Clinical Medical Research Center, Guangdong Clinical Medical Research Center of Birth Defects, the Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Jinan University, Shenzhen, Guangdong, China.
Institute of Nephrology and Blood Purification, the First Affiliated Hospital of Jinan University, Jinan University, Guangzhou, Guangdong, China.
Proteomics. 2022 Nov;22(22):e2200124. doi: 10.1002/pmic.202200124. Epub 2022 Sep 18.
Gestational diabetes mellitus (GDM) and preeclampsia (PE) are associated with maternal and infant health. Although the pathogenesis of PE and GDM remains controversial, oxidative stress is involved in the underlying pathology of GDM and PE. Protein lysine acetylation (Kac) plays an important regulatory role in biological processes. There is little data regarding the association of the maternal acetylome with GDM and PE. This study aimed to assess the potential value of the proteome and acetylome for GDM and PE. In our study, we included placental tissues from healthy individuals (n = 6), GDM patients (n = 6), and PE patients (n = 6) to perform 4D-label free quantification proteomics analysis and PRM analysis. We identified 22 significantly regulated proteins and 192 significantly regulated acetylated proteins between the GDM and PE groups. Furthermore, 192 significantly regulated acetylated proteins were mainly enriched in endoplasmic reticulum stress (ERS) and ferroptosis pathways. Seventeen acetylated sites in these two pathways were verified by PRM analysis. Our comprehensive analysis revealed key features of GDM/PE-significantly regulated acetylated proteins in the placentas from GDM and PE. The results of signaling pathway analysis focused on ERS and ferroptosis. These findings may help explore the underlying pathology, new biomarkers, and therapeutic targets of GDM and PE.
妊娠期糖尿病(GDM)和子痫前期(PE)与母婴健康有关。虽然 PE 和 GDM 的发病机制仍存在争议,但氧化应激参与了 GDM 和 PE 的潜在病理过程。蛋白赖氨酸乙酰化(Kac)在生物过程中发挥着重要的调节作用。关于母体乙酰组与 GDM 和 PE 的关联的数据很少。本研究旨在评估蛋白质组和乙酰组在 GDM 和 PE 中的潜在价值。在我们的研究中,我们纳入了来自健康个体(n=6)、GDM 患者(n=6)和 PE 患者(n=6)的胎盘组织,进行了 4D 无标记定量蛋白质组学分析和 PRM 分析。我们在 GDM 和 PE 组之间鉴定出 22 个显著调节的蛋白质和 192 个显著调节的乙酰化蛋白质。此外,192 个显著调节的乙酰化蛋白质主要富集在内质网应激(ERS)和铁死亡途径中。通过 PRM 分析验证了这两条通路中的 17 个乙酰化位点。我们的综合分析揭示了 GDM/PE 中胎盘显著调节的乙酰化蛋白质的关键特征。信号通路分析的结果集中在 ERS 和铁死亡上。这些发现可能有助于探索 GDM 和 PE 的潜在病理、新的生物标志物和治疗靶点。