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First published online January 26, 2007; 10.1104/pp.106.091405 Plant Physiology 143:1140-1151 (2007) © 2007 American Society of Plant Biologists OPEN ACCESS ARTICLE
Osmo-Sensitive and Stretch-Activated Calcium-Permeable Channels in Vicia faba Guard Cells Are Regulated by Actin Dynamics1,[OA]State Key Laboratory of Plant Physiology and Biochemistry, College of Biological Sciences, China Agricultural University, Beijing 100094, China
In responses to a number of environmental stimuli, changes of cytoplasmic [Ca2+]cyt in stomatal guard cells play important roles in regulation of stomatal movements. In this study, the osmo-sensitive and stretch-activated (SA) Ca2+ channels in the plasma membrane of Vicia faba guard cells are identified, and their regulation by osmotic changes and actin dynamics are characterized. The identified Ca2+ channels were activated under hypotonic conditions at both whole-cell and single-channel levels. The channels were also activated by a stretch force directly applied to the membrane patches. The channel-mediated inward currents observed under hypotonic conditions or in the presence of a stretch force were blocked by the Ca2+ channel inhibitor Gd3+. Disruption of actin filaments activated SA Ca2+ channels, whereas stabilization of actin filaments blocked the channel activation induced by stretch or hypotonic treatment, indicating that actin dynamics may mediate the stretch activation of these channels. In addition, [Ca2+]cyt imaging demonstrated that both the hypotonic treatment and disruption of actin filaments induced significant Ca2+ elevation in guard cell protoplasts, which is consistent with our electrophysiological results. It is concluded that stomatal guard cells may utilize SA Ca2+ channels as osmo sensors, by which swelling of guard cells causes elevation of [Ca2+]cyt and consequently inhibits overswelling of guard cells. This SA Ca2+ channel-mediated negative feedback mechanism may coordinate with previously hypothesized positive feedback mechanisms and regulate stomatal movement in response to environmental changes.
1 This work was supported by the National Science Foundation of China (a competitive fund for Creative Research Groups; grant no. 30421002) and by the Chinese National Key Basic Research Project (grant no. 2006CB100100 to W.H.W.). 2 Present address: Peking-Yale Joint Center for Plant Molecular Genetics and Agro-Biotechnology, State Key Laboratory of Protein Engineering and Plant Genetic Engineering, College of Life Sciences, Peking University, Beijing 100871, China. The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantphysiol.org) is: Wei-Hua Wu (wuwh{at}public3.bta.net.cn). [OA] Open Access articles can be viewed online without a subscription. www.plantphysiol.org/cgi/doi/10.1104/pp.106.091405 * Corresponding author; e-mail wuwh{at}public3.bta.net.cn; fax 861062734640. Received October 21, 2006; accepted January 12, 2007; published January 26, 2007. This article has been cited by other articles:
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