Mechanism of Interleukin-17A Regulation of Mesenchymal Stroma/Stem Cell Osteogenic Differentiation.

Juan F Santibanez
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Abstract

The immune and musculoskeletal systems closely interplay in bone repair and regeneration. After bone injury, the body produces high levels of cytokines and signaling molecules to balance bone formation and resorption. Interleukin (IL)-17A, a cytokine expressed early in the inflammatory process, profoundly influences osteoprogenitor cell fate, thereby contributing to bone homeostasis. In addition, mesenchymal stromal/stem cells (MSCs) can differentiate into osteoblasts, contributing to bone repair and regeneration. Although IL-17A can influence MSCs to become early osteoprogenitor cells, it also can inhibit bone formation. However, the reasons for these dual roles are not yet fully understood. This review overviews IL-17A signaling and the mechanisms that govern MSCs' osteogenic differentiation and summarizes relevant data from the literature on IL-17A's pro- and anti-osteogenic roles.

白细胞介素- 17a调控间充质间质/干细胞成骨分化的机制
免疫系统和肌肉骨骼系统在骨修复和再生中密切相互作用。骨损伤后,机体产生高水平的细胞因子和信号分子来平衡骨的形成和吸收。白细胞介素(IL)-17A是炎症过程早期表达的一种细胞因子,它深刻影响骨祖细胞的命运,从而促进骨稳态。此外,间充质基质/干细胞(MSCs)可以分化成成骨细胞,有助于骨修复和再生。虽然IL-17A可以影响MSCs成为早期的骨祖细胞,但它也可以抑制骨形成。然而,这些双重角色的原因还没有完全理解。本文综述了IL-17A信号通路及其调控间充质干细胞成骨分化的机制,并总结了IL-17A促进和抑制成骨作用的相关文献。
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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