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Tyrosinase and nestin immunohistochemical expression in melanocytic nevi as a histopathologic pattern to trace melanocyte differentiation and nevogenesis

机译:酪蛋白酶和巢蛋白免疫组织化学表达,Melanocytic Nevi作为追踪黑素细胞分化和鼻炎的组织病理学模式

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摘要

While histological analysis represents a powerful tool for the classification of melanocytic lesions as benign or malignant, a clear-cut distinction between a nevus and a melanoma is sometimes a challenging step of the diagnostic process. The immunohistochemical detection of tyrosinase, cardinal melanogenic enzyme during melanocytic maturation, has often been helpful in formulating a differential diagnosis due to the peculiar staining pattern in nevocytes compared with melanoma cells. Tyrosinase distribution in nevi appears to overlap with the cytoarchitectural changes observable within these lesions, that result in epidermal or superficial dermal nevocytes being larger and strongly expressing melanocytic differentiation antigens, such as tyrosinase, compared with deeper dermal nevus cells. Our study aimed to evaluate the immunohistochemical expression pattern of tyrosinase in different histological types of acquired dysplastic melanocytic nevi, including junctional, compound, and intradermal nevi. Moreover, to estimate whether in nevocytes the expression of tyrosinase was associated with their differentiation state, we investigated the expression of two recognized markers of pluripotency, CD34 and nestin. In all examined nevi, our analysis revealed a remarkable immunoreactivity for tyrosinase in junctional and superficial dermal nevocytes and a decreasing gradient of staining in dermal nevocytes, up to become negative in deeper dermis. Meanwhile, junctional and dermal nevocytes were lacking in CD34 protein. Furthermore, nestin immunostaining showed an opposite distribution compared with tyrosinase, leading us to look into the tyrosinase/nestin expression pattern in melanocytic nevus as a tool to better understand the final stages of differentiation of melanocyte precursors toward their ultimate anatomical site into the epidermis.
机译:虽然组织学分析代表了良性或恶性的黑素细胞病变分类的强大工具,但痣和黑素瘤之间的清晰区别有时是诊断过程的具有挑战性的步骤。酪氨酸酶的免疫组织化学检测在黑素细胞成熟过程中的酪氨酸酶,主要糖酵母酶,由于与黑素瘤细胞相比,由于鼻细胞中的特殊染色模式而产生差异诊断。奈维中的酪氨酸酶分布似乎与这些病变中可观察到的细胞体建筑变化重叠,这导致表皮或浅表皮肤鼻细胞更大且强烈地表达酪氨酸酶,例如酪氨酸酶,与更深的皮肤痣细胞相比。我们的研究旨在评估不同组织学类型的酪氨酸酶的免疫组织化学表达模式,其采用的消化性发育塑性骨细胞痣的不同组织学类型,包括结型,化合物和皮内奈良。此外,为了估计在痣中是否在术中酪氨酸酶的表达与其分化状态有关,我们研究了两种公认的多能性,CD34和巢蛋白的识别标志物的表达。在所有检查的奈维中,我们的分析显示了连接和浅表性皮肤痣中酪氨酸酶的显着免疫反应性,并且在皮肤痣中的染色梯度降低,在更深的真皮中变为阴性。同时,CD34蛋白质缺乏连接和皮肤的鼻腔。此外,与酪氨酸酶相比,巢蛋白免疫抑制显示出相反的分布,导致我们将酪氨酸酶中的酪氨酸酶/巢蛋白表达模式作为一种工具,以更好地理解黑素细胞前体的差异朝向其最终解剖部位进入表皮的工具。

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