Primary Cilia Regulate the Homeostasis and Regeneration of the Stem Cell Niche in the Tooth

IF 4.5 2区 生物学 Q2 CELL BIOLOGY Journal of Cellular Physiology Pub Date : 2024-12-29 DOI:10.1002/jcp.31517
Xinming Zhang, Yuxin Cao, Mengge Wang, Yujia Li, Hanxiao Yin, Hua Ni, Song Yang, Fan Yu, Jia Yang, Lisu Peng, Meilin Hu, Dengwen Li, Dayong Liu
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Abstract

Primary cilia, functioning as crucial hubs for signal sensing and transduction, are integral to the development and maintenance of homeostasis across various organs. However, their roles in tooth homeostasis and repair remain inadequately understood. In this study, we reveal an indispensable role for primary cilia in regulating the homeostasis and regeneration of teeth, primarily through the regulation of cell proliferation. Using cilium-deficient mice, we demonstrate that disruption of ciliary homeostasis leads to abnormal tooth morphology, stunted growth and notably impaired tooth repair. RNA sequencing reveals a dysregulation in genes associated with various biological processes such as cell proliferation, differentiation, and cycle regulation. Furthermore, we show that cilium-deficient mice display reduced cell proliferation. Our findings highlight a critical function for primary cilia in the regulation of tooth homeostasis and regeneration and have important implications for the development of tooth regeneration therapies.

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初级纤毛调节牙齿干细胞生态位的动态平衡和再生。
初级纤毛作为信号感知和转导的关键枢纽,是各器官发展和维持体内平衡不可或缺的组成部分。然而,它们在牙齿平衡和修复中的作用仍然没有得到充分的了解。在这项研究中,我们揭示了初级纤毛在调节牙齿稳态和再生中不可或缺的作用,主要是通过调节细胞增殖。利用纤毛缺陷小鼠,我们证明了纤毛稳态的破坏会导致牙齿形态异常、生长迟缓和明显的牙齿修复受损。RNA测序揭示了与各种生物过程相关的基因失调,如细胞增殖、分化和周期调节。此外,我们发现纤毛缺陷小鼠显示细胞增殖减少。我们的研究结果强调了初级纤毛在调节牙齿动态平衡和再生中的关键功能,并对牙齿再生治疗的发展具有重要意义。
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来源期刊
CiteScore
14.70
自引率
0.00%
发文量
256
审稿时长
1 months
期刊介绍: The Journal of Cellular Physiology publishes reports of high biological significance in areas of eukaryotic cell biology and physiology, focusing on those articles that adopt a molecular mechanistic approach to investigate cell structure and function. There is appreciation for the application of cellular, biochemical, molecular and in vivo genetic approaches, as well as the power of genomics, proteomics, bioinformatics and systems biology. In particular, the Journal encourages submission of high-interest papers investigating the genetic and epigenetic regulation of proliferation and phenotype as well as cell fate and lineage commitment by growth factors, cytokines and their cognate receptors and signal transduction pathways that influence the expression, integration and activities of these physiological mediators. Similarly, the Journal encourages submission of manuscripts exploring the regulation of growth and differentiation by cell adhesion molecules in addition to the interplay between these processes and those induced by growth factors and cytokines. Studies on the genes and processes that regulate cell cycle progression and phase transition in eukaryotic cells, and the mechanisms that determine whether cells enter quiescence, proliferate or undergo apoptosis are also welcomed. Submission of papers that address contributions of the extracellular matrix to cellular phenotypes and physiological control as well as regulatory mechanisms governing fertilization, embryogenesis, gametogenesis, cell fate, lineage commitment, differentiation, development and dynamic parameters of cell motility are encouraged. Finally, the investigation of stem cells and changes that differentiate cancer cells from normal cells including studies on the properties and functions of oncogenes and tumor suppressor genes will remain as one of the major interests of the Journal.
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