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周期性热应激通过激活YAP信号通路使间充质干细胞向成骨细胞分化。

Periodic Heat Stress Licenses EMSC Differentiation into Osteoblasts via YAP Signaling Pathway Activation.

作者信息

Shi Wentao, Wang Zhe, Bian Lu, Wu Yiqing, HuiYa Mei, Zhou Yanjun, Zhang Zhijian, Wang Qing, Zhao Peng, Lu Xiaojie

机构信息

Jiangnan University Affiliated Hospital, Wuxi, Jiangsu Province 214122, China.

School of Medicine, Jiangsu University, Zhenjiang, Jiangsu Province 212001, China.

出版信息

Stem Cells Int. 2022 Mar 18;2022:3715471. doi: 10.1155/2022/3715471. eCollection 2022.

Abstract

BACKGROUND

The repair and regeneration of large bone defects represent highly challenging tasks in bone tissue engineering. Although recent studies have shown that osteogenesis is stimulated by periodic heat stress, the thermal regulation of osteogenic differentiation in ectomesenchymal stem cells (EMSCs) is not well studied.

METHODS AND RESULTS

In this study, the direct effects of periodic heat stress on the differentiation of EMSCs into osteoblasts were investigated. EMSCs derived from rat nasal respiratory mucosa were seeded onto culture plates, followed by 1 h of heat stress at 41°C every 7 days during osteogenic differentiation. Based on the results of the present study, periodic heating increases alkaline phosphatase (ALP) activity, upregulates osteogenic-related proteins, and promotes EMSC mineralization. In particular, increased YAP nuclear translocation and YAP knockdown inhibited osteogenic differentiation induced by heat stress. Furthermore, the expression and activity of transglutaminase 2 (TG2) were significantly increased after YAP nuclear translocation.

CONCLUSION

Together, these results indicate that YAP plays a key role in regulating cellular proteostasis under stressful cellular conditions by modulating the TG2 response.

摘要

背景

大骨缺损的修复和再生是骨组织工程中极具挑战性的任务。尽管最近的研究表明周期性热应激可刺激成骨作用,但外间充质干细胞(EMSCs)中成骨分化的热调节尚未得到充分研究。

方法与结果

在本研究中,研究了周期性热应激对EMSCs向成骨细胞分化的直接影响。将源自大鼠鼻呼吸黏膜的EMSCs接种到培养板上,在成骨分化过程中每7天进行1小时41°C的热应激处理。根据本研究结果,周期性加热可增加碱性磷酸酶(ALP)活性,上调成骨相关蛋白,并促进EMSCs矿化。特别是,YAP核转位增加和YAP敲低抑制了热应激诱导的成骨分化。此外,YAP核转位后转谷氨酰胺酶2(TG2)的表达和活性显著增加。

结论

总之,这些结果表明YAP通过调节TG2反应在应激细胞条件下调节细胞蛋白质稳态中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57ba/8960005/bb8859e18993/SCI2022-3715471.002.jpg

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