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LIF 信号在人皮质发育过程中调节外放射状胶质向中间神经元的命运。

LIF signaling regulates outer radial glial to interneuron fate during human cortical development.

机构信息

Department of Neurology, University of California, San Francisco (UCSF), San Francisco, CA 94143, USA; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, UCSF, San Francisco, CA 94143, USA; School of Biological and Health Systems Engineering, Arizona State University (ASU), Tempe, AZ 85281, USA.

Department of Neurology, University of California, San Francisco (UCSF), San Francisco, CA 94143, USA; The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, UCSF, San Francisco, CA 94143, USA.

出版信息

Cell Stem Cell. 2023 Oct 5;30(10):1382-1391.e5. doi: 10.1016/j.stem.2023.08.009. Epub 2023 Sep 5.

Abstract

Radial glial (RG) development is essential for cerebral cortex growth and organization. In humans, the outer radial glia (oRG) subtype is expanded and gives rise to diverse neurons and glia. However, the mechanisms regulating oRG differentiation are unclear. oRG cells express leukemia-inhibitory factor (LIF) receptors during neurogenesis, and consistent with a role in stem cell self-renewal, LIF perturbation impacts oRG proliferation in cortical tissue and organoids. Surprisingly, LIF treatment also increases the production of inhibitory interneurons (INs) in cortical cultures. Comparative transcriptomic analysis identifies that the enhanced IN population resembles INs produced in the caudal ganglionic eminence. To evaluate whether INs could arise from oRGs, we isolated primary oRG cells and cultured them with LIF. We observed the production of INs from oRG cells and an increase in IN abundance following LIF treatment. Our observations suggest that LIF signaling regulates the capacity of oRG cells to generate INs.

摘要

放射状胶质(RG)的发育对于大脑皮层的生长和组织至关重要。在人类中,外放射状胶质(oRG)亚型被扩展,并产生各种神经元和神经胶质。然而,调节 oRG 分化的机制尚不清楚。oRG 细胞在神经发生过程中表达白血病抑制因子(LIF)受体,与干细胞自我更新的作用一致,LIF 干扰会影响皮质组织和类器官中的 oRG 增殖。令人惊讶的是,LIF 处理还会增加皮质培养物中抑制性中间神经元(IN)的产生。比较转录组分析表明,增强的 IN 群体类似于尾状神经节隆起中产生的 IN。为了评估 IN 是否可以从 oRG 产生,我们分离了原代 oRG 细胞并在 LIF 存在下培养它们。我们观察到 oRG 细胞产生 IN,并且 LIF 处理后 IN 丰度增加。我们的观察表明,LIF 信号调节 oRG 细胞产生 IN 的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef12/10591955/67ed0a8f5f34/nihms-1929468-f0001.jpg

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