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Establishing Cerebral Organoids as Models of Human-Specific Brain Evolution

机译:建立脑细胞器作为人体特异性脑进化模型

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Direct comparisons of human and non-human primate brains can reveal molecular pathways underlying remarkable specializations of the human brain. However, chimpanzee tissue is inaccessible during neocortical neurogenesis when differences in brain size first appear. To identify human-specific features of cortical development, we leveraged recent innovations that permit generating pluripotent stem cell-derived cerebral organoids from chimpanzee. Despite metabolic differences, organoid models preserve gene regulatory networks related to primary cell types and developmental processes. We further identified 261 differentially expressed genes in human compared to both chimpanzee organoids and macaque cortex, enriched for recent gene duplications, and including multiple regulators of P13K-AKT-mTOR signaling. We observed increased activation of this pathway in human radial glia, dependent on two receptors upregulated specifically in human: INSR and ITGB8. Our findings establish a platform for systematic analysis of molecular changes contributing to human brain development and evolution.
机译:人类和非人灵长类动物大脑的直接比较可以揭示人类脑的显着专业的分子途径。然而,当首次出现脑大小的差异时,在新生科学神经发生期间,黑猩猩组织无法进入。为了识别皮质发育的人类特异性,我们利用最近的创新,允许从黑猩猩产生多能干细胞衍生的脑细胞素。尽管代谢差异,但有机体模型保留了与原发性细胞类型和发育过程相关的基因调节网络。我们进一步确定了与黑猩猩有机体和猕猴皮质的261种差异表达的基因,富集为最近的基因重复,包括P13K-AKT-MTOR信号传导的多个调节器。我们观察到人类径向胶质峡在人径向胶质型途径的增加,依赖于在人类:INSR和ITGB8中特异性上调的两种受体。我们的调查结果建立了对人脑发展和进化有助于促进分子变化的系统分析平台。

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