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Aluminum ions inhibit phospholipase D in a microtubule-dependent manner

Tipo de material: TextoTextoSeries ; Cell Biology International, 32, p.554-556, 2008Trabajos contenidos:
  • Pejchar, P
  • Pleskot, R
  • Schwarzerova, K
  • Martinec, J
  • Valentova, O
  • Novotna, Z
Tema(s): Recursos en línea: Resumen: Aluminum is a highly cytotoxic metal to plants, but the molecular base and the primary target of Al toxicity are still unknown. The most important physiological consequence of Al toxicity is a cessation of root growth and changes in root morphology suggesting a role of the root cytoskeleton as a target structure. The important role of phospholipid degrading enzyme phospholipase D in regulation of cytoskeleton remodelling in both animal and plant organisms is now evident. Both the phospholipid pathway and the cytoskeleton are influenced by Al3þ, but their relationship with Al stress remains to be explored. Therefore, we tested the possibility that Al stress could e sensed by plants through microtubules in close interaction with phospholipases. We have shown that Al3þ reduced the formation of phosphatidic acid in vivo, inhibited activity of phosphatidylinositol-4,5-bisphosphate-dependent phospholipase D in vitro and that the phosphatidic acid production is modified by microtubule dynamics.
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Aluminum is a highly cytotoxic metal to plants, but the molecular base and the primary target of Al toxicity are still unknown. The most important physiological consequence of Al toxicity is a cessation of root growth and changes in root morphology suggesting a role of the root cytoskeleton as a target structure. The important role of phospholipid degrading enzyme phospholipase D in regulation of cytoskeleton remodelling in both animal and plant organisms is now evident. Both the phospholipid pathway and the cytoskeleton are influenced by Al3þ, but their relationship with Al stress remains to be explored. Therefore, we tested the possibility that Al stress could e sensed by plants through microtubules in close interaction with phospholipases. We have shown that Al3þ reduced the formation of phosphatidic acid in vivo, inhibited activity of phosphatidylinositol-4,5-bisphosphate-dependent phospholipase D in vitro and that the phosphatidic acid production is modified by microtubule dynamics.

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