Unraveling the dynamics of osteoblast differentiation in MC3T3-E1 cells: Transcriptomic insights into matrix mineralization and cell proliferation

IF 3.6 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Bone Pub Date : 2025-03-01 DOI:10.1016/j.bone.2025.117442
Heein Yoon , Seung Gwa Park , Hye-Rim Shin , Ki-Tae Kim , Young-Dan Cho , Jae-I Moon , Woo-Jin Kim , Hyun-Mo Ryoo
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Abstract

Unraveling the intricacies of osteoblast differentiation is crucial for advancing our comprehension of bone biology. This study investigated the complicated molecular events orchestrating osteoblast differentiation in MC3T3-E1 cells, a well-established in vitro culture model. Employing longitudinal RNA-sequencing analysis, we explored transcriptomic changes at the pivotal time points of 0, 1, 4, 7, 10, 14, and 21 days and categorized osteogenic differentiation into proliferation, matrix maturation, and mineralization stages. Notably, we observed a simultaneous increase in matrix mineralization and cell proliferation during the mineralization stage, accompanied by a positive correlation between proliferation-associated genes and those enriched in ossification. Additionally, we identified the presence of proliferating cells over the mineralizing matrix layers. These results could serve as a model for understanding the principles by which bone lining cells are formed on the calcified bone matrix and the mechanism by which new osteoblasts are recruited during the bone remodeling process.
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揭示 MC3T3-E1 细胞成骨细胞分化的动态过程:从转录组深入了解基质矿化和细胞增殖
揭示成骨细胞分化的复杂性对于提高我们对骨生物学的理解至关重要。本研究研究了MC3T3-E1细胞成骨分化的复杂分子事件,这是一种成熟的体外培养模型。通过纵向rna测序分析,我们探索了0、1、4、7、10、14和21天关键时间点的转录组学变化,并将成骨分化分为增殖、基质成熟和矿化阶段。值得注意的是,在矿化阶段,我们观察到基质矿化和细胞增殖同时增加,并伴有增殖相关基因与骨化富集基因之间的正相关。此外,我们发现在矿化基质层上存在增殖细胞。这些结果可以作为理解骨衬里细胞在钙化骨基质上形成的原理和骨重塑过程中新成骨细胞募集的机制的模型。
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来源期刊
Bone
Bone 医学-内分泌学与代谢
CiteScore
8.90
自引率
4.90%
发文量
264
审稿时长
30 days
期刊介绍: BONE is an interdisciplinary forum for the rapid publication of original articles and reviews on basic, translational, and clinical aspects of bone and mineral metabolism. The Journal also encourages submissions related to interactions of bone with other organ systems, including cartilage, endocrine, muscle, fat, neural, vascular, gastrointestinal, hematopoietic, and immune systems. Particular attention is placed on the application of experimental studies to clinical practice.
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