{"title":"Glymphatic Efficiency Is a Critical Factor for Using Abnormal Tau in Peripheral Tissues as Biomarker for Alzheimer's Disease.","authors":"Yahuan Lou, Colin Carlock, Jean Wu","doi":"10.29011/2576-9588.100030","DOIUrl":null,"url":null,"abstract":"<p><p>Alzheimer's Disease or other dementias are characterized by the accumulation of abnormal tau and amyloid β peptides in brains. Therefore, abnormal tau and amyloid peptides in peripheral tissues or blood have been explored as diagnostic biomarkers. On the other hand, recent studies have revealed glymphatics a special drainage system for brain's wastes. We aimed to investigate whether effectiveness of glymphatic system affects the quantity of abnormal tau in the peripheral tissues. We have previously shown that aged IL33 KO (<i>Il33</i> <sup>-/-</sup>) mice develop Alzheimer's like disease. Despite a large quantity of abnormal tau in brains, <i>Il33</i> <sup>-/-</sup> mice showed a much lower amount of abnormal tau drained to the peripheral tissues kidneys than in wild type mice. Our further study showed that it was caused by defective glymphatic drainage since Il33 KO impaired glymphatics. Thus, it is necessary to identify biomarkers, which can evaluate efficiency of glymphatic drainage. Simultaneous measurement of these biomarkers and abnormal tau in peripheral tissues or blood may be critical for accurate diagnosis of Alzheimer's disease.</p>","PeriodicalId":93081,"journal":{"name":"Biomarkers and applications","volume":"2018 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729990/pdf/nihms-1043241.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomarkers and applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29011/2576-9588.100030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2018/12/28 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Alzheimer's Disease or other dementias are characterized by the accumulation of abnormal tau and amyloid β peptides in brains. Therefore, abnormal tau and amyloid peptides in peripheral tissues or blood have been explored as diagnostic biomarkers. On the other hand, recent studies have revealed glymphatics a special drainage system for brain's wastes. We aimed to investigate whether effectiveness of glymphatic system affects the quantity of abnormal tau in the peripheral tissues. We have previously shown that aged IL33 KO (Il33-/-) mice develop Alzheimer's like disease. Despite a large quantity of abnormal tau in brains, Il33-/- mice showed a much lower amount of abnormal tau drained to the peripheral tissues kidneys than in wild type mice. Our further study showed that it was caused by defective glymphatic drainage since Il33 KO impaired glymphatics. Thus, it is necessary to identify biomarkers, which can evaluate efficiency of glymphatic drainage. Simultaneous measurement of these biomarkers and abnormal tau in peripheral tissues or blood may be critical for accurate diagnosis of Alzheimer's disease.
阿尔茨海默病或其他痴呆症的特征是大脑中积累异常的 tau 和淀粉样 β 肽。因此,外周组织或血液中的异常 tau 和淀粉样肽已被探索用作诊断生物标志物。另一方面,最近的研究发现甘油三酯是大脑废物的特殊排泄系统。我们的目的是研究甘油系统的有效性是否会影响外周组织中异常 tau 的数量。我们曾研究发现,IL33 KO(Il33 -/-)小鼠在老化后会患上类似阿尔茨海默病的疾病。尽管大脑中存在大量的异常tau,但Il33 -/-小鼠外周组织肾脏中的异常tau却比野生型小鼠少得多。我们的进一步研究表明,这是由于Il33 KO损害了甘油三酯,导致甘油三酯排泄功能缺陷所致。因此,有必要确定能评估甘液引流效率的生物标志物。同时测量这些生物标志物和外周组织或血液中的异常 tau 可能是准确诊断阿尔茨海默病的关键。