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Quantitative immunodetection of key elements of polyphosphoinositide signal transduction in osteoblasts from arthritic patients shows a direct correlation with cell proliferation.

Abstract
Phosphoinositides play an essential role in diverse cellular functions such as cell proliferation, cytoskeletal regulation, intracellular vesicle trafficking, motility, cell metabolism and death. Alteration of these pathways is common to many diseases. In this study, we show that osteoblasts from patients affected by osteoarthritis (OA) and by rheumatoid arthritis (RA) present a decreased cell proliferation and a reduced expression of the key elements of polyphosphoinositide signal transduction such as phosphatidylinositol-3-kinase (PI 3K), phospholipase C gamma1 (PLCgamma1), and protein kinase C zeta (PKCzeta) compared to the post-traumatic (PT) patients. Our results suggest that a correlation may exist between the reduced osteoblast proliferation observed in OA and RA patients and the lowered expression of PI 3K, PLCgamma1, and PKCzeta enzymes. The reduced proliferation rate of osteoblasts in response to these signal transduction effectors could counteract the evolution of arthritic disease.
AuthorsNicoletta Zini, Gina Lisignoli, Liliana Solimando, Alberto Bavelloni, Aurelio Valmori, Sandra Cristino, Alberto Maria Martelli, Andrea Facchini, Nadir Mario Maraldi
JournalHistochemistry and cell biology (Histochem Cell Biol) Vol. 124 Issue 2 Pg. 131-7 (Aug 2005) ISSN: 0948-6143 [Print] Germany
PMID16052323 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • Phosphatidylinositol Phosphates
  • Phosphatidylinositol 3-Kinases
  • protein kinase C zeta
  • Protein Kinase C
  • Type C Phospholipases
  • Phospholipase C gamma
Topics
  • Aged
  • Arthritis, Rheumatoid (enzymology, pathology)
  • Biomarkers (metabolism)
  • Cell Proliferation
  • Cells, Cultured
  • Female
  • Femur Head (cytology)
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Immunoenzyme Techniques
  • Male
  • Middle Aged
  • Osteoarthritis (enzymology, pathology)
  • Osteoblasts (metabolism, pathology)
  • Phosphatidylinositol 3-Kinases (metabolism)
  • Phosphatidylinositol Phosphates (metabolism)
  • Phospholipase C gamma
  • Protein Kinase C (metabolism)
  • Signal Transduction
  • Type C Phospholipases (metabolism)
  • Wounds and Injuries (metabolism, pathology)

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