4.8 Article

REST and Neural Gene Network Dysregulation in iPSC Models of Alzheimer's Disease

期刊

CELL REPORTS
卷 26, 期 5, 页码 1112-+

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2019.01.023

关键词

-

资金

  1. NIH [DP1OD006849, R01AG046174, RF1AG048056, RF1AG048029, RM1HG008525]
  2. Paul F. Glenn Foundation for Medical Research
  3. Fidelity Biosciences Research Initiative
  4. Robert A. and Renee E. Belfer Family Foundation
  5. Cure Alzheimer's Fund
  6. DFG [ME 4810/1-1]
  7. IBRO/ISN Research Fellowship

向作者/读者索取更多资源

The molecular basis of the earliest neuronal changes that lead to Alzheimer's disease (AD) is unclear. Here, we analyze neural cells derived from sporadic AD (SAD), APOE4 gene-edited and control induced pluripotent stem cells (iPSCs). We observe major differences in iPSC-derived neural progenitor (NP) cells and neurons in gene networks related to neuronal differentiation, neurogenesis, and synaptic transmission. The iPSC-derived neural cells from SAD patients exhibit accelerated neural differentiation and reduced progenitor cell renewal. Moreover, a similar phenotype appears in NP cells and cerebral organoids derived from APOE4 iPSCs. Impaired function of the transcriptional repressor REST is strongly implicated in the altered transcriptome and differentiation state. SAD and APOE4 expression result in reduced REST nuclear translocation and chromatin binding, and disruption of the nuclear lamina. Thus, dysregulation of neural gene networks may set in motion the pathologic cascade that leads to AD.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据