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首页> 外文期刊>Biochemical and Biophysical Research Communications >Preconditioning effects of physiological cyclic stretch on pathologically mechanical stretch-induced alveolar epithelial cell apoptosis and barrier dysfunction
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Preconditioning effects of physiological cyclic stretch on pathologically mechanical stretch-induced alveolar epithelial cell apoptosis and barrier dysfunction

机译:生理循环拉伸对病理性机械拉伸诱导的肺泡上皮细胞凋亡和屏障功能障碍的预处理作用

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摘要

Background We aim to investigate the effects of preconditioning of physiological cyclic stretch on the alveolar epithelial cell apoptosis induced by pathologically mechanical stretch and barrier dysfunction and how these effects are linked to differential expression of small GTPases Rac and Rho mRNA. Methods Pulmonary alveolar epithelial cells were subjected to different treatments of cyclic stretch (CS) at 5% and 20% elongation, respectively. Cells maintained in normal cell culture were used as negative control. On the other hand, cell apoptosis and Rac/Rho activities in cells with or without preconditioning of physiologically relevant magnitudes of CS (5% CS) with different durations (0, 15, 30, 60 and 120 min) in prior to 6-h treatment with pathological CS stimulation (20% CS) were compared and measured. Results Pathological CS could cause a significant increase in apoptosis rate, which is considered to be associated with the repression of Rac mRNA and activation of Rho mRNA. In contrast, physiological 5%-CS preconditioning suppressed cell apoptosis and induced nearly complete monolayer recovery with fewer actin stress fibers and paracellular gap formation. Consistent with differential effects on cell apoptosis and epithelial cell integrity, physiological CS preconditioning enhanced expression of Rac mRNA but inhibited Rho activation. Conclusions Physiological CS preconditioning has an inhibitory effect on cell apoptosis while exerts a stimulatory impact on epithelial cell recovery via regulation of Rac and Rho activities.
机译:背景我们旨在研究生理循环拉伸的预处理对病理性机械拉伸和屏障功能障碍引起的肺泡上皮细胞凋亡的影响,以及这些作用如何与小GTPases Rac和Rho mRNA的差异表达相关。方法分别以5%和20%的伸长率对肺泡上皮细胞进行不同的循环拉伸(CS)处理。维持在正常细胞培养物中的细胞用作阴性对照。另一方面,在6小时之前的不同持续时间(0、15、30、60和120分钟)中,无论是否经过生理相关CS预处理(5%CS)的预处理,细胞的细胞凋亡和Rac / Rho活性比较并测量了病理性CS刺激(20%CS)治疗。结果病理性CS可能导致细胞凋亡率显着增加,这被认为与Rac mRNA的抑制和Rho mRNA的激活有关。相反,生理性5%-CS预处理可抑制细胞凋亡并诱导几乎完全的单层恢复,而肌动蛋白应激纤维和细胞旁间隙的形成较少。与对细胞凋亡和上皮细胞完整性的不同影响相一致,生理性CS预处理可增强Rac mRNA的表达,但抑制Rho激活。结论生理学CS预处理可通过调节Rac和Rho活性来抑制细胞凋亡,同时对上皮细胞的恢复产生刺激作用。

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