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利用扩增和纯化的干细胞衍生培养物确定人类运动神经元的神经营养需求。

Neurotrophic requirements of human motor neurons defined using amplified and purified stem cell-derived cultures.

作者信息

Lamas Nuno Jorge, Johnson-Kerner Bethany, Roybon Laurent, Kim Yoon A, Garcia-Diaz Alejandro, Wichterle Hynek, Henderson Christopher E

机构信息

Project A.L.S./Jenifer Estess Laboratory for Stem Cell Research, New York, New York, United States of America; Center for Motor Neuron Biology and Disease, Columbia University Medical Center, New York, New York, United States of America; Department of Rehabilitation and Regenerative Medicine, Columbia University Medical Center, New York, New York, United States of America; Department of Pathology and Cell Biology, Columbia University Medical Center, New York, New York, United States of America; Department of Neurology, Columbia University Medical Center, New York, New York, United States of America; Department of Neuroscience, Columbia University Medical Center, New York, New York, United States of America; Columbia Stem Cell Initiative, Columbia University Medical Center, New York, New York, United States of America; Columbia Translational Neuroscience Initiative, Columbia University Medical Center, New York, New York, United States of America; Life and Health Sciences Research Institute, School of Health Sciences, University of Minho, Braga, Minho, Portugal; ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Minho, Portugal.

Project A.L.S./Jenifer Estess Laboratory for Stem Cell Research, New York, New York, United States of America; Center for Motor Neuron Biology and Disease, Columbia University Medical Center, New York, New York, United States of America; Department of Rehabilitation and Regenerative Medicine, Columbia University Medical Center, New York, New York, United States of America; Department of Pathology and Cell Biology, Columbia University Medical Center, New York, New York, United States of America; Department of Neurology, Columbia University Medical Center, New York, New York, United States of America; Department of Neuroscience, Columbia University Medical Center, New York, New York, United States of America; Columbia Stem Cell Initiative, Columbia University Medical Center, New York, New York, United States of America; Columbia Translational Neuroscience Initiative, Columbia University Medical Center, New York, New York, United States of America.

出版信息

PLoS One. 2014 Oct 22;9(10):e110324. doi: 10.1371/journal.pone.0110324. eCollection 2014.

Abstract

Human motor neurons derived from embryonic and induced pluripotent stem cells (hESCs and hiPSCs) are a potentially important tool for studying motor neuron survival and pathological cell death. However, their basic survival requirements remain poorly characterized. Here, we sought to optimize a robust survival assay and characterize their response to different neurotrophic factors. First, to increase motor neuron yield, we screened a small-molecule collection and found that the Rho-associated kinase (ROCK) inhibitor Y-27632 enhances motor neuron progenitor proliferation up to 4-fold in hESC and hiPSC cultures. Next, we FACS-purified motor neurons expressing the Hb9::GFP reporter from Y-27632-amplified embryoid bodies and cultured them in the presence of mitotic inhibitors to eliminate dividing progenitors. Survival of these purified motor neurons in the absence of any other cell type was strongly dependent on neurotrophic support. GDNF, BDNF and CNTF all showed potent survival effects (EC(50) 1-2 pM). The number of surviving motor neurons was further enhanced in the presence of forskolin and IBMX, agents that increase endogenous cAMP levels. As a demonstration of the ability of the assay to detect novel neurotrophic agents, Y-27632 itself was found to support human motor neuron survival. Thus, purified human stem cell-derived motor neurons show survival requirements similar to those of primary rodent motor neurons and can be used for rigorous cell-based screening.

摘要

源自胚胎干细胞和诱导多能干细胞(hESC和hiPSC)的人类运动神经元是研究运动神经元存活和病理性细胞死亡的潜在重要工具。然而,它们基本的存活需求仍未得到充分表征。在此,我们试图优化一种可靠的存活检测方法,并表征它们对不同神经营养因子的反应。首先,为了提高运动神经元产量,我们筛选了一个小分子化合物库,发现Rho相关激酶(ROCK)抑制剂Y-27632可使hESC和hiPSC培养物中的运动神经元祖细胞增殖提高至4倍。接下来,我们通过荧光激活细胞分选(FACS)从Y-27632扩增的胚状体中纯化出表达Hb9::GFP报告基因的运动神经元,并在有丝分裂抑制剂存在的情况下进行培养,以消除正在分裂的祖细胞。在没有任何其他细胞类型的情况下,这些纯化的运动神经元的存活强烈依赖于神经营养支持。胶质细胞源性神经营养因子(GDNF)、脑源性神经营养因子(BDNF)和睫状神经营养因子(CNTF)均显示出强大的存活效应(半数有效浓度(EC(50))为1-2 pM)。在存在可提高内源性环磷酸腺苷(cAMP)水平的福斯高林和异丁基甲基黄嘌呤(IBMX)的情况下,存活的运动神经元数量进一步增加。作为该检测方法检测新型神经营养因子能力的一个例证,发现Y-27632本身可支持人类运动神经元存活。因此,纯化的人类干细胞源性运动神经元显示出与原代啮齿动物运动神经元相似的存活需求,可用于严格的基于细胞的筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118c/4206291/a0a10647ac08/pone.0110324.g001.jpg

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