Department of Laboratory Medicine and Pathobiology, University of Toronto, Canada.
Neurosci Lett. 2011 Mar 29;492(1):5-10. doi: 10.1016/j.neulet.2011.01.035. Epub 2011 Feb 2.
Alzheimer's disease (AD) is a multifactorial disease that results in progressive neurodegeneration. Brain regions are differentially affected in AD. There is also an age-dependent effect on amyloid-beta peptide (Aβ) accumulation and neuroinflammation as disease progresses. In the TgCRND8 APP transgenic mouse model, levels of Aβ species and cytokines were examined as a function of brain region and age. A temporal sequence was observed whereby Aβ accumulation is followed by expression of IL-1β and eventually, of CXCL1, in the hippocampus and olfactory bulb but not the cortex. We have shown for the first time, in an APP mouse model, age and regional differences in Aβ accumulation and cytokine expression.
阿尔茨海默病(AD)是一种多因素疾病,导致进行性神经退行性变。AD 会影响大脑的不同区域。随着疾病的进展,β淀粉样肽(Aβ)的积累和神经炎症也会出现年龄依赖性的影响。在 TgCRND8 APP 转基因小鼠模型中,作为脑区和年龄的函数,检查了 Aβ 物种和细胞因子的水平。观察到一个时间序列,即 Aβ 积累后紧接着是 IL-1β 的表达,最终是 CXCL1 的表达,这在海马体和嗅球中发生,但在皮层中不发生。我们首次在 APP 小鼠模型中显示了 Aβ 积累和细胞因子表达的年龄和区域差异。