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破骨细胞生成、骨骼衰老和骨疾病中的活性氧和氧化应激

Reactive oxygen species and oxidative stress in osteoclastogenesis, skeletal aging and bone diseases.

作者信息

Callaway Danielle A, Jiang Jean X

机构信息

Department of Biochemistry, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX, 78229-3900, USA.

出版信息

J Bone Miner Metab. 2015 Jul;33(4):359-70. doi: 10.1007/s00774-015-0656-4. Epub 2015 Mar 26.

Abstract

Osteoclasts are cells derived from bone marrow macrophages and are important in regulating bone resorption during bone homeostasis. Understanding what drives osteoclast differentiation and activity is important when studying diseases characterized by heightened bone resorption relative to formation, such as osteoporosis. In the last decade, studies have indicated that reactive oxygen species (ROS), including superoxide and hydrogen peroxide, are crucial components that regulate the differentiation process of osteoclasts. However, there are still many unanswered questions that remain. This review will examine the mechanisms by which ROS can be produced in osteoclasts as well as how it may affect osteoclast differentiation and activity through its actions on osteoclastogenesis signaling pathways. In addition, the contribution of ROS to the aging-associated disease of osteoporosis will be addressed and how targeting ROS may lead to the development of novel therapeutic treatment options.

摘要

破骨细胞是源自骨髓巨噬细胞的细胞,在骨稳态过程中调节骨吸收方面起着重要作用。在研究以骨吸收相对于骨形成增加为特征的疾病(如骨质疏松症)时,了解驱动破骨细胞分化和活性的因素非常重要。在过去十年中,研究表明活性氧(ROS),包括超氧化物和过氧化氢,是调节破骨细胞分化过程的关键成分。然而,仍有许多未解决的问题。本综述将探讨破骨细胞中ROS产生的机制,以及它如何通过对破骨细胞生成信号通路的作用影响破骨细胞的分化和活性。此外,还将讨论ROS对与衰老相关的骨质疏松症疾病的影响,以及靶向ROS如何可能导致新型治疗方案的开发。

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