2011
DOI: 10.1016/j.cellsig.2011.06.009
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Osmotic stabilizer-coupled suppression of NDR defects is dependent on the calcium–calcineurin signaling cascade in Aspergillus nidulans

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Cited by 16 publications
(23 citation statements)
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“…In filamentous fungi, hyphal branching is one of the essential phenotypes of polarized growth regulated by Ca 2+ (Silverman-Gavrila and Lew, 2003). In Aspergillus nidulans, the osmotic stabilizer-coupled suppression of the defects in the NDR (nuclear Dbf2-related) protein kinase signaling pathway is dependent on calcium-calcineurin signaling and might therefore regulate polarized cell growth (Gao et al, 2011). Similar phenomena were reported in Nox-silenced strains of G. lucidum in which lower Ca 2+ levels caused more hyphal branching (Mu et al, 2014).…”
Section: The Effects Of Gpx-regulated Ros On Hyphal Branching Might Osupporting
confidence: 52%
See 1 more Smart Citation
“…In filamentous fungi, hyphal branching is one of the essential phenotypes of polarized growth regulated by Ca 2+ (Silverman-Gavrila and Lew, 2003). In Aspergillus nidulans, the osmotic stabilizer-coupled suppression of the defects in the NDR (nuclear Dbf2-related) protein kinase signaling pathway is dependent on calcium-calcineurin signaling and might therefore regulate polarized cell growth (Gao et al, 2011). Similar phenomena were reported in Nox-silenced strains of G. lucidum in which lower Ca 2+ levels caused more hyphal branching (Mu et al, 2014).…”
Section: The Effects Of Gpx-regulated Ros On Hyphal Branching Might Osupporting
confidence: 52%
“…After Fluo-3 AM enters a cell, this dye is readily hydrolyzed into a Ca 2+ -binding form, Fluo-3, by an endogenous esterase (Gao et al, 2011). Subsequently, the Fluo-3-labeled cells were examined using a Zeiss Axio Imager.A1 Fluorescence Microscope; the cells were excited at 488 nm with an Ar laser, and fluorescence was detected using a 505-530 nm band pass filter.…”
Section: Detection and Labeling Of Free Cytosolic Ca 2+mentioning
confidence: 99%
“…Aspergillus nidulans strain FGSC A26 (biA1, veA1) was maintained according Vanzela and Said [12] and grown at 30˚C for seven days before inoculating them on the culture medium (MM) containing nitrate salts and trace elements prepared according to Käfer [13] supplemented with 0.5% glucose and 0.02 µg/mL biotin; 1.8% agar was added and the pH was adjusted to 6.0.…”
Section: Strains and Growth Conditionsmentioning
confidence: 99%
“…H9C2 cells were cultured and pretreated with 14,15-EET 1 hour before treatment with ISO (10 mM) or AngII (100 nM). Twenty-four hours later, the intracellular Ca 21 concentration was measured using a Fluo-3 AM kit from Invitrogen according to the supplier's instructions, as previously described (Gao et al, 2011). Relative intracellular Ca 21 was expressed as a percentage of the control.…”
mentioning
confidence: 99%