Obstetrical Department, the First People's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology, No.157 Jinbi Road, Kunming, Yunnan, 650032, China.
Obstetrical Department, the First People's Hospital of Yunnan Province, the Affiliated Hospital of Kunming University of Science and Technology, No.157 Jinbi Road, Kunming, Yunnan, 650032, China.
Int Immunopharmacol. 2024 Mar 10;129:111626. doi: 10.1016/j.intimp.2024.111626. Epub 2024 Feb 5.
Gestational diabetes mellitus (GDM) is associated with adverse myocardial remodeling and impaired cardiac function of fetus. Nevertheless, specific molecular mechanisms underlying type 1 GDM-induced fetal myocardial injury remain unknown. Therefore, this study proposes to identify possible molecular mechanisms using RNA-seq.
A rat type 1 GDM model was developed using streptozotocin (STZ) (25 and 50 mg/kg), and weight and glucose tolerance of maternal and offspring were evaluated. Changes in markers of myocardial injury and oxidative stress identified by ELISA and biochemical kits in offspring hearts. Identification of differentially expressed mRNAs (DE-mRNAs) associated with myocardial injury in type 1 GDM offspring using RNA-seq. Proliferation, apoptosis, and oxidative stress were assessed in high glucose-induced H9C2 cells after exogenously modulating ATP Synthase Membrane Subunit E (ATP5me).
Maternal weight, glucose and glucose tolerance, and fetal weight and heart weight were reduced in the type 1 GDM model, especially in 50 mg/kg STZ-induced. Increased of creatine kinase-MB (CK-MB), cardiac troponin T (cTnT), hypersensitive C-reactive protein (hs-CRP), reactive oxygen species (ROS) and malondialdehyde (MDA) and decreased of superoxide dismutase (SOD) were observed in type 1 GDM offspring hearts. type 1 GDM offspring hearts exhibited disorganized cardiomyocytes with enlarged gaps, broken myocardial fibers, erythrocyte accumulation and inflammatory infiltration. RNA-seq identified 462 DE-mRNAs in type 1 GDM offspring hearts, which mainly regulate immunity, redox reactions, and cellular communication. Atp5me was under-expressed in type 1 GDM offspring hearts, and high glucose decreased Atp5me expression in H9C2 cells. Overexpressing Atp5me alleviated high glucose-induced decrease in proliferation, mitochondrial membrane potential, BCL2 and SOD, and increase in apoptosis, MDA, ROS, c-Caspase-3, and BAX in H9C2 cells.
This study first demonstrated that ATP5me attenuated type 1 GDM-induced fetal myocardial injury. This provides a possible molecular mechanism for the treatment of type 1 GDM-induced fetal myocardial injury.
妊娠糖尿病(GDM)与胎儿不良心肌重构和心功能受损有关。然而,1 型 GDM 引起胎儿心肌损伤的具体分子机制尚不清楚。因此,本研究拟采用 RNA-seq 技术来鉴定可能的分子机制。
采用链脲佐菌素(STZ)(25 和 50mg/kg)建立 1 型 GDM 大鼠模型,评估母鼠和仔鼠的体重和葡萄糖耐量。采用 ELISA 和生化试剂盒检测仔鼠心脏中心肌损伤和氧化应激标志物的变化。采用 RNA-seq 技术鉴定 1 型 GDM 仔鼠心脏中与心肌损伤相关的差异表达 mRNA(DE-mRNA)。用外源性调节 ATP 合酶膜亚基 E(ATP5me)后,评估高糖诱导的 H9C2 细胞的增殖、凋亡和氧化应激。
1 型 GDM 模型中,母鼠体重、血糖和葡萄糖耐量以及仔鼠体重和心脏重量均降低,尤其是在 50mg/kg STZ 诱导时。1 型 GDM 仔鼠心脏中肌酸激酶同工酶-MB(CK-MB)、心肌肌钙蛋白 T(cTnT)、超敏 C 反应蛋白(hs-CRP)、活性氧(ROS)和丙二醛(MDA)升高,超氧化物歧化酶(SOD)降低。1 型 GDM 仔鼠心脏表现出心肌细胞排列紊乱,间隙增大,心肌纤维断裂,红细胞堆积,炎症浸润。RNA-seq 鉴定出 1 型 GDM 仔鼠心脏中有 462 个 DE-mRNA,主要调节免疫、氧化还原反应和细胞通讯。1 型 GDM 仔鼠心脏中 Atp5me 表达下调,高糖降低 H9C2 细胞中 Atp5me 的表达。过表达 Atp5me 可减轻高糖诱导的 H9C2 细胞增殖减少、线粒体膜电位降低、BCL2 和 SOD 降低以及凋亡增加、MDA、ROS、c-Caspase-3 和 BAX 升高。
本研究首次证明 ATP5me 可减轻 1 型 GDM 引起的胎儿心肌损伤。这为治疗 1 型 GDM 引起的胎儿心肌损伤提供了一种可能的分子机制。