Caccamo D, Katsetos C D, Herman M M, Frankfurter A, Collins V P, Rubinstein L J
Department of Pathology (Neuropathology), University of Virginia School of Medicine, Charlottesville.
Lab Invest. 1989 Mar;60(3):390-8.
Spontaneous ovarian teratomas develop in a large proportion of female LT strain mice. These tumors display a large neuroectodermal component with morphologic differentiation ranging from primitive neuroepithelium (medulloepithelial and ependymoblastic rosettes) to mature neurons, and provide a useful system for the study of various asynchronous stages of neuroepithelial differentiation. The aim of this study was to assess the expression of various cytoskeletal proteins in conjunction with other differentiation-related antigens in these tumors. We found that the medulloepithelial rosettes reacted with only two anti-beta-tubulin monoclonal antibodies. One of these (TU27) recognizes an epitope common to all of the mammalian beta-tubulin isotypes. The other monoclonal antibody (TUJ1) recognizes an epitope unique to class III beta-tubulin isotypes (neuronal-associated). Whereas immunoreactivity in the ependymoblastic rosettes was limited to TU27, differentiating polar neuroblasts reacted with both TU27 and TUJ1 and expressed neuron-specific enolase, synaptophysin, and the 68 kilodalton subunit of neurofilament protein. In well-differentiated foci, mature neurons were positive for all three neurofilament protein subunits (68, 168 and 200 kilodaltons), microtubule-associated-protein 2, synaptophysin, and neuron-specific-enolase, and reacted with both TU27 and TUJ1. By contrast, glial elements expressed glial fibrillary acidic and S-100 proteins, Leu-7 and TU27 but not TUJ1. Myelin basic protein and myelin-associated glycoprotein reactivity was found in the neuropile of these mature areas. The neuroepithelial components were negative for retinal S-antigen and cytokeratin. The expression of the class III beta-tubulin isotype by medulloepithelial rosettes suggests that this isotype may be one of the earliest markers to signal neuronal commitment in primitive neuroepithelium.
在大部分雌性 LT 品系小鼠中会自发形成卵巢畸胎瘤。这些肿瘤呈现出大量神经外胚层成分,其形态学分化范围从原始神经上皮(髓上皮和室管膜母细胞玫瑰花结)到成熟神经元,为研究神经上皮分化的不同异步阶段提供了一个有用的系统。本研究的目的是评估这些肿瘤中各种细胞骨架蛋白与其他分化相关抗原的表达情况。我们发现,髓上皮玫瑰花结仅与两种抗β-微管蛋白单克隆抗体发生反应。其中一种(TU27)识别所有哺乳动物β-微管蛋白亚型共有的一个表位。另一种单克隆抗体(TUJ1)识别 III 类β-微管蛋白亚型(神经元相关)特有的一个表位。室管膜母细胞玫瑰花结中的免疫反应仅限于 TU27,分化中的极性成神经细胞与 TU27 和 TUJ1 均发生反应,并表达神经元特异性烯醇化酶、突触素和神经丝蛋白的 68 千道尔顿亚基。在分化良好的病灶中,成熟神经元对所有三种神经丝蛋白亚基(68、168 和 200 千道尔顿)、微管相关蛋白 2、突触素和神经元特异性烯醇化酶均呈阳性反应,并与 TU27 和 TUJ1 均发生反应。相比之下,神经胶质成分表达神经胶质纤维酸性蛋白和 S-100 蛋白、Leu-7 和 TU27,但不表达 TUJ1。在这些成熟区域的神经毡中发现了髓鞘碱性蛋白和髓鞘相关糖蛋白反应性。神经上皮成分对视网膜 S 抗原和细胞角蛋白呈阴性。髓上皮玫瑰花结对 III 类β-微管蛋白亚型的表达表明,该亚型可能是原始神经上皮中指示神经元定向分化的最早标志物之一。