Laboratory of Molecular Neurobiology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.
Biomaterials. 2014 Feb;35(5):1420-8. doi: 10.1016/j.biomaterials.2013.11.028. Epub 2013 Nov 27.
The recent progress in stem cell techniques has broadened the horizon for in vitro disease modeling. For desired in vivo like phenotypes, not only correct cell type specification will be critical, the microenvironmental context will be essential to achieve relevant responses. We demonstrate how a three dimensional (3D) culture of stem cell derived neurons can induce in vivo like responses related to Alzheimer's disease, not recapitulated with conventional 2D cultures. To acquire a neural population of cells we differentiated neurons from neuroepithelial stem cells, derived from induced pluripotent stem cells. p21-activated kinase mediated sensing of Aβ oligomers was only possible in the 3D environment. Further, the 3D phenotype showed clear effects on F-actin associated proteins, connected to the disease processes. We propose that the 3D in vitro model has higher resemblance to the AD pathology than conventional 2D cultures and could be used in further studies of the disease.
最近干细胞技术的进展拓宽了体外疾病建模的视野。为了获得所需的类似体内的表型,不仅正确的细胞类型特化将是关键,微环境背景对于实现相关反应也将是至关重要的。我们展示了如何通过三维(3D)培养干细胞衍生的神经元来诱导与阿尔茨海默病相关的类似体内的反应,这是传统的 2D 培养无法重现的。为了获得神经细胞群体,我们从诱导多能干细胞中分化出神经上皮干细胞来源的神经元。只有在 3D 环境中才能检测到 p21 激活激酶介导的 Aβ 寡聚物感应。此外,3D 表型对与疾病过程相关的 F-肌动蛋白相关蛋白显示出明显的影响。我们提出,与传统的 2D 培养相比,3D 体外模型与 AD 病理学更相似,可用于进一步研究该疾病。