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Wnt信号传导活性与Sox2转录因子水平的比值可预测神经中胚层命运潜能。

The ratio of Wnt signaling activity to Sox2 transcription factor levels predicts neuromesodermal fate potential.

作者信息

Morabito Robert D, Tatarakis David, Swick Ryan, Stettnisch Samantha, Schilling Thomas F, Horsfield Julia A, Martin Benjamin L

机构信息

Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, NY 11733, USA.

Department of Developmental and Cell Biology, University of California, Irvine, CA 92697, USA.

出版信息

bioRxiv. 2025 Jan 21:2025.01.16.633481. doi: 10.1101/2025.01.16.633481.

Abstract

Neuromesodermal progenitors (NMPs) are a vertebrate cell type that contribute descendants to both the spinal cord and the mesoderm. The undifferentiated bipotential NMP state is maintained when both Wnt signaling is active and Sox2 is present. We used transgenic reporter lines to live-image both Wnt activity and Sox2 levels in NMPs and observed a unique cellular ratio in NMPs compared to NMP-derived mesoderm or neural tissue. We used this unique signature to identify the previously unknown anatomical position of a progenitor population that gives rise to the midline tissues of the floor plate of the spinal cord and the mesodermal notochord. Thus, quantification of the active Wnt signaling to Sox2 ratio can be used to predict and identify cells with neuromesodermal potential. We also developed the auxin inducible degron 2 system for use in zebrafish to test the temporal role that Sox2 plays during midline formation. We found ectopic Sox2 in the presence of Wnt activity holds cells in the undifferentiated floor plate/notochord progenitor state, and that degradation of the ectopic Sox2 is required for cells to adopt a notochord fate.

摘要

神经中胚层祖细胞(NMPs)是一种脊椎动物细胞类型,其后代对脊髓和中胚层都有贡献。当Wnt信号活跃且Sox2存在时,未分化的双能NMP状态得以维持。我们使用转基因报告系对NMPs中的Wnt活性和Sox2水平进行活体成像,并观察到与NMP衍生的中胚层或神经组织相比,NMPs中独特的细胞比例。我们利用这一独特特征确定了一个祖细胞群体的先前未知的解剖位置,该群体产生脊髓底板和中胚层脊索的中线组织。因此,活性Wnt信号与Sox2比例的量化可用于预测和识别具有神经中胚层潜能的细胞。我们还开发了用于斑马鱼的生长素诱导降解子2系统,以测试Sox2在中线形成过程中所起的时间作用。我们发现,在Wnt活性存在的情况下,异位的Sox2会使细胞保持在未分化的底板/脊索祖细胞状态,而异位Sox2的降解是细胞采用脊索命运所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c26/11761523/f0611f2c642b/nihpp-2025.01.16.633481v2-f0001.jpg

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