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PHLDA3抑制通过激活PI3K/AKT信号通路减轻内质网应激诱导的心肌缺氧/复氧损伤中的细胞凋亡。

PHLDA3 inhibition attenuates endoplasmic reticulum stress-induced apoptosis in myocardial hypoxia/reoxygenation injury by activating the PI3K/AKT signaling pathway.

作者信息

Liu Kai, Chen Ying, Ai Fen, Li Yun-Qian, Zhang Kun, Zhang Wei-Tong

机构信息

Department of Geriatric Center, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, Hainan 570311, P.R. China.

Department of Emergency, The Central Hospital of Wuhan, Tongji Medical College, Hua Zhong University of Science and Technology, Wuhan, Hubei 430000, P.R. China.

出版信息

Exp Ther Med. 2021 Jun;21(6):613. doi: 10.3892/etm.2021.10045. Epub 2021 Apr 14.

Abstract

Endoplasmic reticulum stress (ERS)-induced apoptosis serves a crucial role in the pathogenesis of myocardial ischemia/reperfusion injury (MIRI). Previous studies have confirmed that pleckstrin homology-like domain family A member 3 (PHLDA3) is an important mediator in ERS-associated apoptosis. The aim of the current study focused on whether PHLDA3 served protective effects on hypoxia/reoxygenation (H/R)-injured cardiomyocytes by inhibiting ERS-induced apoptosis. Furthermore, the molecular mechanisms associated with the PI3K/AKT signaling pathway were investigated. Primary neonatal rat cardiomyocytes were isolated and randomized into four groups: i) Control + adenovirus encoding scrambled short hairpin RNA (AdshRNA); ii) control + adenoviral vectors encoding PHLDA3 shRNA (AdshPHLDA3); iii) H/R+ AdshRNA and iv) H/R+AdshPHLDA3. AdshPHLDA3 was used to knock down PHLDA3. An H/R injury model was constructed by treatment with hypoxia for 4 h followed by reoxygenation for 6 h. A PI3K/AKT inhibitor, LY294002, was supplemented in mechanistic studies. Cell viability and LDH/CK releases were detected to evaluate myocardial damage. Flow cytometry assays were used to assess apoptotic response. Western blotting assays were used to detect protein expression. The results demonstrated that H/R induced myocardial damage and increased PHLDA3 expression. ERS-induced apoptosis was significantly increased following H/R injury, as indicated by increased apoptotic rates and ERS-associated protein expression, including those of CHOP, 78 kDa glucose-regulated protein and caspase-12. However, PHLDA3 inhibition following AdshPHLDA3 transfection reversed cell damage and ERS-associated apoptosis on H/R injury. Studies for molecular mechanisms concluded that the apoptosis-inhibition effects and cardioprotective roles of PHLDA3 inhibition were induced partly by the activation of the PI3K/AKT pathway, which was verified by LY294002 treatment. In conclusion, in the process of H/R injury, PHLDA3 inhibition reduced ERS-induced apoptosis and H/R injury by activating the PI3K/AKT pathway. PHLDA3 may be a therapeutic target for the treatment of MIRI.

摘要

内质网应激(ERS)诱导的细胞凋亡在心肌缺血/再灌注损伤(MIRI)的发病机制中起关键作用。先前的研究证实,普列克底物蛋白同源结构域样家族A成员3(PHLDA3)是ERS相关细胞凋亡的重要介质。本研究的目的集中于PHLDA3是否通过抑制ERS诱导的细胞凋亡对缺氧/复氧(H/R)损伤的心肌细胞发挥保护作用。此外,还研究了与PI3K/AKT信号通路相关的分子机制。分离原代新生大鼠心肌细胞并随机分为四组:i)对照+编码乱序短发夹RNA的腺病毒(AdshRNA);ii)对照+编码PHLDA3 shRNA的腺病毒载体(AdshPHLDA3);iii)H/R + AdshRNA和iv)H/R + AdshPHLDA3。AdshPHLDA3用于敲低PHLDA3。通过缺氧处理4小时然后复氧6小时构建H/R损伤模型。在机制研究中补充了PI3K/AKT抑制剂LY294002。检测细胞活力和LDH/CK释放以评估心肌损伤。流式细胞术检测用于评估细胞凋亡反应。蛋白质印迹分析用于检测蛋白质表达。结果表明,H/R诱导心肌损伤并增加PHLDA3表达。H/R损伤后,ERS诱导的细胞凋亡显著增加,凋亡率和ERS相关蛋白表达增加,包括CHOP、78 kDa葡萄糖调节蛋白和半胱天冬酶-12的表达增加。然而,AdshPHLDA3转染后抑制PHLDA3可逆转H/R损伤对细胞的损伤和ERS相关的细胞凋亡。分子机制研究得出结论,PHLDA3抑制的抗凋亡作用和心脏保护作用部分是由PI3K/AKT途径的激活诱导的,LY294002处理验证了这一点。总之,在H/R损伤过程中,抑制PHLDA3可通过激活PI3K/AKT途径减少ERS诱导的细胞凋亡和H/R损伤。PHLDA3可能是治疗MIRI的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c7c/8082641/93f5077efaa9/etm-21-06-10045-g00.jpg

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