Cao Zhentang, Wu Yufeng, Liu Genliang, Jiang Ying, Wang Xuemei, Wang Zhan, Feng Tao
Center for Neurodegenerative Disease, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China; China National Clinical Research Center for Neurological Diseases, Beijing, China.
Clinical Laboratory, Peking University Third Hospital, Peking University, Beijing, China; Department of Pathology, Peking University School of Basic Medical Sciences, Peking University, Beijing, China; Beijing Key Laboratory of Research and Transformation on Neurodegenerative Diseases Biomarkers, Beijing, China.
Neurosci Lett. 2019 Mar 23;696:114-120. doi: 10.1016/j.neulet.2018.12.030. Epub 2018 Dec 21.
Detection of α-synuclein (α-syn) in biological fluids such as saliva may serve as potential biomarker of PD. α-syn pertaining to extracellular vesicles (EVs) has been recently studied in plasma, but not in other biological fluids such as saliva.
Saliva samples were obtained from 74 PD and 60 healthy controls (HCs). The EVs were extracted from saliva by XYCQ EV Enrichment KIT. Western blot and Nanosight 300 were used to validate the existence of exosomes in EVs and to analyze the size of salivary EVs. Salivary EVs α-syn levels, including total α-syn (α-syn), oligomeric α-syn (α-syn) and phosphorylated-ser129 α-syn (α-syn), were measured by Electrochemiluminescence (ECL) assays. Diagnostic value and clinical relevance of salivary EVs α-syn were assessed by Receiver Operator Characteristic (ROC) curve and Spearman correlation.
Alix and CD9 positive EVs, representing the presence of exosomes, was detected in PD salivary samples. Size of salivary EVs was about 30-400 nm. The levels of α-syn and α-syn/α-syn in the salivary EVs were higher in PD than in HCs (10.39 ± 1.46 pg/ng vs.1.37 ± 0.24 pg/ng, p<0.001;1.70 ± 0.52 pg/ng vs.0.67 ± 0.26 pg/ng, p<0.001). There was no significant difference in α-syn、α-syn、 α-syn/α-syn ratio between PD and HCs (P = 0.723, 0.634, 0.734, respectively). α-syn 2.05 pg/ng distinguished PD from HCs with sensitivity 92% and specificity 86%; α-syn /α-syn 0.18 pg/ng differentiated PD from HCs with sensitivity 81% and specificity 71%. No significant correlation between salivary EVs α-syn, α-syn/α-syn and disease severity was found.
Exosomes are present in PD saliva. The α-syn and α-syn/α-syn ratio in salivary EVs may serve as potential diagnostic biomarkers for PD.
在唾液等生物体液中检测α-突触核蛋白(α-syn)可能作为帕金森病(PD)的潜在生物标志物。与细胞外囊泡(EVs)相关的α-syn最近已在血浆中进行研究,但尚未在唾液等其他生物体液中进行研究。
1)研究帕金森病患者唾液中外泌体的存在情况;2)探讨唾液细胞外囊泡中α-syn作为帕金森病潜在生物标志物的价值。
收集74例帕金森病患者和60例健康对照(HCs)的唾液样本。采用XYCQ EV富集试剂盒从唾液中提取细胞外囊泡。使用蛋白质免疫印迹法和纳米可视300对细胞外囊泡中外泌体的存在进行验证,并分析唾液细胞外囊泡的大小。通过电化学发光(ECL)测定法测量唾液细胞外囊泡α-syn水平,包括总α-syn(α-syn)、寡聚α-syn(α-syn)和磷酸化丝氨酸129α-syn(α-syn)。通过受试者工作特征(ROC)曲线和Spearman相关性评估唾液细胞外囊泡α-syn的诊断价值和临床相关性。
在帕金森病患者的唾液样本中检测到代表外泌体存在的Alix和CD9阳性细胞外囊泡。唾液细胞外囊泡的大小约为30 - 400nm。帕金森病患者唾液细胞外囊泡中α-syn和α-syn/α-syn的水平高于健康对照(分别为10.39±1.46pg/ng vs.1.37±0.24pg/ng,p<0.001;1.70±0.52pg/ng vs.0.67±0.26pg/ng,p<0.001)。帕金森病患者和健康对照之间α-syn、α-syn、α-syn/α-syn比值无显著差异(P分别为0.723、0.634、0.734)。α-syn 2.05pg/ng区分帕金森病患者和健康对照的敏感性为92%,特异性为86%;α-syn /α-syn 0.18pg/ng区分帕金森病患者和健康对照的敏感性为81%,特异性为71%。未发现唾液细胞外囊泡α-syn、α-syn/α-syn与疾病严重程度之间存在显著相关性。
帕金森病患者唾液中存在外泌体。唾液细胞外囊泡中的α-syn和α-syn/α-syn比值可能作为帕金森病的潜在诊断生物标志物。