2009
DOI: 10.1007/s00784-009-0268-2
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The molecular mechanism behind bone remodelling: a review

Abstract: Bone is a connective tissue and guarantees protection and support of organ function. Contrary to the common view, bone is a dynamic tissue that constantly undergoes turnover in order to maintain stability and integrity. In this process called bone turnover or bone remodelling, two effector cell types are involved. Osteoclasts, specialised for bone resorption, and osteoblasts, responsible for bone formation, are key players in bone turnover. In the past decade, a lot of information about signal pathways, osteob… Show more

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Cited by 146 publications
(120 citation statements)
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“…The second, and most problematic issue, is that bones experiencing mechanical loading are subject to remodeling throughout the life of the individual [56]. Consequently, individual asymmetry of a trait can change over time [57].…”
Section: Skeletal Asymmetrymentioning
confidence: 99%
“…The second, and most problematic issue, is that bones experiencing mechanical loading are subject to remodeling throughout the life of the individual [56]. Consequently, individual asymmetry of a trait can change over time [57].…”
Section: Skeletal Asymmetrymentioning
confidence: 99%
“…Osteoclastogenesis precedes with the expression of RANKL by bone lining cells, which in turn binds to the RANK that exists as a surface receptor on the membrane of preosteoclasts. The receptor-ligand binding promotes an intricate and distinct signaling cascade for osteoclast activation and commitment [21,22]. The expression of RANKL is up-regulated in the presence of interleukin-1 (IL-1), tumor necrosis factor α (TNF-α) and vitamin D, whereas transforming growth factor β (TGFβ) and estrogens have an opposite effect.…”
Section: Bone Remodelingmentioning
confidence: 99%
“…This process is important to maintain the stability and integrity of the skeleton (Proff and Römer, 2009). It occurs in small packs of cells called basic multicellular unit (BMUs) which comprises osteoclasts and osteoblasts (Hill and Orth, 1998).…”
Section: Bone Turnovermentioning
confidence: 99%
“…osteoclasts (Boyce and Xing, 2008). The osteoclast progenitors differentiate into osteoclasts and start breaking down bone and liberating bone morphogenetic proteins (BMPs) and insulin-like growth factor II, which will then stimulate osteoblast cells (Proff and Römer, 2009). The transition from the resorption phase to formation is comprised by the reversal phase where there is a discontinuation of osteoclast action by apoptosis followed by the differentiation of osteoblast precursors into active osteoblasts (Hill and Orth, 1998).…”
Section: Bone Turnovermentioning
confidence: 99%
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