Biolistic delivery of Ca2+ dyes into plant and algal cells

被引:28
作者
Bothwell, JHF
Brownlee, C
Hetherington, AM
Ng, CKY
Wheeler, GL
McAinsh, MR
机构
[1] Marine Biol Assoc United Kingdom Lab, Plymouth PL1 2PB, Devon, England
[2] Univ Lancaster, Lancaster Environm Ctr, Dept Biol Sci, Lancaster LA1 4YQ, England
[3] Univ Coll Dublin, Dept Bot, Dublin 4, Ireland
[4] Plymouth Marine Lab, Plymouth PL1 3DH, Devon, England
基金
英国生物技术与生命科学研究理事会;
关键词
cytosolic calcium; Commelina; Chlamydomonas; Fucus; biolistic; fluorescent dyes;
D O I
10.1111/j.1365-313X.2006.02687.x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
In eukaryotes, changes in cytosolic Ca2+ concentrations ([Ca2+](cyt)) are associated with a number of environmental and developmental stimuli. However, measuring [Ca2+](cyt) changes in single plant or algal cells is often problematic. Although a wide range of Ca2+-sensitive fluorescent dyes is available, they are often difficult to introduce into plant cells. Micro-injection is the most robust method for dye loading, but is time-consuming, technically demanding, and unsuitable in many cell types. To overcome these problems, we have adapted biolistic techniques to load Ca2+-sensitive dyes into guard cells of the flowering plant, Commelina communis, cells of the green alga Chlamydomonas reinhardtii, and zygotes of the brown alga, Fucus serratus. Using this approach, we have been able to monitor [Ca2+](cyt) changes in response to various stimuli, including a novel [Ca2+](cyt) response in C. reinhardtii. The method allows the use of free acid and dextran-conjugated dyes. Biolistic loading of differentiated plant cells is easier, quicker, and more widely applicable than micro-injection, and should broaden the study of plant signal transduction.
引用
收藏
页码:327 / 335
页数:9
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