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Alteration of intracellular free calcium and acylphosphatase levels in differentiating SH-SY5Y neuroblastoma cells.

Abstract
Levels of acylphosphatase isoenzymes and free intracellular calcium have been investigated in cultured SH-SY5Y human neuroblastoma cells under stimulation with all-trans retinoic acid and phorbol-12-myristate-13-acetate. Under these conditions morphological and functional characteristics demonstrated the differentiation of SH-SY5Y cells towards neuronal phenotype. Retinoic acid treatment caused a progressive and synchronous increase of the organ common-type acylphosphatase and of free intracellular calcium but not of the muscle-type acylphosphatase. Phorbol-12-myristate-13-acetate treatment gave rise to a peak of the muscle-type acylphosphatase levels during the early differentiation stage whereas organ common-type isoenzyme and free calcium levels show a pattern similar to that observed in retinoic acid-treated cells. These evidences indicate that the two acylphosphatase isoenzymes play different roles in SH-SY5Y differentiation and that during this process the expression of organ common-type acylphosphatase increases in a synchronous way with intracellular free calcium concentration.
AuthorsA Pieri, G Liguri, C Cecchi, D Degl'Innocenti, P Nassi, G Ramponi
JournalBiochemistry and molecular biology international (Biochem Mol Biol Int) Vol. 43 Issue 3 Pg. 633-41 (Oct 1997) ISSN: 1039-9712 [Print] England
PMID9352082 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Carcinogens
  • Neoplasm Proteins
  • Phorbol Esters
  • Tretinoin
  • Acid Anhydride Hydrolases
  • acylphosphatase
  • Calcium
Topics
  • Acid Anhydride Hydrolases (drug effects, metabolism)
  • Calcium (metabolism)
  • Carcinogens (pharmacology)
  • Cell Differentiation (drug effects)
  • Cell Division (drug effects)
  • Humans
  • Neoplasm Proteins (drug effects, metabolism)
  • Neuroblastoma (metabolism, pathology)
  • Phorbol Esters (pharmacology)
  • Time Factors
  • Tretinoin (pharmacology)
  • Tumor Cells, Cultured (drug effects)

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