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Directed conversion of Alzheimer's disease patient skin fibroblasts into functional neurons

机译:阿尔茨海默氏病患者皮肤成纤维细胞定向转化为功能神经元

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Directed conversion of mature human cells, as from fibroblasts to neurons, is of potential clinical utility for neurological disease modeling as well as cell therapeutics. Here, we describe the efficient generation of human-induced neuronal (hiN) cells from adult skin fibroblasts of unaffected individuals and Alzheimer's patients, using virally transduced transcription regulators and extrinsic support factors. hiN cells from unaffected individuals display morphological, electrophysiological, and gene expression profiles that typify glutamatergic forebrain neurons and are competent to integrate functionally into the rodent CNS. hiN cells from familial Alzheimer disease (FAD) patients with presenilin-1 or -2 mutations exhibit altered processing and localization of amyloid precursor protein (APP) and increased production of Aβ, relative to the source patient fibroblasts or hiN cells from unaffected individuals. Together, our findings demonstrate directed conversion of human fibroblasts to a neuronal phenotype and reveal cell type-selective pathology in hiN cells derived from FAD patients.
机译:从成纤维细胞到神经元的成熟人类细胞的定向转化对于神经疾病建模以及细胞治疗具有潜在的临床实用性。在这里,我们描述了使用病毒转导的转录调节因子和外源性支持因子,从未受影响的个体和阿尔茨海默氏病患者的成年皮肤成纤维细胞中高效生成人诱导的神经元(hiN)细胞。来自未受影响个体的hiN细胞显示出代表谷氨酸能前脑神经元的形态,电生理和基因表达谱,并且能够将其功能整合到啮齿动物中枢神经系统中。相对于未患病个体的源患者成纤维细胞或hiN细胞,来自早老素-1或-2突变的家族性阿尔茨海默病(FAD)患者的hiN细胞显示出淀粉样前体蛋白(APP)的加工和定位改变,Aβ产生增加。在一起,我们的发现表明人类成纤维细胞定向转化为神经元表型,并揭示了源自FAD患者的hiN细胞的细胞类型选择性病理。

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