Queensland Institute of Medical Research, Brisbane, Queensland 4006, Australia.
Hum Mol Genet. 2013 Jun 15;22(12):2495-509. doi: 10.1093/hmg/ddt101. Epub 2013 Mar 7.
The autosomal recessive disorder ataxia-telangiectasia (A-T) is characterized by genome instability, cancer predisposition and neurodegeneration. Although the role of ataxia-telangiectasia mutated (ATM) protein, the protein defective in this syndrome, is well described in the response to DNA damage, its role in protecting the nervous system is less clear. We describe the establishment and characterization of patient-specific stem cells that have the potential to address this shortcoming. Olfactory neurosphere (ONS)-derived cells were generated from A-T patients, which expressed stem cell markers and exhibited A-T molecular and cellular characteristics that included hypersensitivity to radiation, defective radiation-induced signaling and cell cycle checkpoint defects. Introduction of full-length ATM cDNA into these cells corrected defects in the A-T cellular phenotype. Gene expression profiling and pathway analysis revealed defects in multiple cell signaling pathways associated with ATM function, with cell cycle, cell death and DNA damage response pathways being the most significantly dysregulated. A-T ONS cells were also capable of differentiating into neural progenitors, but they were defective in neurite formation, number of neurites and length of these neurites. Thus, ONS cells are a patient-derived neural stem cell model that recapitulate the phenotype of A-T, do not require genetic reprogramming, have the capacity to differentiate into neurons and have potential to delineate the neurological defect in these patients.
常染色体隐性遗传疾病共济失调毛细血管扩张症(A-T)的特征是基因组不稳定、易患癌症和神经退行性变。尽管这种综合征中缺陷的蛋白 ATM(ataxia-telangiectasia mutated)蛋白在应对 DNA 损伤中的作用已有详细描述,但它在保护神经系统方面的作用尚不清楚。我们描述了建立和表征具有潜在解决这一不足的患者特异性干细胞的方法。从 A-T 患者中生成了嗅球神经球(ONS)衍生细胞,这些细胞表达干细胞标记物,并表现出 A-T 的分子和细胞特征,包括对辐射的超敏感性、辐射诱导信号的缺陷以及细胞周期检查点缺陷。将全长 ATM cDNA 引入这些细胞中可纠正 A-T 细胞表型缺陷。基因表达谱和途径分析显示,与 ATM 功能相关的多个细胞信号通路存在缺陷,细胞周期、细胞死亡和 DNA 损伤反应途径的失调最为显著。A-T ONS 细胞也能够分化为神经祖细胞,但它们在神经突形成、神经突数量和这些神经突的长度方面存在缺陷。因此,ONS 细胞是一种患者来源的神经干细胞模型,可再现 A-T 的表型,不需要遗传重编程,具有分化为神经元的能力,并有可能阐明这些患者的神经缺陷。