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Translational Research in Acute Lung Injury and Pulmonary Fibrosis: TRIM72 modulates caveolar endocytosis in repair of lung cells

机译:急性肺损伤和肺纤维化的转化研究:TRIM72调节肺泡内吞作用修复肺细胞

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摘要

Alveolar epithelial and endothelial cell injury is a major feature of the acute respiratory distress syndrome, in particular when in conjunction with ventilation therapies. Previously we showed [Kim SC, Kellett T, Wang S, Nishi M, Nagre N, Zhou B, Flodby P, Shilo K, Ghadiali SN, Takeshima H, Hubmayr RD, Zhao X. Am J Physiol Lung Cell Mol Physiol 307: L449–L459, 2014.] that tripartite motif protein 72 (TRIM72) is essential for amending alveolar epithelial cell injury. Here, we posit that TRIM72 improves cellular integrity through its interaction with caveolin 1 (Cav1). Our data show that, in primary type I alveolar epithelial cells, lack of TRIM72 led to significant reduction of Cav1 at the plasma membrane, accompanied by marked attenuation of caveolar endocytosis. Meanwhile, lentivirus-mediated overexpression of TRIM72 selectively increases caveolar endocytosis in rat lung epithelial cells, suggesting a functional association between these two. Further coimmunoprecipitation assays show that deletion of either functional domain of TRIM72, i.e., RING, B-box, coiled-coil, or PRY-SPRY, abolishes the physical interaction between TRIM72 and Cav1, suggesting that all theoretical domains of TRIM72 are required to forge a strong interaction between these two molecules. Moreover, in vivo studies showed that injurious ventilation-induced lung cell death was significantly increased in knockout (KO) TRIM72KO and Cav1KO lungs compared with wild-type controls and was particularly pronounced in double KO mutants. Apoptosis was accompanied by accentuation of gross lung injury manifestations in the TRIM72KO and Cav1KO mice. Our data show that TRIM72 directly and indirectly modulates caveolar endocytosis, an essential process involved in repair of lung epithelial cells through removal of plasma membrane wounds. Given TRIM72's role in endomembrane trafficking and cell repair, we consider this molecule an attractive therapeutic target for patients with injured lungs.
机译:肺泡上皮和内皮细胞损伤是急性呼吸窘迫综合征的主要特征,特别是与通气疗法结合使用时。先前,我们显示了[Kim SC,Kellett T,Wang S,Nishi M,Nagre N,Zhou B,Flodby P,Shilo K,Ghadiali SN,Takeshima H,Hubmayr RD,ZhaoX。AmPhysiol肺细胞Mol Physiol 307:L449 –L459,2014.]三方基序蛋白72(TRIM72)对于修正肺泡上皮细胞损伤至关重要。在这里,我们认为TRIM72通过与小窝蛋白1(Cav1)的相互作用改善了细胞的完整性。我们的数据显示,在主要的I型肺泡上皮细胞中,缺乏TRIM72导致质膜上Cav1的显着减少,并伴有小泡内吞作用的明显减弱。同时,慢病毒介导的TRIM72过表达选择性增加大鼠肺上皮细胞中的海绵状内吞作用,提示这两者之间存在功能关联。进一步的免疫共沉淀试验表明,删除TRIM72的任何功能域,即RING,B-box,卷曲螺旋或PRY-SPRY,都消除了TRIM72和Cav1之间的物理相互作用,这表明需要锻造TRIM72的所有理论域这两个分子之间有很强的相互作用。此外,体内研究表明,与野生型对照组相比,敲除(KO)TRIM72 KO 和Cav1 KO 肺中有害通气诱导的肺细胞死亡显着增加,并且在双KO突变体中特别明显。在TRIM72 KO 和Cav1 KO 小鼠中,细胞凋亡伴随着严重的肺损伤表现。我们的数据表明,TRIM72直接和间接调节小窝内吞作用,这是通过清除质膜伤口来修复肺上皮细胞的重要过程。考虑到TRIM72在内膜运输和细胞修复中的作用,我们认为该分子对于肺部受伤的患者是有吸引力的治疗靶标。

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