The stomata of maize (Zea mays) contain a pair of guard cells and a pair of subsidiary cells. To determine whether HO, Ca, and K in subsidiary cells were involved in stomatal movement, we treated four-week-old maize (Zhengdan 958) leaves with HO, diphenylene iodonium (DPI), CaCl, and LaCl. Changes in content and distribution of HO, Ca, and K during stomatal movement were observed. When exogenous HO was applied, Ca increased and K decreased in guard cells, while both ions increased in subsidiary cells, leading to stomatal closure. After DPI treatment, Ca decreased and K increased in guard cells, but both Ca and K decreased in subsidiary cells, resulting in open stomata. Exogenous CaCl increased HO and reduced K in guard cells, while significantly increasing them in subsidiary cells and causing stomatal closure. After LaCl treatment, HO decreased and K increased in guard cells, whereas both decreased in subsidiary cells and stomata became open. Results indicate that HO and Ca correlate positively with each other and with K in subsidiary cells during stomatal movement. Both HO and Ca in subsidiary cells promote an inflow of K, indirectly regulating stomatal closure.
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http://dx.doi.org/10.1016/j.plaphy.2020.04.045 | DOI Listing |
New Phytol
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Facultad de Ciencias Ambientales y Bioquímica, Universidad de Castilla-La Mancha, E-45071, Toledo, Spain.
SLAS Discov
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iBET, Instituto de Biologia Experimental e Tecnológica, Apartado 12 2781-901 Oeiras, Portugal; ITQB NOVA, Instituto de Tecnologia Química e Biológica António Xavier, Av. Republica, 2780-157, Oeiras, Portugal. Electronic address:
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Laboratory of Translational Oncology and Experimental Cancer Therapeutics, The Warren Alpert Medical School, Brown University Providence, RI 02903, USA.
Androgen receptor (AR) signaling is a target in prostate cancer therapy and can be treated with non-steroidal anti-androgens (NSAA) including enzalutamide, and apalutamide for patients with advanced disease. Metastatic castration-resistant prostate cancer (mCPRC) develop resistance becomes refractory to therapy limiting patient overall survival. Darolutamide is a novel next-generation androgen receptor-signaling inhibitor that is FDA approved for non-metastatic castration resistant prostate cancer (nmCRPC).
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Department of Pediatrics, Johns Hopkins University, Baltimore, MD.
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