Weitzmann M Neale, Pacifici Roberto
Division of Endocrinology, Metabolism, and Lipids and Molecular Pathogenesis Program, Emory University, Atlanta, Georgia 30322, USA.
J Clin Invest. 2006 May;116(5):1186-94. doi: 10.1172/JCI28550.
Estrogen plays a fundamental role in skeletal growth and bone homeostasis in both men and women. Although remarkable progress has been made in our understanding of how estrogen deficiency causes bone loss, the mechanisms involved have proven to be complex and multifaceted. Although estrogen is established to have direct effects on bone cells, recent animal studies have identified additional unexpected regulatory effects of estrogen centered at the level of the adaptive immune response. Furthermore, a potential role for reactive oxygen species has now been identified in both humans and animals. One major challenge is the integration of a multitude of redundant pathways and cytokines, each apparently capable of playing a relevant role, into a comprehensive model of postmenopausal osteoporosis. This Review presents our current understanding of the process of estrogen deficiency-mediated bone destruction and explores some recent findings and hypotheses to explain estrogen action in bone. Due to the inherent difficulties associated with human investigation, many of the lessons learned have been in animal models. Consequently, many of these principles await further validation in humans.
雌激素在男性和女性的骨骼生长及骨稳态中发挥着重要作用。尽管我们在理解雌激素缺乏如何导致骨质流失方面取得了显著进展,但相关机制已被证明是复杂且多方面的。虽然雌激素对骨细胞的直接作用已得到证实,但最近的动物研究发现了雌激素在适应性免疫反应水平上的其他意外调节作用。此外,现在已经在人类和动物中确定了活性氧的潜在作用。一个主要挑战是将众多冗余途径和细胞因子整合到一个全面的绝经后骨质疏松症模型中,每个途径和细胞因子显然都能发挥相关作用。本综述介绍了我们目前对雌激素缺乏介导的骨破坏过程的理解,并探讨了一些最新发现和假设,以解释雌激素在骨骼中的作用。由于人体研究存在固有的困难,许多经验教训来自动物模型。因此,许多这些原理有待在人体中进一步验证。