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自发性大鼠星形细胞瘤和恶性网状细胞增多症的组织学和免疫组织化学研究

Histological and immunohistochemical studies on spontaneous rat astrocytomas and malignant reticulosis.

作者信息

Nagatani Mariko, Ando Ryo, Yamakawa Seiki, Saito Tsubasa, Tamura Kazutoshi

机构信息

Hamamatsu Branch of Pathology Department, Biology and Zoology Research Center Inc., Hamamatsu, Shizuoka 435-0016, Japan.

出版信息

Toxicol Pathol. 2009 Aug;37(5):599-605. doi: 10.1177/0192623309338385. Epub 2009 Jun 1.

DOI:10.1177/0192623309338385
PMID:19487256
Abstract

Among spontaneous neoplasms of the rat central nervous system, the discrimination between astrocytoma and malignant reticulosis (MR) is sometimes difficult because of their similar cell morphology and infiltration patterns. In the present study, we carried out histological and immunohistochemical analyses on a total of sixty-four cases in Sprague-Dawley and F344 rats. These cases were diagnosed as benign/malignant astrocytoma containing no neoplastic oligodendroglial elements or MR according to the diagnostic criteria of the World Health Organization International Classification of Rodent Tumors (Mohr et al. 1994). Astrocytomas were divided into three types and MR into two types based on the number of lesions, cellularity and infiltration patterns, and so on. Although the neoplastic cells from all types showed various immunoreactivities for RM-4 (anti-rat macrophages and dendritic cells), ED-1, and/or vimentin, there were no distinctive differences among these types, and most cells that were positive for RM-4 were also positive for ED-1. None of the tumor types showed any reactivity for GFAP or S-100 protein. From the results of morphological and immunohistochemical examinations, it was indicated that there are no distinctive differences between spontaneous astrocytomas and MR in rats, and they are probably derived from the same cell lineage, that is, microglia, macrophage, or radial glia.

摘要

在大鼠中枢神经系统的自发性肿瘤中,有时难以区分星形细胞瘤和恶性网状细胞增多症(MR),因为它们的细胞形态和浸润模式相似。在本研究中,我们对总共64例Sprague-Dawley和F344大鼠进行了组织学和免疫组织化学分析。根据世界卫生组织国际啮齿动物肿瘤分类的诊断标准(Mohr等人,1994年),这些病例被诊断为不含肿瘤性少突胶质细胞成分的良性/恶性星形细胞瘤或MR。根据病变数量、细胞密度和浸润模式等,将星形细胞瘤分为三种类型,将MR分为两种类型。尽管所有类型的肿瘤细胞对RM-4(抗大鼠巨噬细胞和树突状细胞)、ED-1和/或波形蛋白表现出不同的免疫反应性,但这些类型之间没有明显差异,并且大多数对RM-4呈阳性的细胞对ED-1也呈阳性。所有肿瘤类型对GFAP或S-100蛋白均无反应性。从形态学和免疫组织化学检查结果表明,大鼠自发性星形细胞瘤和MR之间没有明显差异,它们可能源自同一细胞谱系,即小胶质细胞、巨噬细胞或放射状胶质细胞。

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