Department of Clinical Laboratory, Chinese PLA General Hospital, Beijing 100853, China.
Department of pediatrics, Chinese PLA General Hospital, Beijing 100853, China.
Clin Chim Acta. 2019 Dec;499:34-40. doi: 10.1016/j.cca.2019.08.027. Epub 2019 Aug 27.
Mucopolysaccharindosis type II (MPS II) is a rare lysosomal storage disorder caused by deficient or absent activity of the iduronate-2-sulfatase (IDS) enzyme, which leads to pathological accumulation of the glycosaminoglycans(GAGs). The absence of early diagnosis can result in irreversible developmental, neurological, and physiological damage. The lack of clear understanding of the etiology of physiological dysfunction in MPS II has been a major obstacle to the development of new treatment. Therefore, a reliable biomarker for early diagnosis and exploration of pathogenic mechanism are of great importance. Proteomics provides powerful tool for protein expression alterations and study of complicated pathological process. This study was performed to identify the differential protein profile in urine of MPS II patients using two-dimensional gel electrophoresis(2D-PAGE)combining with MALDI-TOF/TOF and a total of 15 differentially expressed proteins were identified. Content of alpha1-antitrypsin, Gm2 activator and lipocalin-type prostaglandin D synthase was measured by ELISA method. The value of urinary α1-AT/Cr in MPS II group was 0.79 ± 0.10 mg/mmol, significantly higher than 0.42 ± 0.05 mg/mmol in healthy control group; whereas the value of GM2A/Cr and L-PGDS/Cr in MPS II group was 1.30 ± 0.12 μg/mmol and 9.86 ± 1.16 ng/mmol respectively, which was significantly lower than 2.19 ± 0.19 μg/mmol and 13.98 ± 1.48 ng/mmol in healthy control group. The proteins can be considered as accessory diagnostic biomarkers for MPS II. This approach helped to discover early diagnostic markers and provided a better understanding of the pathogenic mechanism of MPS II.
黏多糖贮积症 II 型(MPS II)是一种罕见的溶酶体贮积症,由艾杜糖-2-硫酸酯酶(IDS)缺乏或缺失引起,导致糖胺聚糖(GAGs)的病理性积累。如果早期诊断不及时,可能会导致不可逆转的发育、神经和生理损伤。由于对 MPS II 生理功能障碍的发病机制缺乏清晰的认识,这一直是开发新疗法的主要障碍。因此,寻找可靠的早期诊断标志物和探索发病机制对于 MPS II 具有重要意义。蛋白质组学为蛋白质表达变化和复杂病理过程的研究提供了强大的工具。本研究采用二维凝胶电泳(2D-PAGE)联合 MALDI-TOF/TOF 技术,对 MPS II 患者尿液中的差异蛋白谱进行了分析,共鉴定出 15 种差异表达蛋白。采用 ELISA 法检测尿液中α1-抗胰蛋白酶、GM2 激活剂和脂联素型前列腺素 D 合酶的含量。MPS II 组尿α1-AT/Cr 值为 0.79±0.10mg/mmol,明显高于健康对照组的 0.42±0.05mg/mmol;而 MPS II 组 GM2A/Cr 和 L-PGDS/Cr 值分别为 1.30±0.12μg/mmol 和 9.86±1.16ng/mmol,明显低于健康对照组的 2.19±0.19μg/mmol 和 13.98±1.48ng/mmol。这些蛋白可以作为 MPS II 的辅助诊断生物标志物。该方法有助于发现早期诊断标志物,并为了解 MPS II 的发病机制提供了更好的认识。