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转基因淀粉样蛋白脑疾病模型中胆碱能和单胺能传入纤维的丢失优先发生在淀粉样斑块附近。

Loss of Cholinergic and Monoaminergic Afferents in Transgenic Mouse Model of Cerebral Amyloidosis Preferentially Occurs Near Amyloid Plaques.

机构信息

Department of Neuroscience, University of Minnesota, Minneapolis, MN 55455, USA.

Institute for Translational Neuroscience, University of Minnesota, Minneapolis, MN 55455, USA.

出版信息

Int J Mol Sci. 2024 May 3;25(9):5004. doi: 10.3390/ijms25095004.

DOI:10.3390/ijms25095004
PMID:38732223
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11084680/
Abstract

Alzheimer's disease (AD) is characterized by a loss of neurons in the cortex and subcortical regions. Previously, we showed that the progressive degeneration of subcortical monoaminergic (MAergic) neurons seen in human AD is recapitulated in the (APP/PS) transgenic mouse model. Because degeneration of cholinergic (Ach) neurons is also a prominent feature of AD, we examined the integrity of the Ach system in the APP/PS model. The overall density of Ach fibers is reduced in APP/PS1 mice at 12 and 18 months of age but not at 4 months of age. Analysis of basal forebrain Ach neurons shows no loss of Ach neurons in the APP/PS model. Thus, since MAergic systems show overt cell loss at 18 months of age, the Ach system is less vulnerable to neurodegeneration in the APP/PS1 model. We also examined whether the proximity to Aβ deposition affected the degeneration of Ach and 5-HT afferents. We found that the areas closer to the edges of compact Aβ deposits exhibit a more severe loss of afferents than the areas that are more distal to Aβ deposits. Collectively, the results indicate that the APP/PS model recapitulates the degeneration of multiple subcortical neurotransmitter systems, including the Ach system. In addition, the results indicate that Aβ deposits cause global as well as local toxicity to subcortical afferents.

摘要

阿尔茨海默病(AD)的特征是皮质和皮质下区域神经元的丧失。此前,我们已经证明,在人类 AD 中观察到的皮质下单胺能(MAergic)神经元的进行性退化在 APP/PS 转基因小鼠模型中得到了重现。由于胆碱能(Ach)神经元的退化也是 AD 的一个突出特征,我们研究了 APP/PS 模型中 Ach 系统的完整性。在 12 个月和 18 个月大的 APP/PS1 小鼠中,Ach 纤维的整体密度降低,但在 4 个月大时没有降低。对基底前脑 Ach 神经元的分析显示,APP/PS 模型中没有 Ach 神经元的丢失。因此,由于 MAergic 系统在 18 个月时表现出明显的细胞丢失,因此 Ach 系统在 APP/PS1 模型中对神经退行性变的敏感性较低。我们还研究了 Ach 和 5-HT 传入纤维的退化是否接近 Aβ沉积的影响。我们发现,靠近致密 Aβ沉积物边缘的区域比距离 Aβ沉积物更远的区域表现出更严重的传入纤维丢失。总之,这些结果表明,APP/PS 模型重现了包括 Ach 系统在内的多个皮质下神经递质系统的退化。此外,这些结果表明,Aβ 沉积对皮质下传入纤维造成了全局和局部毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/a9ab95adbee6/ijms-25-05004-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/8dbf04d6a158/ijms-25-05004-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/7f408f61225e/ijms-25-05004-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/870e431dc2b3/ijms-25-05004-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/5ef0e3c1e1ee/ijms-25-05004-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/a9ab95adbee6/ijms-25-05004-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/8dbf04d6a158/ijms-25-05004-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/7f408f61225e/ijms-25-05004-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/870e431dc2b3/ijms-25-05004-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/5ef0e3c1e1ee/ijms-25-05004-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf62/11084680/a9ab95adbee6/ijms-25-05004-g005.jpg

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