犬尿氨酸
间质细胞
骨髓
犬尿氨酸途径
吲哚胺2,3-双加氧酶
自噬
骨质疏松症
衰老
干细胞
生物
细胞生物学
成骨细胞
间充质干细胞
表型
癌症研究
免疫学
医学
内分泌学
色氨酸
生物化学
体外
氨基酸
细胞凋亡
基因
作者
Dhara Patel,Matthew L. Potter,Jordan Marcano Anaya,Meghan E. McGee‐Lawrence,Mark W. Hamrick,William Hill,Carlos M. Isales,Sadanand Fulzele
标识
DOI:10.1016/j.mad.2021.111464
摘要
Advanced age is one of the important contributing factors for musculoskeletal deterioration. Although the exact mechanism behind this degeneration is unknown, it has been previously established that nutritional signaling plays a vital role in musculoskeletal pathophysiology. Our group established the vital role of the essential amino acid, tryptophan, in aging musculoskeletal health. With advanced age, inflammatory factors activate indoleamine 2,3-dioxygenase (IDO1) and accumulate excessive intermediate tryptophan metabolites such as Kynurenine (KYN). With age, Kynurenine accumulates and suppresses osteogenic differentiation, impairs autophagy, promotes early senescence, and alters cellular bioenergetics of bone marrow stem cells. Recent studies have shown that Kynurenine negatively impacts bone marrow stromal cells (BMSCs) and, consequently, promotes bone loss. Overall, understanding the mechanism behind BMSCs losing their ability for osteogenic differentiation can provide insight into the prevention of osteoporosis and the development of targeted therapies. Therefore, in this article, we review Kynurenine and how it plays a vital role in BMSC dysfunction and bone loss with age.
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