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人牙囊细胞成骨分化过程中的磷酸化蛋白质组分析。

Analysis of the phosphoproteome in human dental follicle cells during osteogenic differentiation.

机构信息

Department of Oral and Maxillofacial Surgery, University Hospital Regensburg, Regensburg, Germany.

Department of Clinical Biochemistry and Pharmacology, Centre for Clinical Proteomics, Odense University Hospital, Odense, Denmark.

出版信息

Eur J Oral Sci. 2023 Oct-Nov;131(5-6):e12952. doi: 10.1111/eos.12952. Epub 2023 Sep 4.

Abstract

Dental follicle cells (DFCs) are osteogenic progenitor cells and are well suited for molecular studies of differentiation of alveolar osteoblasts. A recent study examined the metabolism in DFCs during osteogenic differentiation and showed that energy metabolism is increased after 14 days of differentiation (mid phase). However, previous studies have examined proteomes at early (2 h, 24 h) or very late (28 days) stages of differentiation, but not during the phase of increased metabolic activity. In this study, we examined the phosphoproteome at the mid phase (14 days) of osteogenic differentiation. Analysis of DFC phosphoproteomes showed that during this phase of osteogenic differentiation, proteins that are part of signal transduction are significantly regulated. Proteins involved in the regulation of the cytoskeleton and apoptosis were also increased in expression. As osteogenic differentiation induced oxidative stress and apoptosis in DFCs, the oxidative stress defense protein, catalase, was also upregulated during osteogenic differentiation, which supports the biomineralization of DFCs. In summary, this study revealed that during the middle phase (14 days) of osteogenic differentiation, processes in DFCs related to the control of cell organization, apoptosis, and oxidative stress are regulated.

摘要

牙滤泡细胞(DFCs)是成骨祖细胞,非常适合用于研究成骨细胞分化的分子机制。最近的一项研究检测了成骨分化过程中 DFCs 的代谢情况,结果表明在分化的第 14 天(中期)能量代谢增加。然而,以前的研究仅在分化的早期(2 小时、24 小时)或非常晚期(28 天)阶段检测了蛋白质组,而没有在代谢活性增加的阶段进行检测。在这项研究中,我们在成骨分化的中期(第 14 天)检测了 DFC 的磷酸化蛋白质组。对 DFC 磷酸化蛋白质组的分析表明,在成骨分化的这个阶段,参与信号转导的蛋白质受到明显的调控。参与细胞骨架和细胞凋亡调节的蛋白质的表达也增加了。由于成骨分化诱导 DFC 发生氧化应激和细胞凋亡,因此在成骨分化过程中,氧化应激防御蛋白——过氧化氢酶也被上调,这支持了 DFC 的生物矿化。总之,本研究揭示了在成骨分化的中期(14 天),与细胞组织、细胞凋亡和氧化应激控制相关的 DFC 过程受到调控。

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