分析 iPSC 衍生的 21 三体综合征神经祖细胞的基因型效应和个体间差异。

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sarah E Lee, Laura L Baxter, Monica I Duran, Samuel D Morris, Iman A Mosley, Kevin A Fuentes, Jeroen L A Pennings, Faycal Guedj, Diana W Bianchi
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引用次数: 0

摘要

人类 21 号染色体三体(T21)导致唐氏综合征(DS),这是一种最常见的活产常染色体非整倍体。T21 会引发全基因组转录组的改变,从而导致唐氏综合征患者出现多种非典型表型,这些表型的穿透力和表现力差异很大。其中许多表型,包括非典型神经发育,都是在产前出现的。为了体外分析导致与 T21 相关的神经系统改变的细胞和分子机制,我们创建并鉴定了一组基因组多样化的 T21 和超常诱导多能干细胞(iPSCs)。随后,我们分化了这些 iPSCs,生成了一组神经祖细胞(NPCs)。在描述T21基因型效应的同时,我们还发现T21 NPCs在生长速度、氧化应激、衰老特征以及基因和蛋白质表达方面表现出个体间差异。T21 NPC 的通路富集分析确定了囊泡运输、DNA 修复和细胞对应激反应的通路。这些结果表明了细胞水平上与 T21 相关的变异性,并提示我们不应仅将 DS 患者的细胞系作为同质群体进行分析。对大量不同基因的样本进行研究可能会更全面地揭示非整倍体对T21细胞类型的转录组和表型特征的影响。我们创建了一组基因组不同的T21和非整倍体诱导多能干细胞(iPSCs),随后将其分化为神经祖细胞(NPCs)。T21 NPCs表现出生长减弱、氧化应激增加以及基因和蛋白质表达的个体间差异性。这种个体间变异性表明,通过对大量不同基因的 T21 样本进行研究,可以更全面地揭示非整倍体的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of genotype effects and inter-individual variability in iPSC-derived trisomy 21 neural progenitor cells.

Trisomy of human chromosome 21 (T21) gives rise to Down syndrome (DS), the most frequent live-born autosomal aneuploidy. T21 triggers genome-wide transcriptomic alterations that result in multiple atypical phenotypes with highly variable penetrance and expressivity in individuals with DS. Many of these phenotypes, including atypical neurodevelopment, emerge prenatally. To enable in vitro analyses of the cellular and molecular mechanisms leading to the neurological alterations associated with T21, we created and characterized a panel of genomically diverse T21 and euploid induced pluripotent stem cells (iPSCs). We subsequently differentiated these iPSCs to generate a panel of neural progenitor cells (NPCs). Alongside characterizing genotype effects from T21, we found that T21 NPCs showed inter-individual variability in growth rates, oxidative stress, senescence characteristics, and gene and protein expression. Pathway enrichment analyses of T21 NPCs identified vesicular transport, DNA repair, and cellular response to stress pathways. These results demonstrate T21-associated variability at the cellular level and suggest that cell lines from individuals with DS should not solely be analyzed as a homogenous population. Examining large cohorts of genetically diverse samples may more fully reveal the effects of aneuploidy on transcriptomic and phenotypic characteristics in T21 cell types. A panel of genomically diverse T21 and euploid induced pluripotent stem cells (iPSCs) were created and subsequently differentiated into neural progenitor cells (NPCs). T21 NPCs showed reduced growth, increased oxidative stress, and inter-individual variability in gene and protein expression. This inter-individual variability suggests that studies with large cohorts of genetically diverse T21 samples may more fully reveal the effects of aneuploidy.

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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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