钙绿-1的成像、外部钙缓冲和鸭跖草保卫细胞中的锰猝灭表明,脱落酸刺激质膜钙内流。钙敏染料Fura-2被加载到拟南芥保卫细胞的细胞质中,从而可以对这些细胞进行比率分析。数据表明,加载Fura-2 AM的细胞中存在完整的钙稳态机制。

• 乙酰氧基甲酯染料的加载为cameleon成像提供了一种可行的替代方法,这将有助于加载难以转化的拟南芥突变体。该方法也可能适用于将其他酯连接的染料加载到植物细胞的细胞质中。

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