State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, Sichuan, China.
State Key Laboratory of Oral Diseases & National Center for Stomatology & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu 610041, Sichuan, China.
Int J Biochem Cell Biol. 2024 Feb;167:106507. doi: 10.1016/j.biocel.2023.106507. Epub 2023 Dec 23.
Zinc finger proteins (ZFPs) constitute a crucial group of transcription factors widely present in various organisms. They act as transcription factors, nucleases, and RNA-binding proteins, playing significant roles in cell differentiation, growth, and development. With extensive research on ZFPs, their roles in the determination of mesenchymal stem cells (MSCs) fate during osteogenic and adipogenic differentiation processes have become increasingly clear. ZFP521, for instance, is identified as an inhibitor of the Wnt signaling pathway and RUNX2's transcriptional activity, effectively suppressing osteogenic differentiation. Moreover, ZFP217 contributes to the inhibition of adipogenic differentiation by reducing the M6A level of the cell cycle regulator cyclin D1 (CCND1). In addition, other ZFPs can also influence the fate of mesenchymal stem cells (MSCs) during osteogenic and adipogenic differentiation through various signaling pathways, transcription factors, and epigenetic controls, participating in the subsequent differentiation and maturation of precursor cells. Given the prevalent occurrence of osteoporosis, obesity, and related metabolic disorders, a comprehensive understanding of the regulatory mechanisms balancing bone and fat metabolism is essential, with a particular focus on the fate determination of MSCs in osteogenic and adipogenic differentiation. In this review, we provide a detailed summary of how zinc finger proteins influence the osteogenic and adipogenic differentiation of MSCs through different signaling pathways, transcription factors, and epigenetic mechanisms. Additionally, we outline the regulatory mechanisms of ZFPs in controlling osteogenic and adipogenic differentiation based on various stages of MSC differentiation.
锌指蛋白(ZFPs)构成了转录因子的一个重要群体,广泛存在于各种生物体中。它们作为转录因子、核酸酶和 RNA 结合蛋白发挥作用,在细胞分化、生长和发育中起着重要作用。通过对 ZFPs 的广泛研究,它们在成骨和脂肪分化过程中决定间充质干细胞(MSCs)命运的作用变得越来越清楚。例如,ZFP521 被鉴定为 Wnt 信号通路和 RUNX2 转录活性的抑制剂,有效抑制成骨分化。此外,ZFP217 通过降低细胞周期调节剂 cyclin D1 (CCND1) 的 M6A 水平,有助于抑制脂肪分化。此外,其他 ZFPs 还可以通过各种信号通路、转录因子和表观遗传调控影响间充质干细胞(MSCs)在成骨和脂肪分化过程中的命运,参与前体细胞的后续分化和成熟。鉴于骨质疏松症、肥胖症和相关代谢紊乱的普遍发生,全面了解平衡骨和脂肪代谢的调节机制至关重要,特别关注 MSCs 在成骨和脂肪分化中的命运决定。在这篇综述中,我们详细总结了锌指蛋白如何通过不同的信号通路、转录因子和表观遗传机制影响 MSCs 的成骨和脂肪分化。此外,我们还根据 MSC 分化的不同阶段概述了 ZFPs 对成骨和脂肪分化的调控机制。