Immunohistochemical investigations of the human palatine tonsil from surgical specimens using polyclonal and monoclonal antikeratin antibodies.

A Favre, P Baracchini, A Giampalmo, F Rossi
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Abstract

The keratinization process of tonsillary epithelium in patients with different age, who underwent surgery because of chronic inflammatory processes, has been studied by employing low (40 KD), medium (52-56-58 KD), high (56-64 and 68 KD) as well as broad spectrum antikeratin antibodies. The findings thus obtained outline the various keratin patterns of the tonsil in the outer covering and, even more, in the crypt labyrinth wall. These findings have been compared with those obtained by histochemical reactions for acid phosphatase and non-specific esterase activities (Favrz et al. 1986 II). In crypt epithelium keratinization, 56-64 KD keratins are involved in cells where also high enzymic activities are taking place, namely 1. in those elements delimiting the lumen as well as in those belonging to the reticulum mesh which are nearest to it and host lymphoid elements active in immunity reactions; 2. in elements at the bottom of small and large crypts, where excavation continues into the lymphoid tissue and interfollicular spaces. 68 KD keratin, although present in lower amounts, is synthesized almost everywhere, but only irregularly. It marks surface epithelium surrounding some dermal papillae, some meshes of the crypt reticulum, the "gallery" bottom as well as elements of interfollicular proliferation developing in the lymphoid tissue like arborescence. The path of congested blood vessels in the crypt wall towards the surface is marked by keratinized epitheliocytes. 56-64 KD keratin is present in the most superficial elements and is generally accompanied by the wall growing thinner, its blistering and breaking. The most frequent pathologic alterations of the epithelium (like cellular hypertrophy) involve variations in cytoplasm keratin pattern, in still un-flattened polyhedral elements of the intermediate layers.

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用多克隆和单克隆抗角蛋白抗体对手术标本中人腭扁桃体进行免疫组化研究。
采用低(40 KD)、中(52-56-58 KD)、高(56-64和68 KD)以及广谱抗角蛋白抗体,研究了因慢性炎症过程而接受手术的不同年龄患者扁桃体上皮的角化过程。因此,这些发现勾勒出了扁桃体在外层覆盖层,甚至在隐窝迷宫壁上的各种角蛋白模式。这些发现与酸性磷酸酶和非特异性酯酶活性的组织化学反应结果进行了比较(Favrz et al. 1986 II)。在隐窝上皮角化过程中,56-64 KD角化蛋白参与了高酶活性发生的细胞,即1。在那些划分管腔的元素以及那些属于最靠近管腔的网状结构的元素中以及在免疫反应中活跃的宿主淋巴细胞;2. 在大小隐窝底部的元素中,在那里挖掘继续进入淋巴组织和滤泡间间隙。68 KD角蛋白虽然含量较低,但几乎在任何地方都有合成,但只是不规则的。它标志着一些真皮乳头周围的表面上皮,隐窝网的一些网,“画廊”底部以及淋巴组织中滤泡间增生的元素,如树突。隐窝壁上充血的血管向表面的路径被角质化的上皮细胞所标记。56-64 KD角蛋白存在于最表层的元素中,通常伴随着壁变薄、起泡和破裂。上皮最常见的病理改变(如细胞肥大)包括细胞质角蛋白模式的改变,中间层的多面体元素仍未变平。
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