平面细胞极性(PCP)和Wnt信号在肾脏疾病中的作用

Athina Ganner, Soeren Lienkamp, Gerd Walz
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引用次数: 0

摘要

功能失调的纤毛引起肾囊肿。大多数纤毛是上皮细胞上表达的非运动(原代)微管细胞器,被认为将全局位置信号转化为平面细胞极性(PCP),这是一种归因于非规范Wnt信号传导的途径。PCP通路似乎通过引导上皮细胞沿发育中的肾小管轴线分裂的纺锤轴(定向细胞分裂)和/或通过协调细胞迁移和嵌入(在脊椎动物原肠胚形成过程中观察到的一种形态发生程序)来确保肾脏的正常发育。PCP信号需要一组最初在果蝇中被鉴定为PCP核心蛋白的蛋白质。目前的一些观察结果表明,完整的纤毛发生和纤毛功能需要PCP蛋白的存在,而核心PCP蛋白的亚细胞定位不受纤毛缺陷的影响。此外,纤毛缺陷可能通过PCP通路控制的增强细胞嵌入来克服,开辟了潜在的令人兴奋的防止囊肿形成的新途径。
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Planar cell polarity (PCP) and Wnt signaling in renal disease

Dysfunctional cilia cause kidney cysts. Most cilia are non-motile (primary) microtubular organelles expressed on epithelial cells that are thought to translate global positional cues into planar cell polarity (PCP), a pathway ascribed to non-canonical Wnt signaling. The PCP pathways then seem to ensure normal renal development by orienting the spindle axis of dividing epithelial cells along the axis of the developing kidney tubule (oriented cell division), and/or by orchestrating cell migration and intercalation, a morphogenetic program observed during vertebrate gastrulation (convergent extension). PCP signaling requires a set of proteins originally identified as PCP core proteins in Drosophila. Several observations now suggest that intact ciliogenesis and ciliary functions require the presence of PCP proteins, while the subcellular localization of core PCP proteins is not affected by ciliary defects. Furthermore, ciliary defects may be overcome by enhanced cell intercalation controlled by the PCP pathway, opening potentially exciting new avenues to prevent cyst formation.

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