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Increase in the density of resting microglia precedes neuritic plaque formation and microglial activation in a transgenic model of Alzheimer's disease

机译:在阿尔茨海默氏病转基因模型中,静息小胶质细胞密度的增加先于神经斑形成和小胶质细胞活化

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The formation of cerebral senile plaques composed of amyloid β peptide (Aβ) is a fundamental feature of Alzheimer's disease (AD). Glial cells and more specifically microglia become reactive in the presence of Aβ. In a triple transgenic model of AD (3 × Tg-AD), we found a significant increase in activated microglia at 12 (by 111%) and 18 (by 88%) months of age when compared with non-transgenic (non-Tg) controls. This microglial activation correlated with Aβ plaque formation, and the activation in microglia was closely associated with Aβ plaques and smaller Aβ deposits. We also found a significant increase in the area density of resting microglia in 3 × Tg-AD animals both at plaque-free stage (at 9 months by 105%) and after the development of A plaques (at 12 months by 54% and at 18 months by 131%). Our results show for the first time that the increase in the density of resting microglia precedes both plaque formation and activation of microglia by extracellular Aβ accumulation. We suggest that AD pathology triggers a complex microglial reaction: at the initial stages of the disease the number of resting microglia increases, as if in preparation for the ensuing activation in an attempt to fight the extracellular Aβ load that is characteristic of the terminal stages of the disease.. ? 2010 Macmillan Publishers Limited
机译:由淀粉样β肽(Aβ)组成的脑老年斑的形成是阿尔茨海默氏病(AD)的基本特征。在存在Aβ的情况下,胶质细胞,更具体地说是小胶质细胞会发生反应。在三重转基因AD(3×Tg-AD)模型中,与非转基因(non-Tg)相比,我们发现在12(分别为111%)和18(88%)个月时激活的小胶质细胞显着增加)控件。这种小胶质细胞活化与Aβ斑块形成有关,而小胶质细胞的活化与Aβ斑块和较小的Aβ沉积物密切相关。我们还发现,在无斑块阶段(9个月时,由105%降低)和A斑块形成之后(12个月时,由54%升高到12个月时),在3×Tg-AD动物中静息小胶质细胞的面积密度显着增加。 18个月,增长131%)。我们的结果首次显示,静息小胶质细胞密度的增加先于噬斑形成和细胞外Aβ积累激活小胶质细胞。我们认为,AD病理会触发复杂的小胶质细胞反应:在疾病的初始阶段,静息的小胶质细胞数量增加,就好像在为随后的活化做准备,以试图对抗细胞终末期特征性的细胞外Aβ负荷一样。这种病.. ? 2010 Macmillan Publishers Limited

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