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首页> 外文期刊>The international journal of developmental biology >Regulation of Merkel cell development by Pax6
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Regulation of Merkel cell development by Pax6

机译:Pax6对默克尔细胞发育的调控

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Merkel cells are mechanoreceptors widely distributed in the vertebrate skin. In rodents, Merkel cells within the whisker pads are innervated by free sensory nerve endings derived from the maxillary branch of the trigeminal nerve. This study identified expression of the transcription factor Pax6 in Merkel cells and investigated its role. Immunohistochemistry and Western blot for Pax6 and Merkel cell markers, cytokeratin-8 (K8) and cytokeratin-20 (K20) were performed in wild-type and Pax6 ~-/- fetuses. The subcellular localisation of Pax6 in Merkel cells in vitro was manipulated using hydrogen peroxide. Pax6 was primarily localised within the cytoplasm of the Merkel cells at birth, but postnatally was also detected within the nuclei. In vitro, after 4 days in culture Pax6 protein was completely relocated to the nuclei of fetal-derived Merkel cells, mimicking the in vivo situation, suggesting that Pax6 acts as an active nucleo-cytoplasmic shuttling protein in common with many other homeodomain transcription factors. The subcellular localisation of Pax6 could be modulated in vitro by changing the redox potential of the culture medium for Merkel cells. Differentiation of cultured Pax6 ~-/- Merkel cells was shown to be inhibited. At perinatal stages, it was found that Pax6 is required for maintaining cytokeratin-8 expression, an early Merkel cell marker, whereas cytokeratin-20 was retained by the Pax6 ~-/- mutant cells. Pax6 is expressed in developing Merkel cells as a nucleo-cytoplasmic shuttling protein and its activity is required for normal differentiation, possibly through regulating cell maturation.
机译:默克尔细胞是广泛分布在脊椎动物皮肤中的机械感受器。在啮齿动物中,晶须垫内的默克尔细胞被源自三叉神经上颌支的自由感觉神经末梢支配。这项研究确定了转录因子Pax6在默克尔细胞中的表达,并研究了其作用。 Pax6和Merkel细胞标志物cytokeratin-8(K8)和cytokeratin-20(K20)的免疫组织化学和蛋白质印迹在野生型和Pax6〜-/-胎儿中进行。使用过氧化氢对Pax6在Merkel细胞体外的亚细胞定位进行了控制。 Pax6主要在出生时定位在默克尔细胞的细胞质内,但在出生后的细胞核内也检测到。在体外培养4天后,Pax6蛋白完全重定位到胎儿来源的Merkel细胞核中,模仿了体内情况,这表明Pax6与许多其他同源域转录因子一样,是一种活跃的核质穿梭蛋白。通过改变培养基对默克尔细胞的氧化还原电位,可以在体外调节Pax6的亚细胞定位。已显示培养的Pax6〜//-Merkel细胞的分化受到抑制。在围产期,发现Pax6是维持细胞角蛋白8表达(早期默克尔细胞标志物)所必需的,而细胞角蛋白20被Pax6-/-突变细胞保留。 Pax6在发育中的默克尔细胞中作为核质穿梭蛋白表达,其活性是正常分化所必需的,可能是通过调节细胞成熟来实现的。

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