Bone Remodeling Under Pathological Conditions.

Frontiers of oral physiology Pub Date : 2016-01-01 Epub Date: 2015-11-24 DOI:10.1159/000351896
Wenmei Xiao, Shuai Li, Sandra Pacios, Yu Wang, Dana T Graves
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引用次数: 52

Abstract

Bone is masterfully programmed to repair itself through the coupling of bone formation following bone resorption, a process referred to as coupling. In inflammatory or other conditions, the balance between bone resorption and bone formation shifts so that a net bone loss results. This review focuses on four pathologic conditions in which remodeling leads to net loss of bone, postmenopausal osteoporosis, arthritis, periodontal disease, and disuse bone loss, which is similar to bone loss associated with microgravity. In most of these there is an acceleration of the resorptive process due to increased formation of bone metabolic units. This initially leads to a net bone loss since the time period of resorption is much faster than the time needed for bone formation that follows. In addition, each of these processes is characterized by an uncoupling that leads to net bone loss. Mechanisms responsible for increased rates of bone resorption, i.e. the formation of more bone metabolic units, involve enhanced expression of inflammatory cytokines and increased expression of RANKL. Moreover, the reasons for uncoupling are discussed which range from a decrease in expression of growth factors and bone morphogenetic proteins to increased expression of factors that inhibit Wnt signaling.

病理条件下的骨重塑
骨骼通过骨吸收后骨形成的耦合过程进行自我修复,这一过程被称为耦合。在炎症或其他情况下,骨吸收和骨形成之间的平衡会发生变化,从而导致骨质净流失。本综述将重点讨论重塑导致骨质净流失的四种病理情况,即绝经后骨质疏松症、关节炎、牙周病和废用性骨质流失(类似于微重力引起的骨质流失)。在大多数情况下,由于骨代谢单位的形成增加,吸收过程会加快。这最初会导致骨质净流失,因为骨吸收的时间远远快于随后骨形成所需的时间。此外,这些过程中的每一个过程都具有导致净骨丢失的脱钩特征。导致骨吸收率增加(即形成更多的骨代谢单位)的机制包括炎症细胞因子的表达增强和 RANKL 的表达增加。此外,还讨论了导致解耦的原因,包括生长因子和骨形态发生蛋白表达的减少,以及抑制 Wnt 信号转导的因子表达的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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