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首页> 外文期刊>Developmental cell >Semaphorin-Plexin Signaling Controls Mitotic Spindle Orientation during Epithelial Morphogenesis and Repair
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Semaphorin-Plexin Signaling Controls Mitotic Spindle Orientation during Epithelial Morphogenesis and Repair

机译:Semaphorin-Plexin信号传导控制上皮细胞形态发生和修复过程中的有丝分裂纺锤方向

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摘要

Morphogenesis, homeostasis, and regeneration of epithelial tissues rely on the accurate orientation of cell divisions, which is specified by the mitotic spindle axis. To remain in the epithelial plane, symmetrically dividing epithelial cells align their mitotic spindle axis with the plane. Here, we show that this alignment depends on epithelial cell-cell communication via semaphorin-plexin signaling. During kidney morphogenesis and repair, renal tubular epithelial cells lacking the transmembrane receptor Plexin-B2 or its semaphorin ligands fail to correctly orient the mitotic spindle, leading to severe defects in epithelial architecture and function. Analyses of a series of transgenic and knockout mice indicate that Plexin-B2 controls the cell division axis by signaling through its GTPase-activating protein (GAP) domain and Cdc42. Our data uncover semaphorin-plexin signaling as a central regulatory mechanism of mitotic spindle orientation necessary for the alignment of epithelial cell divisions with the epithelial plane.
机译:上皮组织的形态发生,稳态和再生依赖于有丝分裂纺锤体轴所指定的细胞分裂的精确方向。为了保留在上皮平面中,对称分裂的上皮细胞将其有丝分裂纺锤体轴与该平面对齐。在这里,我们显示这种对齐方式取决于通过信号蛋白-plexin信号传导的上皮细胞-细胞通讯。在肾脏形态发生和修复过程中,缺乏跨膜受体Plexin-B2或其信号灯配体的肾小管上皮细胞无法正确定向有丝分裂纺锤体,从而导致上皮结构和功能的严重缺陷。一系列转基因和基因敲除小鼠的分析表明,Plexin-B2通过其GTPase激活蛋白(GAP)结构域和Cdc42发出信号来控制细胞分裂轴。我们的数据揭示了semaphorin-plexin信号作为有丝分裂纺锤体定向的中央调节机制,是上皮细胞分裂与上皮平面对齐所必需的。

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