1998
DOI: 10.1016/s0898-6568(97)00197-6
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Phospholipase D

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Cited by 100 publications
(17 citation statements)
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“…Hence, it is unlikely that increases in [Ca 2ϩ ] cyt are the direct cause of the elevation in PLD activity, although such increases could function upstream in the PLD activation pathway. A further possibility is that PLD is activated by a G protein, as seen in many mammalian PLD-based signal transduction pathways (30). G protein activation of PLD also has been reported in Chlamydomonas (24,43), and there are extensive data implicating G proteins as intermediates in signal transduction in guard cells (40,44).…”
Section: Discussionmentioning
confidence: 92%
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“…Hence, it is unlikely that increases in [Ca 2ϩ ] cyt are the direct cause of the elevation in PLD activity, although such increases could function upstream in the PLD activation pathway. A further possibility is that PLD is activated by a G protein, as seen in many mammalian PLD-based signal transduction pathways (30). G protein activation of PLD also has been reported in Chlamydomonas (24,43), and there are extensive data implicating G proteins as intermediates in signal transduction in guard cells (40,44).…”
Section: Discussionmentioning
confidence: 92%
“…Phospholipase D (PLD) is involved in signaling in animals, and recent studies suggest a similar role in algae and plants (24)(25)(26)(27)(28)(29)(30)(31). PLD hydrolyzes phospholipids, producing phosphatidic acid (PtdOH) and the head group.…”
mentioning
confidence: 99%
“…The role of PA in VEGF-A signaling still remains to be investigated. In vitro, PA is a regulator of several signaling proteins, some of which are involved in VEGF-A signaling (English, 1996;Gomez-Cambronero and Keire, 1998;Topham and Prescott, 1999). For instance, VEGF-A activates PKCz, which is positively regulated by PA and Src tyrosine phosphorylation (Limatola et al, 1994;Seibenhener et al, 1999).…”
Section: Discussionmentioning
confidence: 99%
“…Also, the cells were preincubated with U73122, PAO, RO320432, GO6976, SB203580, or SB202190 for 30 min after being labeled with [ 3 H]palmitic acid and serum-starved for 20 h. After treatment with Der f 2 for 30 min, the cells were quickly washed with ice-cold phosphate-buffered saline and suspended in ice-cold methanol. Lipids were extracted according to the method of Bligh and Dyer (36), and PBt was separated by TLC using a acetate/isooctane/acetic acid/water (110:50:20: 100,v/v) solvent system. The regions corresponding to the authentic PBt bands were identified with 0.002% (w/v) primulin in 80% (v/v) acetone, scraped, and counted using a liquid scintillation counter.…”
Section: Methodsmentioning
confidence: 99%