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淀粉样斑块形成先于树突棘缺失。

Amyloid plaque formation precedes dendritic spine loss.

机构信息

Center for Neuropathology, Ludwig-Maximilians University, Munich, Germany.

出版信息

Acta Neuropathol. 2012 Dec;124(6):797-807. doi: 10.1007/s00401-012-1047-8. Epub 2012 Sep 21.

DOI:10.1007/s00401-012-1047-8
PMID:22993126
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3508278/
Abstract

Amyloid-beta plaque deposition represents a major neuropathological hallmark of Alzheimer's disease. While numerous studies have described dendritic spine loss in proximity to plaques, much less is known about the kinetics of these processes. In particular, the question as to whether synapse loss precedes or follows plaque formation remains unanswered. To address this question, and to learn more about the underlying kinetics, we simultaneously imaged amyloid plaque deposition and dendritic spine loss by applying two-photon in vivo microscopy through a cranial window in double transgenic APPPS1 mice. As a result, we first observed that the rate of dendritic spine loss in proximity to plaques is the same in both young and aged animals. However, plaque size only increased significantly in the young cohort, indicating that spine loss persists even many months after initial plaque appearance. Tracking the fate of individual spines revealed that net spine loss is caused by increased spine elimination, with the rate of spine formation remaining constant. Imaging of dendritic spines before and during plaque formation demonstrated that spine loss around plaques commences at least 4 weeks after initial plaque formation. In conclusion, spine loss occurs, shortly but with a significant time delay, after the birth of new plaques, and persists in the vicinity of amyloid plaques over many months. These findings hence give further hope to the possibility that there is a therapeutic window between initial amyloid plaque deposition and the onset of structural damage at spines.

摘要

淀粉样β斑块沉积是阿尔茨海默病的主要神经病理学特征之一。虽然有许多研究描述了斑块附近树突棘的丢失,但这些过程的动力学却知之甚少。特别是,突触丢失是先于斑块形成还是后于斑块形成的问题仍然没有答案。为了解决这个问题,并更多地了解潜在的动力学,我们通过在双转基因 APPPS1 小鼠的颅窗中应用双光子活体显微镜,同时对淀粉样斑块沉积和树突棘丢失进行成像。结果,我们首先观察到,斑块附近树突棘丢失的速度在年轻和年老动物中是相同的。然而,斑块大小仅在年轻组中显著增加,这表明即使在最初出现斑块后的数月内,棘突丢失仍在持续。跟踪单个棘突的命运表明,净棘突丢失是由棘突消除增加引起的,而棘突形成的速度保持不变。在斑块形成前后对树突棘的成像表明,斑块周围的棘突丢失至少在最初斑块形成后 4 周开始。总之,在新斑块形成后不久,即发生了棘突丢失,而且在数月的时间里,这种丢失在淀粉样斑块附近持续存在。这些发现进一步表明,在初始淀粉样斑块沉积和棘突结构损伤开始之间存在治疗窗口的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/ff644e94a2f4/401_2012_1047_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/f54182ffc6d5/401_2012_1047_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/b6c60f5e66df/401_2012_1047_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/d4dc12a4e0bb/401_2012_1047_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/535d834088a8/401_2012_1047_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/ca8b391474be/401_2012_1047_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/ff644e94a2f4/401_2012_1047_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/f54182ffc6d5/401_2012_1047_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/b6c60f5e66df/401_2012_1047_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/d4dc12a4e0bb/401_2012_1047_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/535d834088a8/401_2012_1047_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/ca8b391474be/401_2012_1047_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/800f/3508278/ff644e94a2f4/401_2012_1047_Fig6_HTML.jpg

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