Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892-1414, USA.
J Neurosurg. 2011 Oct;115(4):789-95. doi: 10.3171/2011.5.JNS11451. Epub 2011 Jun 17.
Astrocytomas and oligodendrogliomas are primary CNS tumors that remain a challenge to differentiate histologically because of their morphological variability and because there is a lack of reliable differential diagnostic markers. To identify proteins that are differentially expressed between astrocytomas and oligodendrogliomas, the authors analyzed the proteomic expression patterns and identified uniquely expressed proteins in these neoplasms.
Proteomes of astrocytomas and oligodendrogliomas were analyzed using 2D gel electrophoresis and subsequent computerized gel analysis to detect differentially expressed proteins. The proteins were identified using high-performance liquid chromatography accompanied by tandem mass spectrometry. To determine the role of the differentially expressed proteins in astrocytes, undifferentiated glial cell cultures were treated with dibutyryl-cyclic adenosine monophosphate (cAMP).
Two-dimensional gel electrophoresis revealed that glutamine synthetase was differentially expressed in astrocytomas and oligodendrogliomas. Western blot and immunohistochemical analyses confirmed the increased expression of glutamine synthetase in astrocytomas compared with oligodendrogliomas. Whereas glutamine synthetase expression was demonstrated across all grades of astrocytomas (Grade II-IV [15 tumors]) and oligoastrocytomas (4 tumors), it was expressed in only 1 oligodendroglioma (6% [16 tumors]). Treatment of undifferentiated glial cell cultures with dibutyryl-cAMP resulted in astrocyte differentiation that was associated with increased levels of glial fibrillary acidic protein and glutamine synthetase.
These data indicate that glutamine synthetase expression can be used to distinguish astrocytic from oligodendroglial tumors and may play a role in the pathogenesis of astrocytomas.
星形细胞瘤和少突胶质细胞瘤是原发性中枢神经系统肿瘤,由于其形态学的可变性以及缺乏可靠的鉴别诊断标志物,在组织学上仍然难以区分。为了鉴定星形细胞瘤和少突胶质细胞瘤之间差异表达的蛋白质,作者分析了蛋白质组的表达模式,并鉴定了这些肿瘤中独特表达的蛋白质。
使用二维凝胶电泳和随后的计算机凝胶分析来分析星形细胞瘤和少突胶质细胞瘤的蛋白质组,以检测差异表达的蛋白质。使用高效液相色谱法结合串联质谱法鉴定蛋白质。为了确定差异表达的蛋白质在星形胶质细胞中的作用,未分化的神经胶质细胞培养物用二丁酰环腺苷单磷酸(cAMP)处理。
二维凝胶电泳显示谷氨酰胺合成酶在星形细胞瘤和少突胶质细胞瘤中差异表达。Western blot 和免疫组织化学分析证实星形细胞瘤中谷氨酰胺合成酶的表达高于少突胶质细胞瘤。谷氨酰胺合成酶的表达在所有星形细胞瘤(2 级-IV 级[15 个肿瘤])和少突星形细胞瘤(4 个肿瘤)中均可见,而在 1 个少突胶质细胞瘤(6%[16 个肿瘤])中仅见表达。用二丁酰环腺苷单磷酸处理未分化的神经胶质细胞培养物导致星形细胞分化,同时伴有神经胶质纤维酸性蛋白和谷氨酰胺合成酶水平的升高。
这些数据表明,谷氨酰胺合成酶的表达可用于区分星形细胞瘤和少突胶质细胞瘤,并且可能在星形细胞瘤的发病机制中起作用。