Peer Reviewed

1

Document Type

Article

Publication Date

1-1-2015

Keywords

Animals, Bone Density Conservation Agents, Bone Remodeling, Bone and Bones, Diphosphonates, Imidazoles, Mice, Osteoblasts, Osteoclasts, Osteocytes, Osteogenesis, Osteoporosis

Funder/Sponsor

This work was funded by Science Foundation Ireland under the Research Frontiers Programme grant number RFPENM-991. The MLO-Y4 cells were generously provided by Dr. Linda Bonewald (School of Dentistry, University of Missouri, Kansas City, MO, USA).

Comments

This article is available with the kind permission of full reproduction from eCM journal (http://www.ecmjournal.org). Founded by scientists for the benefit of Science rather than profit.

http://www.ecmjournal.org/journal/papers/vol030/vol030a19.php

Abstract

Osteoporosis is one of the most prevalent bone diseases worldwide and is characterised by high levels of bone turnover, a marked loss in bone mass and accumulation of microdamage, which leads to an increased fracture incidence that places a huge burden on global health care systems. Bisphosphonates have been used to treat osteoporosis and have shown great success in conserving bone mass and reducing fracture incidence. In spite of the existing knowledge of the in vivo responses of bone to bisphosphonates, the cellular responses to these drugs have yet to be fully elucidated. In vitro model systems that allow the decoupling of complex highly integrated events, such as bone remodelling, provide a tool whereby these biological processes may be studied in a more simplified context. This study firstly utilised an in vitro model system of bone remodelling and comprising all three major cell types of the bone (osteocytes, osteoclasts and osteoblasts), which was representative of the bone's capacity to sense microdamage and subsequently initiate a basic multicellular unit response. Secondly, this system was used to study the effect of two commonly utilised aminobisphosphonate treatments for osteoporosis, alendronate and zoledronate. We demonstrated that microinjury to osteocyte networks being treated with bisphosphonates modulates receptor activator of nuclear factor kappa-B ligand and osteoprotegerin activity, and subsequently osteoclastogenesis. Furthermore, bisphosphonates increased the osteogenic potential following microinjury. Thus, we have shown for the first time that bisphosphonates act at all three stages of bone remodelling, from microinjury to osteoclastogenesis and ultimately osteogenesis.

Disciplines

Anatomy

Citation

Mulcahy LE, Curtin CM, McCoy RJ, O'Brien FJ, Taylor D, Lee TC, Duffy GP. The effect of bisphosphonate treatment on the biochemical and cellular events during bone remodelling in response to microinjury stimulation. European Cells & Materials. 2015;30:271-81.

PubMed ID

26614482

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