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c-Maf 和你不会看到脂肪。

c-Maf and you won't see fat.

机构信息

Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan 48109, USA.

出版信息

J Clin Invest. 2010 Oct;120(10):3440-2. doi: 10.1172/JCI44786. Epub 2010 Sep 27.

Abstract

Osteoporosis is a common, age-related bone disease that results from an imbalance between the processes of bone formation and bone resorption, resulting in reduced bone mass and increased risk of fracture. Mesenchymal stem cells have the capacity to differentiate into osteoblastic and adipogenic lineages; recent research suggests that the switch between these two fates may be key to the decreased bone density that occurs with aging. In this issue, Nishikawa et al. demonstrate that the basic leucine-zipper transcription factor Maf (also known as c-Maf) is central to osteoblast lineage commitment. In addition, they find that increased oxidative stress - as occurs with aging - decreases Maf expression. This work advances understanding of the transcriptional regulation of cell fate decisions and may help direct the development of new therapies to fight age-related bone loss.

摘要

骨质疏松症是一种常见的、与年龄相关的骨骼疾病,源于成骨和骨吸收过程之间的失衡,导致骨量减少和骨折风险增加。间充质干细胞具有分化为成骨细胞和脂肪细胞谱系的能力;最近的研究表明,这两种命运之间的转换可能是与衰老相关的骨密度降低的关键。在本期杂志中,Nishikawa 等人证明碱性亮氨酸拉链转录因子 Maf(也称为 c-Maf)是成骨细胞谱系决定的核心。此外,他们发现氧化应激增加——如衰老时发生的那样——会降低 Maf 的表达。这项工作推进了对细胞命运决定的转录调控的理解,并可能有助于指导开发新的治疗方法来对抗与年龄相关的骨质流失。

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