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首页> 外文期刊>Nature Communications >Cerebrospinal fluid-derived Semaphorin3B orients neuroepithelial cell divisions in the apicobasal axis
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Cerebrospinal fluid-derived Semaphorin3B orients neuroepithelial cell divisions in the apicobasal axis

机译:脑脊液来源的Semaphorin3B定向于上oba后轴神经上皮细胞分裂

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摘要

The spatial orientation of cell divisions is fundamental for tissue architecture and homeostasis. Here we analysed neuroepithelial progenitors in the developing mouse spinal cord to determine whether extracellular signals orient the mitotic spindle. We report that Semaphorin3B ( Sema3B ) released from the floor plate and the nascent choroid plexus in the cerebrospinal fluid (CSF) controls progenitor division orientation. Delivery of exogenous Sema3B to neural progenitors after neural tube opening in living embryos promotes planar orientation of their division. Preventing progenitor access to cues present in the CSF by genetically engineered canal obstruction affects the proportion of planar and oblique divisions. Sema3B knockout phenocopies the loss of progenitor access to the CSF. Sema3B binds to the apical surface of mitotic progenitors and exerts its effect via Neuropilin receptors, GSK3 activation and subsequent inhibition of the microtubule stabilizer CRMP2 . Thus, extrinsic control mediated by the Semaphorin signalling orients progenitor divisions in neurogenic zones.
机译:细胞分裂的空间方向是组织结构和体内平衡的基础。在这里,我们分析了发育中的小鼠脊髓中的神经上皮祖细胞,以确定细胞外信号是否定向有丝分裂纺锤体。我们报告Semaphorin3B(Sema3B)从地板和脑脊髓液(CSF)中新生的脉络丛中释放控制祖细胞分裂方向。在活胚中的神经管打开后,将外源Sema3B传递至神经祖细胞会促进其分裂的平面方向。通过基因工程的管阻塞来阻止祖细胞接近存在于CSF中的提示会影响平面和倾斜分隔的比例。 Sema3B基因敲除表型显示祖细胞无法进入CSF。 Sema3B与有丝分裂祖细胞的顶端表面结合,并通过Neuropilin受体,GSK3激活和随后对微管稳定剂CRMP2的抑制而发挥作用。因此,由Semaphorin信号传导介导的外部控制定向了神经源性区域中的祖细胞分裂。

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