首页> 美国卫生研究院文献>NPJ Schizophrenia >Schizophrenia patient-derived olfactory neurosphere-derived cells do not respond to extracellular reelin
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Schizophrenia patient-derived olfactory neurosphere-derived cells do not respond to extracellular reelin

机译:精神分裂症患者来源的嗅觉神经球来源的细胞对细胞外瑞林没有反应

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摘要

Reelin expression is reduced in various regions in the post-mortem brain of schizophrenia patients but the exact role of reelin function in the neurobiology of schizophrenia remains elusive. Absence of reelin in knockout mouse causes inverted lamination of the neocortex due to aberrant neuronal migration. The aim of this study was to utilize patient-derived olfactory neurosphere-derived (ONS) cells to investigate whether extracellular reelin alters cell motility in schizophrenia patient-derived cells. ONS cells from nine patients were compared with cells from nine matched healthy controls. Automated high-throughput imaging and analysis were used to track motility of individual living cells on reelin-coated surfaces produced from reelin secreted into the medium by HEK293FT cells transfected with the full-length reelin plasmid pCrl. Automated assays were used to quantify intracellular cytoskeleton composition, cell morphology, and focal adhesions. Expression of reelin and components of the reelin signaling pathway were measured by western blot and flow cytometry. Reelin inhibited the motility of control cells but not patient cells, and increased the number and size of focal adhesions in control cells but not patient cells. Patient and control cells expressed similar levels of the reelin receptors and the reelin signaling protein, Dab1, but patient cells expressed less reelin. Patient cells were smaller than control cells and had less actin and acetylated α-tubulin, components of the cytoskeleton. These findings are the first direct evidence that cellular responses to reelin are impaired in schizophrenia and are consistent with the role of reelin in cytoarchitectural deficits observed in schizophrenia patient brains.
机译:在精神分裂症患者的死后大脑的各个区域中,Reelin表达降低,但是reelin功能在精神分裂症的神经生物学中的确切作用仍然难以捉摸。由于异常的神经元迁移,基因敲除小鼠中缺少reelin会导致新皮层的倒层。这项研究的目的是利用患者来源的嗅觉神经球来源(ONS)细胞来研究细胞外瑞林是否会改变精神分裂症患者来源细胞的细胞运动性。将来自9位患者的ONS细胞与来自9位匹配的健康对照的细胞进行了比较。自动化的高通量成像和分析用于追踪由全长reelin质粒pCrl转染的HEK293FT细胞分泌的reelin分泌的reelin涂层表面上的单个活细胞的运动。自动化分析用于定量细胞内细胞骨架组成,细胞形态和粘着斑。 reelin的表达和reelin信号通路的组成部分通过Western印迹和流式细胞仪测量。 Reelin抑制对照细胞而非患者细胞的运动,并增加了对照细胞而非患者细胞中粘着斑的数量和大小。患者和对照细胞表达的reelin受体和reelin信号蛋白Dab1水平相似,但患者细胞表达的reelin较少。患者细胞比对照细胞小,肌动蛋白和乙酰化的α-微管蛋白(细胞骨架的组成部分)少。这些发现是精神分裂症中对瑞林的细胞反应受损的第一个直接证据,并且与瑞林在精神分裂症患者大脑中观察到的细胞结构缺陷中的作用一致。

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