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人 LUHMES 和 NES 细胞作为研究神经元中的初级纤毛的模型。

Human LUHMES and NES cells as models for studying primary cilia in neurons.

机构信息

Karolinska Institute, Department of Biosciences and Nutrition, Huddinge, Sweden.

Karolinska Institute, Department of Women's and Children's Health and Center for Psychiatry Research, Center of Neurodevelopmental Disorders (KIND), Division of Neuropsychiatry, Stockholm, Sweden; Astrid Lindgren Children's Hospital, Karolinska University Hospital, Region Stockholm, Stockholm, Sweden.

出版信息

Methods Cell Biol. 2023;176:27-41. doi: 10.1016/bs.mcb.2022.12.012. Epub 2023 Jan 28.

Abstract

Primary cilia are antenna-like organelles emanating from the cell surface. They are involved in cell-to-cell communication and bidirectional signal transduction to/from the extracellular environment. During brain formation, cilia critically aid in neurogenesis and maturation of neuronal structures such as axons, dendrites and synapses. Aberrations in cilia function can induce neuron differentiation defects and pathological consequences of varying severity, resulting in ciliopathies and likely a number of neurodevelopmental disorders. Despite the documented relevance of cilia for proper brain development, human neuronal models to recognize and study cilia biology are still scarce. We have established two types of cell models, Lund Human Mesencephalic (LUHMES) cells and neuroepithelial stem (NES) cells derived from induced pluripotent stem cells (iPSC), to investigate cilia biology in both proliferating neuronal progenitors/precursors and during the entire neuron differentiation and maturation process. We employ improved immunocytochemistry assays able to specifically detect cilia by confocal and super-resolution microscopy. We provide straightforward and robust methods to easily maintain cells in culture, for immunostaining and characterization of cilia orientation, anatomy and shape in human neurons across all stages of differentiation.

摘要

初级纤毛是从细胞表面伸出的类似天线的细胞器。它们参与细胞间的通讯和双向信号转导,将信号从细胞外环境传递到细胞内,或从细胞内传递到细胞外。在大脑形成过程中,纤毛对神经发生和神经元结构(如轴突、树突和突触)的成熟至关重要。纤毛功能异常会导致神经元分化缺陷和不同严重程度的病理后果,从而引发纤毛病,并可能导致许多神经发育障碍。尽管纤毛对大脑正常发育的重要性已得到证实,但用于识别和研究纤毛生物学的人类神经元模型仍然很少。我们建立了两种细胞模型,即 Lund Human Mesencephalic (LUHMES) 细胞和神经上皮干细胞 (NES) 细胞,这些细胞源自诱导多能干细胞 (iPSC),以研究增殖性神经元祖细胞/前体细胞以及整个神经元分化和成熟过程中的纤毛生物学。我们采用了改进的免疫细胞化学检测方法,能够通过共聚焦和超分辨率显微镜特异性检测纤毛。我们提供了简单而稳健的方法,可轻松地在培养物中维持细胞,用于免疫染色和表征分化过程中各个阶段的人类神经元的纤毛取向、结构和形状。

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