Department of Nephrology, Institute of Nephrology and Blood Purification, The First Affiliated Hospital of Jinan University, Guangzhou, China; China Clinical Medical Research Center, Guangdong Provincial Engineering Research Center of Autoimmune Disease Precision Medicine, Shenzhen Engineering Research Center of Autoimmune Disease, The Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen, China.
China Clinical Medical Research Center, Guangdong Provincial Engineering Research Center of Autoimmune Disease Precision Medicine, Shenzhen Engineering Research Center of Autoimmune Disease, The Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen, China.
J Proteomics. 2023 Sep 15;287:104977. doi: 10.1016/j.jprot.2023.104977. Epub 2023 Jul 22.
Primary Sjogren's Syndrome (pSS) is a chronic autoimmune disease, with unclear pathogenies. Lysine-malonylation (Kmal) as a novel post-translational modification (PTMs) was found associated with metabolic, immune, and inflammatory processes. For purpose of investigating the proteomic profile and functions of kmal in pSS, liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based analysis and bioinformatics analysis are performed based on twenty-eight pSS patients versus twenty-seven healthy controls (HCs). A total of 331 down-regulated proteins and 289 up-regulated proteins are observed in differentially expressed proteins (DEPs) of pSS. We discover the expression of transforming growth factor beta-1 (TGFB1) and CD40 ligand downregulate which enriches in the inflammatory associated pathway. Expression of signal transducer and activator of transcription 1-alpha/beta (STAT1) show upregulation and enrich in type I interferon signaling pathway and IL-27-mediated signaling pathway. In differentially malonylated proteins (DMPs) of pSS, we identify 3 proteins are down-regulated in 7 sites and 18 proteins are up-regulated in 19 sites. Expression of malonylated integrin-linked kinase (ILK) significantly enrich in the focal adhesion pathway. Together, our data provide evidence that downregulation of TGFB1 and CD40LG play a critical role in the inflammatory process of pSS, while upregulation of STAT1 may be associated with IL-27 immunity and pSS immune dysfunction. Moreover, kmal modification at the kinase domain of ILK may destabilize ILK that thus contributing to pSS pathogenies by regulating the focal adhesion pathway. SIGNIFICANCE: Our research offered the first characterization of Kmal, a newly identified form of lysine acylation in pSS, as well as proteomic data on individuals with pSS. In this study, we found that several key DMPs were associated with focal adhesion pathway, which contributes to the development of pSS. The present results provide an informative dataset for the future exploration of Kmal in pSS.
原发性干燥综合征(pSS)是一种慢性自身免疫性疾病,其发病机制尚不清楚。赖氨酸丙二酰化(Kmal)作为一种新的翻译后修饰(PTMs),与代谢、免疫和炎症过程有关。为了研究 pSS 中 kmal 的蛋白质组特征和功能,我们对 28 名 pSS 患者和 27 名健康对照(HCs)进行了基于液相色谱-串联质谱(LC-MS/MS)的分析和生物信息学分析。在 pSS 的差异表达蛋白(DEPs)中观察到 331 个下调蛋白和 289 个上调蛋白。我们发现转化生长因子β-1(TGFB1)和 CD40 配体的表达下调,这丰富了与炎症相关的途径。信号转导和转录激活因子 1-α/β(STAT1)的表达上调,并在 I 型干扰素信号通路和 IL-27 介导的信号通路中富集。在 pSS 的差异丙二酰化蛋白(DMPs)中,我们确定 3 个蛋白在 7 个位点下调,18 个蛋白在 19 个位点上调。丙二酰化整合素连接激酶(ILK)的表达显著富集在粘着斑途径中。总之,我们的数据提供了证据,表明 TGFB1 和 CD40LG 的下调在 pSS 的炎症过程中起着关键作用,而 STAT1 的上调可能与 IL-27 免疫和 pSS 免疫功能障碍有关。此外,ILK 激酶结构域的 kmal 修饰可能会使 ILK 不稳定,从而通过调节粘着斑途径促进 pSS 的发病机制。意义:我们的研究首次对 pSS 中一种新发现的赖氨酸酰化形式 Kmal 以及个体的蛋白质组数据进行了描述。在这项研究中,我们发现几个关键的 DMPs 与粘着斑途径有关,这有助于 pSS 的发展。本研究结果为进一步探索 pSS 中 Kmal 提供了有价值的数据集。