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机械拉伸通过激活 RhoA/ROCK 通路诱导纤维环细胞衰老。

Mechanical Stretch Induces Annulus Fibrosus Cell Senescence through Activation of the RhoA/ROCK Pathway.

机构信息

Weifang People's Hospital, Weifang, Shandong, China.

Department of Orthopaedics, The Third People's Hospital of Jinan, Shandong, China.

出版信息

Biomed Res Int. 2021 Nov 19;2021:5321121. doi: 10.1155/2021/5321121. eCollection 2021.

Abstract

BACKGROUND

Intervertebral disc is responsible for absorbing and transmitting mechanical compression. Under physiological conditions, the peripheral annulus fibrosus (AF) cells are subjected to different magnitudes of transverse mechanical stretch depending on the swelling of the central nucleus pulposus tissue. However, the biological behavior of AF cells under mechanical stretch is not well studied.

OBJECTIVE

This study was performed to study the effects of mechanical tension on AF cell senescence and the potential signaling transduction pathway.

METHODS

Rat AF cells were made to experience different magnitudes of mechanical stretch (2% elongation and 20% elongation for 4 hours every day at 1 Hz) in a 10-day experiment period. The inhibitor RKI-1447 of the Rho-associated coiled-coil-containing protein kinases (ROCK) was added along with culture medium to investigate its role. Cell proliferation, cell cycle, telomerase activity, and expression of senescence markers (p16 and p53) were analyzed.

RESULTS

We found that 20% elongation significantly decreased cell proliferation, promoted G0/G1 cell cycle arrest, decreased telomerase activity, and upregulated mRNA/protein expression of p16 and p53. Moreover, the inhibitor RKI-1447 partly resisted effects of 20% elongation on these parameters of cell senescence.

CONCLUSION

High mechanical stretch obviously induces AF cell senescence through the RhoA/ROCK pathway. This study provides us a deeper understanding on the AF cell's behavior under mechanical stretch.

摘要

背景

椎间盘负责吸收和传递机械压缩。在生理条件下,周围的纤维环(AF)细胞会根据中央核髓组织的肿胀而受到不同大小的横向机械拉伸。然而,AF 细胞在机械拉伸下的生物学行为尚未得到很好的研究。

目的

本研究旨在研究机械张力对 AF 细胞衰老的影响及其潜在的信号转导途径。

方法

在 10 天的实验期间,每天以 1 Hz 的频率对大鼠 AF 细胞施加不同大小的机械拉伸(2%伸长和 20%伸长,每次持续 4 小时)。添加 Rho 相关卷曲螺旋蛋白激酶(ROCK)抑制剂 RKI-1447 与培养基一起培养,以研究其作用。分析细胞增殖、细胞周期、端粒酶活性以及衰老标志物(p16 和 p53)的表达。

结果

我们发现 20%的伸长明显降低了细胞增殖,促进了 G0/G1 细胞周期阻滞,降低了端粒酶活性,并上调了 p16 和 p53 的 mRNA/蛋白表达。此外,抑制剂 RKI-1447 部分抵抗了 20%伸长对这些衰老细胞参数的影响。

结论

高机械拉伸通过 RhoA/ROCK 途径明显诱导 AF 细胞衰老。本研究为我们深入了解 AF 细胞在机械拉伸下的行为提供了依据。

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