Format

Send to

Choose Destination
Curr Osteoporos Rep. 2015 Apr;13(2):67-72. doi: 10.1007/s11914-015-0255-2.

Cx43 and mechanotransduction in bone.

Author information

1
Department of Anatomy and Cell Biology, Indiana University School of Medicine, and Roudebush Veterans Administration Medical Center, 635 Barnhill Drive, MS-5035, Indianapolis, IN, 46202, USA, lplotkin@iupui.edu.

Abstract

Bone adaptation to changes in mechanical stimuli occurs by adjusting bone formation and resorption by osteoblasts and osteoclasts, to maintain optimal bone mass. Osteocytes coordinate the actions of these cells on the bone surface by sensing mechanical forces and producing cytokines that increase or prevent osteoblast and osteoclast differentiation and function. Channels formed by connexins (Cxs) and, in particular, connexin 43 (Cx43) in osteoblasts and osteocytes are central part of this mechanism to control bone mass. Cx43 hemichannels are opened by fluid flow and mediate the anti-apoptotic effect of mechanical stimulation in vitro, suggesting that Cx43 participates in mechanotransduction. However, mice lacking Cx43 in osteoblasts and/or osteocytes show an increased anabolic response to loading and decreased catabolic response to unloading. This evidence suggests that Cx43 channels expressed in osteoblastic cells are not required for the response to mechanical stimulation, but mediate the consequence of lack thereof. The molecular basis of these unexpected responses to mechanical stimulation is currently under investigation.

PMID:
25616771
PMCID:
PMC4355098
DOI:
10.1007/s11914-015-0255-2
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Springer Icon for PubMed Central
Loading ...
Support Center