Shen Liming, Feng Chengyun, Zhang Kaoyuan, Chen Youjiao, Gao Yan, Ke Junyan, Chen Xinqian, Lin Jing, Li Cuihua, Iqbal Javed, Zhao Yuxi, Wang Weibin
College of Life Science and Oceanography, Shenzhen University, Shenzhen, China.
Maternal and Child Health Hospital of Baoan, Shenzhen, China.
Front Cell Neurosci. 2019 Mar 19;13:105. doi: 10.3389/fncel.2019.00105. eCollection 2019.
Autism is one of the most common neurological developmental disorder associated with social isolation and restricted interests in children. The etiology of this disorder is still unknown. There is neither any confirmed laboratory test nor any effective therapeutic strategy to diagnose or cure it. To search for biomarkers for early detection and exploration of the disease mechanisms, here, we investigated the protein expression signatures of peripheral blood mononuclear cells (PBMCs) in autistic children compared with healthy controls by using isobaric tags for relative and absolute quantitation (iTRAQ) proteomics approach. The results showed a total of 41 proteins as differentially expressed in autistic group as compared to control. These proteins are found associated with metabolic pathways, endoplasmic reticulum (ER) stress and protein folding, endocytosis, immune and inflammatory response, plasma lipoprotein particle organization, and cell adhesion. Among these, 17 proteins (13 up-regulated and four down-regulated) are found to be linked with mitochondria. Eight proteins including three already reported proteins in our previous studies were selected to be verified. Five already reported autism associated pro-inflammatory cytokines [interferon-γ (IFN-γ), interleukin-1β (IL-1β), IL-6, IL-12, and tumor necrosis factor-α (TNF-α)] were detected in plasma by enzyme-linked immunosorbent assay (ELISA) analysis. The results were consistent with proteomic results and reports from previous literature. These results proposed that PBMCs from autistic children might be activated, and ER stress, unfolded protein response (UPR), acute-phase response (APR), inflammatory response, and endocytosis may be involved in autism occurrence. These reported proteins may serve as potential biomarkers for early diagnosis of autism. More specifically, simultaneous detection of three proteins [complement C3 (C3), calreticulin (CALR), and SERPINA1] in the plasma and PBMCs could increase the authenticity of detection.
自闭症是儿童中最常见的神经发育障碍之一,与社交隔离和兴趣受限有关。这种疾病的病因仍然未知。既没有任何确诊的实验室检测方法,也没有任何有效的治疗策略来诊断或治愈它。为了寻找早期检测的生物标志物并探索疾病机制,在此,我们使用相对和绝对定量的等压标签(iTRAQ)蛋白质组学方法,研究了自闭症儿童外周血单核细胞(PBMC)与健康对照相比的蛋白质表达特征。结果显示,与对照组相比,自闭症组共有41种蛋白质差异表达。这些蛋白质与代谢途径、内质网(ER)应激和蛋白质折叠、内吞作用、免疫和炎症反应、血浆脂蛋白颗粒组织以及细胞粘附有关。其中,发现17种蛋白质(13种上调和4种下调)与线粒体有关。选择了8种蛋白质(包括我们之前研究中已报道的3种蛋白质)进行验证。通过酶联免疫吸附测定(ELISA)分析检测了血浆中5种已报道的与自闭症相关的促炎细胞因子[干扰素-γ(IFN-γ)、白细胞介素-1β(IL-1β)、IL-6、IL-12和肿瘤坏死因子-α(TNF-α)]。结果与蛋白质组学结果以及先前文献报道一致。这些结果表明,自闭症儿童的PBMC可能被激活,内质网应激、未折叠蛋白反应(UPR)、急性期反应(APR)、炎症反应和内吞作用可能参与自闭症的发生。这些报道的蛋白质可能作为自闭症早期诊断的潜在生物标志物。更具体地说,同时检测血浆和PBMC中的三种蛋白质[补体C3(C3)、钙网蛋白(CALR)和丝氨酸蛋白酶抑制剂A1(SERPINA1)]可以提高检测的可信度。