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首页> 外文期刊>International journal of biological sciences >Alveolar type ii cells escape stress failure caused by tonic stretch through transient focal adhesion disassembly
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Alveolar type ii cells escape stress failure caused by tonic stretch through transient focal adhesion disassembly

机译:肺泡ii型细胞通过暂时性粘着性粘连分解而避免了由于张力扩张引起的应力衰竭

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Mechanical ventilation-induced excessive stretch of alveoli is reported to induce cellular stress failure and subsequent lung injury, and is therefore an injurious factor to the lung. Avoiding cellular stress failure is crucial to ventilator-induced lung injury (VILI) treatment. In the present study, primary rat alveolar type II (ATII) cells were isolated to evaluate their viability and the mechanism of their survival under tonic stretch. By the annexin V/ PI staining and flow cytometry assay, we demonstrated that tonic stretch-induced cell death is an im-mediate injury of mechanical stress. In addition, immunofluorescence and immunoblots assay showed that the cells experienced an expansion-contraction-reexpansion process, accom-panied by partial focal adhesion (FA) disassembly during contraction. Manipulation of integrin adherent affinity by altering bivalent cation levels in the culture medium and applying an in-tegrin neutralizing antibody showed that facilitated adhesion affinity promoted cell death under tonic stretch, while lower level of adhesion protected the cells from stretch-induced stress failure. Finally, a simplified numerical model was established to reveal that adequate disassembly of FAs reduced the forces transmitting throughout the cell. Taken together, these results indicate that ATII cells escape stress failure caused by tonic stretch via active cell morphological remodeling, during which cells transiently disassemble FAs to unload me-chanical forces.
机译:据报道,机械通气引起的肺泡过度拉伸会引起细胞应力衰竭和随后的肺损伤,因此是对肺的伤害因素。避免细胞应力衰竭对于呼吸机诱发的肺损伤(VILI)治疗至关重要。在本研究中,分离了大鼠原发性II型肺泡细胞(ATII),以评估其生存力以及在张力拉伸下的存活机制。通过膜联蛋白V / PI染色和流式细胞仪测定,我们证明了滋补拉伸诱导的细胞死亡是机械应力的直接伤害。此外,免疫荧光和免疫印迹测定表明,细胞经历了扩张-收缩-再扩张过程,伴随着收缩过程中的局部粘着斑(FA)分解。通过改变培养基中的二价阳离子水平并应用整合素中和抗体来操纵整合素粘附亲和力表明,促进粘附亲和力促进了张力拉伸下的细胞死亡,而较低水平的粘附力则保护了细胞免受拉伸诱导的应力衰竭。最后,建立了简化的数值模型以揭示FA的充分分解会减少传递到整个细胞的力。两者合计,这些结果表明,ATII细胞通过活跃的细胞形态重塑逃避了由张力扩展引起的应力衰竭,在此过程中,细胞会瞬时分解FAs从而释放机械力。

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