Absence of Cx43 selectively from osteocytes enhances responsiveness to mechanical force in mice. Issue 7 (11th March 2013)

• Record Type: Journal Article
• Authors: Bivi, Nicoletta; Pacheco‐Costa, Rafael; Brun, Lucas R.; Murphy, Thomas R.; Farlow, Nathan R.; Robling, Alexander G.; Bellido, Teresita; Plotkin, Lilian I.
• Is Part Of: Journal of orthopaedic research. Volume 31:Issue 7(2013:Jul.)
• Page Start: 1075
• Page End: 1081
• Publication Date: 2013-03-11
• Subjects: Orthopedics -- Periodicals; Musculoskeletal system -- Periodicals; 616.7
• DOI: 10.1002/jor.22341
• Languages: English
• ISSNs: 0736-0266

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="jor22341-sec-0001" sec-type="section"> <p>The osteocyte network is crucial for the response of bone to mechanical force. Within this network, connexin43 (Cx43) is thought to mediate the communication of osteocytes and osteoblasts among themselves and the exchange of small molecules with the extracellular milieu. Despite recent advances in understanding Cx43 role for the response of bone cells to mechanical stimulation, the contribution of Cx43 specifically in osteocytes to mechanotransduction in vivo is not well‐known. We examined the anabolic response to ulnar axial loading of mice lacking Cx43 in osteocytes (Cx43<sup>ΔOt</sup>). Loading induced a greater increase in periosteal bone formation rate in Cx43<sup>ΔOt</sup> mice compared to control littermates, resulting from higher mineralizing surface and enhanced mineral apposition rate. Expression of β‐catenin protein, a molecule implicated in mechanotransduction, was higher in bones from Cx43<sup>ΔOt</sup> mice, compared to littermate controls. In addition, MLO‐Y4 osteocytic cells knocked‐down for Cx43 exhibited higher β‐catenin protein expression and enhanced response to mechanical stimulation. These findings suggest that osteocytes lacking Cx43 are "primed" to respond to mechanical stimulation and that absence of Cx43 in osteocytes unleashes bone formation, by a mechanism that might involve accumulation of β‐catenin. © 2013 Orthopaedic Research Society Published by Wiley Periodicals, Inc. J Orthop Res 31:1075–1081, 2013</p> </sec> </abstract>