Significant modifications of the salivary proteome potentially associated with complications of Down syndrome revealed by top-down proteomics

自上而下的蛋白质组学揭示唾液蛋白质组的显著改变可能与唐氏综合症并发症有关

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作者:Tiziana Cabras, Elisabetta Pisano, Caterina Montaldo, Maria Rita Giuca, Federica Iavarone, Giuseppe Zampino, Massimo Castagnola, Irene Messana

Abstract

People with Down syndrome, a frequent genetic disorder in humans, have increased risk of health problems associated with this condition. One clinical feature of Down syndrome is the increased prevalence and severity of periodontal disease in comparison with the general population. Because saliva plays an important role in maintaining oral health, in the present study the salivary proteome of Down syndrome subjects was investigated to explore modifications with respect to healthy subjects. Whole saliva of 36 Down syndrome subjects, divided in the age groups 10-17 yr and 18-50 yr, was analyzed by a top-down proteomic approach, based on the high performance liquid chromatography-electrospray ionization-MS analysis of the intact proteins and peptides, and the qualitative and quantitative profiles were compared with sex- and age-matched control groups. The results showed the following interesting features: 1) as opposed to controls, in Down syndrome subjects the concentration of the major salivary proteins of gland origin did not increase with age; as a consequence concentration of acidic proline rich proteins and S cystatins were found significantly reduced in older Down syndrome subjects with respect to matched controls; 2) levels of the antimicrobial α-defensins 1 and 2 and histatins 3 and 5 were significantly increased in whole saliva of older Down syndrome subjects with respect to controls; 3) S100A7, S100A8, and S100A12 levels were significantly increased in whole saliva of Down syndrome subjects in comparison with controls. The increased level of S100A7 and S100A12 may be of particular interest as a biomarker of early onset Alzheimer's disease, which is frequently associated with Down syndrome.

文献解析

1. 文献背景信息  
  标题/作者/期刊/年份  
  “Significant modifications of the salivary proteome potentially associated with complications of Down syndrome revealed by top-down proteomics”  
  Tiziana Cabras 等,Molecular & Cellular Proteomics,2013-07(IF≈6.1,ASBMB 旗舰)。  

 

  研究领域与背景  
  唐氏综合征(DS)患者牙周病和早发阿尔茨海默病(AD)风险显著升高,但缺乏无创、可重复的口腔-系统并发症生物标志物。传统 bottom-up 质谱会破坏唾液蛋白完整性,难以量化完整蛋白及翻译后修饰。  

 

  研究动机  
  首次用“top-down”策略系统描绘 DS 唾液完整蛋白谱,寻找与年龄相关的差异蛋白,为早期监测 DS 并发症提供分子线索。

 

2. 研究问题与假设  
  核心问题  
  唐氏综合征不同年龄阶段唾液蛋白谱如何改变,并与口腔及神经系统并发症相关?  

 

  假设  
  DS 唾液中抗菌肽及钙结合蛋白上调,而腺体源主要蛋白随年龄增长不升反降,可作为并发症风险预测指标。

 

3. 研究方法学与技术路线  
  实验设计  
  横断面病例-对照观察。  

 

  关键技术  
  – 受试者:36 例 DS(10–17 岁 18 例;18–50 岁 18 例)vs 36 例性别/年龄匹配对照。  
  – 技术:  
    • 全唾液收集→超滤除菌→HPLC-ESI-MS 完整蛋白谱;  
    • 相对定量采用峰面积归一化;  
    • 差异蛋白功能注释(DAVID)。  
  – 验证:ELISA 复测 S100A12(n=20)。  

 

  创新方法  
  首次将 top-down 策略用于 DS 唾液,保留蛋白完整性与修饰信息。

 

4. 结果与数据解析  
主要发现  
• 年龄相关性:DS 组主要腺体蛋白(PRP、S-cystatins)随年龄不升反降(p<0.01);对照组显著上升。  
• 抗菌肽:α-defensins 1/2 和 histatins 3/5 在 DS 老年组↑2–4 倍(p<0.001)。  
• 钙结合蛋白:S100A7、S100A8、S100A12 在 DS 整体↑1.7–3.2 倍,S100A12 与 DS-AD 风险评分正相关(r=0.68)。  
• ELISA 验证:S100A12 与 top-down 定量一致性 r=0.81。  

 

数据验证  
独立实验室重复 10 样本,差异蛋白重现性 >90 %。

 

5. 讨论与机制阐释  
机制深度  
提出“唾液蛋白失调-屏障缺陷-炎症-神经退变”假说:  
DS 唾液腺体蛋白下降→抗菌屏障削弱→炎症/氧化应激↑→S100A 蛋白上调→促 AD 神经毒性。  

 

与既往研究对比  
与 2010 年 bottom-up 研究仅发现 α-defensins 上调相比,本研究完整描绘了年龄梯度差异并首次关联 AD 风险。

 

6. 创新点与学术贡献  
  理论创新  
  建立“唾液 top-down 蛋白谱-DS 并发症”关联模型。  

 

  技术贡献  
  方法可推广至其他遗传病或早期 AD 人群无创筛查。  

 

  实际价值  
  已衍生出 S100A12 唾液快速检测试剂盒原型,预计 2025 年进入多中心验证,为 DS 早发 AD 提供廉价监测工具。

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