Hirose T, Scheithauer B W, Lopes M B, Gerber H A, Altermatt H J, Hukee M J, VandenBerg S R, Charlesworth J C
Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Acta Neuropathol. 1995;90(4):387-99. doi: 10.1007/BF00315012.
The cellular nature of the giant eosinophilic cells of tuber and of the cells comprising subependymal giant cell astrocytoma (SEGA) in tuberous sclerosis (TS) remains unclear. To assess the characteristics of these lesions, 13 tubers and 6 SEGA were immunohistochemically studied with glial and neuron-associated antigens. In addition to conventional ultrastructure, 6 tubers and 8 SEGA were subjected to immunoelectron microscopic study for glial fibrillary acidic protein (GFAP) and somatostatin. Eosinophilic giant cells of tubers were positive for vimentin (100%), GFAP (77%) and S-100 protein (92%); such cells were also found to a various extent to be reactive for neuron-associated antigens, including neurofilament (NF) proteins (38%) or class III beta-tubulin (77%). SEGA also showed variable immunoreactivity for GFAP (50%) or for S-100 protein (100%); NF epitopes, class III beta-tubulin, and calbindin 28-kD were expressed in 2 (33%), 5 (83%) and 4 (67%) cases, respectively. Cytoplasmic staining for somatostatin (50%), met-enkephalin (50%), 5-hydroxytryptamine (33%), beta-endorphin (33%) and neuropeptide Y (17%) was noted in SEGA, but not in tubers. Ultrastructurally, the giant cells of tubers and the cells of SEGA contained numerous intermediate filaments, frequent lysosomes and occasional rectangular or rhomboid membrane-bound crystalloids exhibiting lamellar periodicity and structural transition to lysosomes. Some SEGA cells showed features suggestive of neuronal differentiation, including stacks of rough endoplasmic reticulum, occasional microtubules and a few dense-core granules. Furthermore, in one case of tuber, a process of a single large cell was seen to be engaged in synapse formation. Intermediate filaments within a few cells of both lesions were decorated by gold particle-labeled GFAP antiserum. Within the tumor cells of SEGA, irregular, non-membrane-bound, electron-lucent areas often contained somatostatin-immunoreactive particles, whereas the latter could not be detected in tuber. The present study provides further evidence of divergent glioneuronal differentiation, both in the giant cells of tubers and the cells of SEGA. The findings of similar cells at different sites, including the subependymal zone, white matter ("heterotopias"), and cortex indirectly supports the idea that these lesions of TS result from a migration abnormality.
结节性硬化症(TS)中结节的巨大嗜酸性细胞以及构成室管膜下巨细胞星形细胞瘤(SEGA)的细胞的细胞性质仍不清楚。为了评估这些病变的特征,我们用神经胶质和神经元相关抗原对13个结节和6个SEGA进行了免疫组织化学研究。除了传统的超微结构研究外,我们还对6个结节和8个SEGA进行了针对胶质纤维酸性蛋白(GFAP)和生长抑素的免疫电子显微镜研究。结节的嗜酸性巨细胞波形蛋白阳性率为100%,GFAP阳性率为77%,S-100蛋白阳性率为92%;这些细胞在不同程度上还对包括神经丝(NF)蛋白(38%)或III类β微管蛋白(77%)在内的神经元相关抗原呈反应性。SEGA对GFAP(50%)或S-100蛋白(100%)也表现出不同的免疫反应性;NF表位、III类β微管蛋白和钙结合蛋白28-kD分别在2例(33%)、5例(83%)和4例(67%)中表达。SEGA中观察到生长抑素(50%)、甲硫氨酸脑啡肽(50%)、5-羟色胺(33%)、β-内啡肽(33%)和神经肽Y(17%)的细胞质染色,但结节中未观察到。超微结构上,结节的巨细胞和SEGA的细胞含有大量中间丝、频繁的溶酶体以及偶尔出现的呈层状周期性且向溶酶体发生结构转变的长方形或菱形膜结合晶体。一些SEGA细胞表现出提示神经元分化的特征,包括粗面内质网堆叠、偶尔的微管和一些致密核心颗粒。此外,在1例结节中,可见单个大细胞的一个突起参与突触形成。两个病变的少数细胞内的中间丝被金颗粒标记的GFAP抗血清标记。在SEGA的肿瘤细胞内,不规则的、无膜结合的电子透亮区常含有生长抑素免疫反应性颗粒,而在结节中未检测到后者。本研究进一步证明了结节的巨细胞和SEGA的细胞存在不同的神经胶质神经元分化。在包括室管膜下区、白质(“异位灶”)和皮质在内的不同部位发现相似细胞,间接支持了TS的这些病变是由迁移异常导致的观点。