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Research Database PMU-SQQUID

Mechanical regulation of HB-GAM expression in bone cells.
Liedert, A; Augat, P; Ignatius, A; Hausser, HJ; Claes, L;
Biochem Biophys Res Commun. 2004; 319(3):951-958
Full papers/articles (Journal)

PMU-Authors

Augat Peter

Abstract

Bone adaption upon mechanical stimulation is accompanied by changes in gene expression. In this context we investigated the influence of mechanical loading on heparin binding growth associated molecule (HB-GAM) expression, an extracellular matrix molecule which in cell culture has been shown to stimulate the differentiation of osteoblasts. We obtained information on the participating signal transduction pathways using a mitogenic loading regimen. Specific inhibitors of various signal transduction pathways were added to loaded cells and to unloaded controls. By semi-quantitative PCR studies we demonstrated a rapid decrease of HB-GAM expression in primary osteoblasts and SaOs-2 cells by 20-30% upon mechanical loading within 30min. We showed that the RGD-integrin interaction is involved in the regulation of HB-GAM expression. Furthermore, integrity of the cytoskeleton, stretch-activated, and voltage-sensitive Ca2+ channels as well as gap junctional communication are necessary for the downregulation of HB-GAM expression by mechanical loading. (C) 2004 Elsevier Inc. All rights reserved.


Useful keywords (using NLM MeSH Indexing)

Aged

Carrier Proteins/genetics

Carrier Proteins/metabolism*

Cells, Cultured

Cytokines/genetics

Cytokines/metabolism*

Cytoskeleton/metabolism

Female

Gene Expression Regulation*

Glycyrrhetinic Acid/chemistry

Glycyrrhetinic Acid/pharmacology

Humans

Integrins/genetics

Integrins/metabolism

Male

Middle Aged

Mitogens/metabolism*

Oligopeptides/genetics

Oligopeptides/metabolism

Osteoblasts/cytology

Osteoblasts/drug effects

Osteoblasts/physiology*

Signal Transduction/physiology

Stress, Mechanical


Find related publications in this database (Keywords)

heparin-binding growth-associated molecule
osteoblasts
mechanical loading
mechanotransduction
signal transduction
cytoskeleton
integrins
calcium channels
gap junctional communication