Lu Tang , Chengjie Yang , Yanhua Peng , Mudi Liu , Na Wei , Xin Fan , Bo Yang , Jing Jia , Ye Chen , Jianguo Feng , Jun Zhou
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This study aimed to investigate the regulatory role of YAP in ALI and ferroptosis caused by II/R, and to explore whether YAP exerts anti-ferroptosis and anti-inflammatory effects by promoting nuclear factor erythroid 2-related factor 2 (Nrf2) nuclear entry and upregulating Nrf2 expression. In vivo models demonstrated that overexpression of YAP inhibited II/R-induced ALI and ferroptosis. This was evident through the upregulation of glutathione peroxidase 4 (GPX4), solute carrier family 7 member 11 (SLC7A11), and Nrf2 expression, as well as the mitigation of characteristic mitochondrial ferroptosis changes in lung type II epithelial cells. Additionally, YAP overexpression protected against II/R-induced ALI in mice, leading to notable improvements in lung pathology, reduced pulmonary edema, and decreased lung inflammation. Consistent conclusions were also reached in vitro models. It was observed that overexpression of YAP inhibited ferroptosis and oxidative stress by increasing Nrf2 expression and promoting its nuclear translocation. Additionally, it was discovered that knocking down Nrf2 resulted in the abolition of YAP-mediated ferroptosis alleviation in MLE-12 cells. Based on our findings, we can infer that YAP inhibits ferroptosis by upregulating Nrf2 expression and promoting its translocation into the nucleus, thereby ameliorating oxidative stress and lung injury along with the systemic inflammatory response following II/R. 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引用次数: 0
摘要
肠缺血再灌注损伤(II/R)是一种常见的高发病率和死亡率的危重疾病。II/ r诱导的急性肺损伤(ALI)机制尚未完全阐明。Yes-associated protein (YAP)是Hippo信号通路的下游转录辅激活因子,在控制器官发育和细胞增殖中起核心作用。然而,YAP是否参与调控II/ r诱导的ALI仍有待进一步探讨。本研究旨在探讨YAP在II/R引起的ALI和铁下沉中的调节作用,并探讨YAP是否通过促进核因子红细胞2相关因子2 (Nrf2)的核进入和上调Nrf2的表达来发挥抗铁下沉和抗炎作用。体内模型显示,过表达YAP可抑制II/ r诱导的ALI和铁下垂。这可以通过上调谷胱甘肽过氧化物酶4 (GPX4)、溶质载体家族7成员11 (SLC7A11)和Nrf2的表达,以及减轻肺II型上皮细胞线粒体铁下垂的特征性变化来证明。此外,YAP过表达对小鼠II/ r诱导的ALI有保护作用,导致肺病理显著改善,肺水肿减少,肺部炎症减少。在体外模型中也得出了一致的结论。研究发现,过表达YAP通过增加Nrf2的表达和促进其核易位来抑制铁下垂和氧化应激。此外,研究发现,敲除Nrf2可导致MLE-12细胞中yap介导的铁下垂缓解消失。根据我们的研究结果,我们可以推断YAP通过上调Nrf2表达并促进其向细胞核转运,从而改善II/R后的氧化应激和肺损伤以及全身炎症反应,从而抑制铁下沉。此外,我们提出靶向YAP可能是通过抑制铁下垂治疗ALI的一种有希望的方法。
YAP/Nrf2 suppresses ferroptosis to alleviate acute lung injury induced by intestinal ischemia/reperfusion
Intestinal ischemia reperfusion (II/R) injury is a common critical disease with high morbidity and mortality. The mechanism of II/R-induced acute lung injury (ALI) is not fully elucidated. Yes-associated protein (YAP), a downstream transcriptional coactivator of the Hippo signaling pathway, plays a central role in controlling organ development and cell proliferation. However, whether YAP is involved in regulating II/R-induced ALI remains to be further explored. This study aimed to investigate the regulatory role of YAP in ALI and ferroptosis caused by II/R, and to explore whether YAP exerts anti-ferroptosis and anti-inflammatory effects by promoting nuclear factor erythroid 2-related factor 2 (Nrf2) nuclear entry and upregulating Nrf2 expression. In vivo models demonstrated that overexpression of YAP inhibited II/R-induced ALI and ferroptosis. This was evident through the upregulation of glutathione peroxidase 4 (GPX4), solute carrier family 7 member 11 (SLC7A11), and Nrf2 expression, as well as the mitigation of characteristic mitochondrial ferroptosis changes in lung type II epithelial cells. Additionally, YAP overexpression protected against II/R-induced ALI in mice, leading to notable improvements in lung pathology, reduced pulmonary edema, and decreased lung inflammation. Consistent conclusions were also reached in vitro models. It was observed that overexpression of YAP inhibited ferroptosis and oxidative stress by increasing Nrf2 expression and promoting its nuclear translocation. Additionally, it was discovered that knocking down Nrf2 resulted in the abolition of YAP-mediated ferroptosis alleviation in MLE-12 cells. Based on our findings, we can infer that YAP inhibits ferroptosis by upregulating Nrf2 expression and promoting its translocation into the nucleus, thereby ameliorating oxidative stress and lung injury along with the systemic inflammatory response following II/R. Furthermore, we propose that targeting YAP could be a promising approach for the treatment of ALI by suppressing ferroptosis.
期刊介绍:
Redox Biology is the official journal of the Society for Redox Biology and Medicine and the Society for Free Radical Research-Europe. It is also affiliated with the International Society for Free Radical Research (SFRRI). This journal serves as a platform for publishing pioneering research, innovative methods, and comprehensive review articles in the field of redox biology, encompassing both health and disease.
Redox Biology welcomes various forms of contributions, including research articles (short or full communications), methods, mini-reviews, and commentaries. Through its diverse range of published content, Redox Biology aims to foster advancements and insights in the understanding of redox biology and its implications.