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源自人类多能干细胞的多能尾神经祖细胞,可分化为中枢和外周神经系统谱系。

Multipotent caudal neural progenitors derived from human pluripotent stem cells that give rise to lineages of the central and peripheral nervous system.

作者信息

Denham Mark, Hasegawa Kouichi, Menheniott Trevelyan, Rollo Ben, Zhang Dongcheng, Hough Shelley, Alshawaf Abdullah, Febbraro Fabia, Ighaniyan Samiramis, Leung Jessie, Elliott David A, Newgreen Donald F, Pera Martin F, Dottori Mirella

机构信息

Department of Anatomy and Neurosciences, University of Melbourne, Melbourne, Australia.

Danish Research Institute of Translational Neuroscience, Aarhus University, Aarhus, Denmark.

出版信息

Stem Cells. 2015 Jun;33(6):1759-70. doi: 10.1002/stem.1991.

Abstract

The caudal neural plate is a distinct region of the embryo that gives rise to major progenitor lineages of the developing central and peripheral nervous system, including neural crest and floor plate cells. We show that dual inhibition of the glycogen synthase kinase 3β and activin/nodal pathways by small molecules differentiate human pluripotent stem cells (hPSCs) directly into a preneuroepithelial progenitor population we named "caudal neural progenitors" (CNPs). CNPs coexpress caudal neural plate and mesoderm markers, and, share high similarities to embryonic caudal neural plate cells in their lineage differentiation potential. Exposure of CNPs to BMP2/4, sonic hedgehog, or FGF2 signaling efficiently directs their fate to neural crest/roof plate cells, floor plate cells, and caudally specified neuroepithelial cells, respectively. Neural crest derived from CNPs differentiated to neural crest derivatives and demonstrated extensive migratory properties in vivo. Importantly, we also determined the key extrinsic factors specifying CNPs from human embryonic stem cell include FGF8, canonical WNT, and IGF1. Our studies are the first to identify a multipotent neural progenitor derived from hPSCs, that is the precursor for major neural lineages of the embryonic caudal neural tube.

摘要

尾侧神经板是胚胎中的一个独特区域,它产生发育中的中枢和外周神经系统的主要祖细胞谱系,包括神经嵴和底板细胞。我们发现,通过小分子对糖原合酶激酶3β和激活素/节点信号通路进行双重抑制,可将人多能干细胞(hPSC)直接分化为一种我们命名为“尾侧神经祖细胞”(CNP)的神经上皮前体细胞群体。CNP共表达尾侧神经板和中胚层标志物,并且在其谱系分化潜能方面与胚胎尾侧神经板细胞高度相似。将CNP暴露于BMP2/4、音猬因子或FGF2信号中,可分别有效地将其命运导向神经嵴/顶板细胞、底板细胞和尾侧特化的神经上皮细胞。源自CNP的神经嵴分化为神经嵴衍生物,并在体内表现出广泛的迁移特性。重要的是,我们还确定了从人胚胎干细胞中指定CNP的关键外在因子,包括FGF8、经典WNT和IGF1。我们的研究首次鉴定出一种源自hPSC的多能神经祖细胞,它是胚胎尾侧神经管主要神经谱系的前体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b78/5347855/eabf2f01f8db/STEM-33-1759-g001.jpg

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