Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Department of Health Sciences Research, Mayo Clinic, Jacksonville, FL, USA.
Nat Commun. 2021 Apr 19;12(1):2311. doi: 10.1038/s41467-021-22399-3.
Selective vulnerability of different brain regions is seen in many neurodegenerative disorders. The hippocampus and cortex are selectively vulnerable in Alzheimer's disease (AD), however the degree of involvement of the different brain regions differs among patients. We classified corticolimbic patterns of neurofibrillary tangles in postmortem tissue to capture extreme and representative phenotypes. We combined bulk RNA sequencing with digital pathology to examine hippocampal vulnerability in AD. We identified hippocampal gene expression changes associated with hippocampal vulnerability and used machine learning to identify genes that were associated with AD neuropathology, including SERPINA5, RYBP, SLC38A2, FEM1B, and PYDC1. Further histologic and biochemical analyses suggested SERPINA5 expression is associated with tau expression in the brain. Our study highlights the importance of embracing heterogeneity of the human brain in disease to identify disease-relevant gene expression.
在许多神经退行性疾病中,不同的大脑区域存在选择性易损性。在阿尔茨海默病(AD)中,海马体和皮质是选择性易损的,但不同患者的不同大脑区域的受累程度不同。我们对死后组织中的神经纤维缠结进行皮质边缘模式分类,以捕获极端和代表性的表型。我们将批量 RNA 测序与数字病理学相结合,研究 AD 中的海马体易损性。我们确定了与海马体易损性相关的海马体基因表达变化,并使用机器学习来识别与 AD 神经病理学相关的基因,包括 SERPINA5、RYBP、SLC38A2、FEM1B 和 PYDC1。进一步的组织学和生化分析表明,SERPINA5 的表达与大脑中的 tau 表达有关。我们的研究强调了在疾病中接受人脑异质性的重要性,以确定与疾病相关的基因表达。