Calcium regulates the PI3K-Akt pathway in stretched osteoblasts

Theodora E. Danciu, Rosalyn M. Adam, Keiji Naruse, Michael R. Freeman, Peter V. Hauschka

Research output: Contribution to journalArticle

116 Citations (Scopus)

Abstract

Mechanical loading plays a vital role in maintaining bone architecture. The process by which osteoblasts convert mechanical signals into biochemical responses leading to bone remodeling is not fully understood. The earliest cellular response detected in mechanically stimulated osteoblasts is an increase in intracellular calcium concentration ([Ca2+]i). In this study, we used the clonal mouse osteoblast cell line MC3T3-E1 to show that uniaxial cyclic stretch induces: (1) an immediate increase in [Ca2+]i, and (2) the phosphorylation of critical osteoblast proteins that are implicated in cell proliferation, gene regulation, and cell survival. Our data suggest that cyclic stretch activates the phosphoinositide 3-kinase (PI3K) pathway including: PI3K, Akt, FKHR, and AFX. Moreover, cyclic stretch also causes the phosphorylation of stress-activated protein kinase/c-Jun N-terminal kinase. Attenuation in the level of phosphorylation of these proteins was observed by stretching cells in Ca2+-free medium, using intra- (BAPTA-AM) and extracellular (BAPTA) calcium chelators, or gadolinium, suggesting that influx of extracellular calcium plays a significant role in the early response of osteoblasts to mechanical stimuli.

Original languageEnglish
Pages (from-to)193-197
Number of pages5
JournalFEBS Letters
Volume536
Issue number1-3
DOIs
Publication statusPublished - Feb 11 2003
Externally publishedYes

Keywords

  • Akt
  • Calcium
  • Osteoblast
  • Stress-activated protein kinase/c-Jun N-terminal kinase
  • Stretch

ASJC Scopus subject areas

  • Biophysics
  • Structural Biology
  • Biochemistry
  • Molecular Biology
  • Genetics
  • Cell Biology

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  • Cite this

    Danciu, T. E., Adam, R. M., Naruse, K., Freeman, M. R., & Hauschka, P. V. (2003). Calcium regulates the PI3K-Akt pathway in stretched osteoblasts. FEBS Letters, 536(1-3), 193-197. https://doi.org/10.1016/S0014-5793(03)00055-3