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结节性硬化症2信使核糖核酸及其蛋白产物结节蛋白在正常人类大脑及结节性硬化症患者脑损伤中的定位

Localization of tuberous sclerosis 2 mRNA and its protein product tuberin in normal human brain and in cerebral lesions of patients with tuberous sclerosis.

作者信息

Kerfoot C, Wienecke R, Menchine M, Emelin J, Maize J C, Welsh C T, Norman M G, DeClue J E, Vinters H V

机构信息

Department of Pathology and Laboratory Medicine (Neuropathology), UCLA Medical Center 90095, USA.

出版信息

Brain Pathol. 1996 Oct;6(4):367-75. doi: 10.1111/j.1750-3639.1996.tb00866.x.

Abstract

Tuberous sclerosis (TSC), an autosomal dominant disorder, is characterized by malformations, hamartomas and tumors in various organs including the brain. TSC is genetically linked to two loci: TSC1 on chromosome 9q34 and TSC2 on 16p13.3. TSC2 has been cloned, sequenced and encodes a protein (tuberin) which functions as a tumor suppressor. We have analyzed the distribution of TSC2 mRNA and tuberin in the brains of TSC patients and non-affected individuals using both autopsy and biopsy material. High levels of transcript and protein expression were observed in choroid plexus epithelium, ependymal cells, most brainstem and spinal cord motor neurons, Purkinje cells and the external granule cell layer of the cerebellum in both TSC and control cases. Individual balloon cells from TSC patients showed very faint expression while other glia showed no expression of either transcript or tuberin. Neocortical and hippocampal neurons expressed high levels of TSC2 transcript, but only modest levels of tuberin. The internal granule cell layer of the cerebellum expressed abundant transcript but low levels of tuberin. These observations suggest either that tuberin expression is controlled at the level of both transcription and translation or the antibody and in-situ hybridization recognize different splice variants of the TSC2 gene. In TSC patients, dysmorphic cytomegalic neurons expressed high levels of tuberin and transcript, particularly when in an 'ectopic' location. Individual cells within subependymal giant cell astrocytomas (SEGAs) and hamartomas from TSC patients expressed moderate to high levels of TSC2 transcript and tuberin. While the TSC2 transcript is widely expressed primarily within neurons, tuberin is demonstrable primarily within dysplastic/cytomegalic cells of the cortex and subependymal hamartomas/SEGAs. CNS expression of tuberin is unique in that primarily non-dividing cells express it in this location, whereas extra-CNS expression of tuberin is mainly found in actively proliferating cell types such as epithelium.

摘要

结节性硬化症(TSC)是一种常染色体显性疾病,其特征为包括脑在内的多个器官出现畸形、错构瘤和肿瘤。TSC在基因上与两个位点相关联:9号染色体q34上的TSC1和16号染色体p13.3上的TSC2。TSC2已被克隆、测序,并编码一种作为肿瘤抑制因子发挥作用的蛋白质(结节蛋白)。我们使用尸检和活检材料分析了TSC患者及未患病个体大脑中TSC2 mRNA和结节蛋白的分布情况。在TSC患者和对照病例的脉络丛上皮、室管膜细胞、大多数脑干和脊髓运动神经元、浦肯野细胞以及小脑的外颗粒细胞层中均观察到高水平的转录本和蛋白表达。TSC患者的单个气球样细胞表达非常微弱,而其他神经胶质细胞则未表达转录本或结节蛋白。新皮质和海马神经元表达高水平的TSC2转录本,但仅表达适度水平的结节蛋白。小脑的内颗粒细胞层表达丰富的转录本,但结节蛋白水平较低。这些观察结果表明,要么结节蛋白的表达在转录和翻译水平均受到控制,要么抗体和原位杂交识别的是TSC2基因的不同剪接变体。在TSC患者中,发育异常的巨细胞神经元表达高水平的结节蛋白和转录本,尤其是当它们处于“异位”位置时。TSC患者的室管膜下巨细胞星形细胞瘤(SEGA)和错构瘤中的单个细胞表达中度至高水平的TSC2转录本和结节蛋白。虽然TSC2转录本主要在神经元内广泛表达,但结节蛋白主要在皮质和室管膜下错构瘤/SEGA的发育异常/巨细胞中表达。结节蛋白在中枢神经系统的表达具有独特性,即主要是不分裂的细胞在该部位表达它,而结节蛋白在中枢神经系统外的表达主要见于如上皮等活跃增殖的细胞类型中。

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