Lagalwar Sarita, Berry Robert W, Binder Lester I
Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, 303 E. Chicago Ave, Chicago, IL 60611, USA.
Acta Neuropathol. 2007 Jan;113(1):63-73. doi: 10.1007/s00401-006-0159-4. Epub 2006 Nov 7.
Protein misfolding is a distinguishing feature of a number of neurodegenerative diseases. Accumulation of misfolded protein often results in cellular lesions, the location of lesions correlating with the nature of symptoms. Alzheimer's disease (AD), Progressive Supranuclear Palsy (PSP), Corticobasal Degeneration (CBD) and Pick's Disease (PiD) all present with pathological lesions containing hyperphosphorylated filamentous tau protein; however, the location and type of lesion varies. In addition, granulovacuolar degeneration (GVD) bodies have been reported within hippocampal pyramidal neurons in AD, PSP, CBD and PiD tissue. GVDs are defined as electron-dense granules within double membrane-bound cytoplasmic vacuoles. We have previously reported that the phosphorylated form of stress-activated protein kinase/c-Jun N-terminal kinase (p-SAPK/JNK) accumulates in granules within hippocampal pyramidal cell bodies in AD tissue at the time that hyperphosphorylated tau begins to aggregate into early-stage NFTs. We now report that p-SAPK/JNK granules are found within the hippocampal CA1 region of PSP, CBD and PiD cases as well and that these granules are likely GVD bodies. Quantitatively, p-SAPK/JNK granules and GVDs are found in comparable numbers of CA1 cells. Within cells, p-SAPK/JNK granules are distributed throughout the cytoplasm in a manner similar to the distribution of GVDs and a subset of granules co-localize with GVD markers. Ultrastructurally, p-SAPK/JNK granules are located in large cytoplasmic vacuoles, thereby fitting the definition of a GVD body. With the implication of granular p-SAPK/JNK as a marker of GVDs, our study strongly suggests that a heterogeneous group of proteins form GVDs. The mechanism of GVD formation is therefore an interesting one, and is likely separate and distinct from the mechanism of tau inclusion formation.
蛋白质错误折叠是许多神经退行性疾病的一个显著特征。错误折叠蛋白质的积累通常会导致细胞损伤,损伤的位置与症状的性质相关。阿尔茨海默病(AD)、进行性核上性麻痹(PSP)、皮质基底节变性(CBD)和皮克病(PiD)都存在含有高度磷酸化丝状tau蛋白的病理损伤;然而,损伤的位置和类型各不相同。此外,在AD、PSP、CBD和PiD组织的海马锥体细胞内已报道存在颗粒空泡变性(GVD)小体。GVD被定义为双膜结合细胞质空泡内的电子致密颗粒。我们之前曾报道,在高度磷酸化的tau开始聚集成早期神经原纤维缠结(NFTs)时,应激激活蛋白激酶/c-Jun氨基末端激酶(p-SAPK/JNK)的磷酸化形式会在AD组织的海马锥体细胞体的颗粒中积累。我们现在报告,在PSP、CBD和PiD病例的海马CA1区也发现了p-SAPK/JNK颗粒,并且这些颗粒可能是GVD小体。从数量上看,在相当数量的CA1细胞中发现了p-SAPK/JNK颗粒和GVDs。在细胞内,p-SAPK/JNK颗粒以类似于GVDs的分布方式分布在整个细胞质中,并且一部分颗粒与GVD标记物共定位。在超微结构上,p-SAPK/JNK颗粒位于大的细胞质空泡中,因此符合GVD小体的定义。由于颗粒状p-SAPK/JNK作为GVDs的标志物,我们的研究强烈表明一组异质性蛋白质形成了GVDs。因此,GVD形成的机制是一个有趣的问题,并且可能与tau包涵体形成的机制不同且相互独立。