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Calcium regulates the PI3K‐Akt pathway in stretched osteoblasts
Author(s) -
Danciu Theodora E,
Adam Rosalyn M,
Naruse Keiji,
Freeman Michael R,
Hauschka Peter V
Publication year - 2003
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/s0014-5793(03)00055-3
Subject(s) - microbiology and biotechnology , pi3k/akt/mtor pathway , extracellular , osteoblast , phosphorylation , bapta , protein kinase b , calcium , chemistry , kinase , calcium in biology , intracellular , signal transduction , biochemistry , biology , in vitro , organic chemistry
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 ([Ca 2+ ] 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 [Ca 2+ ] 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 Ca 2+ ‐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.