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Spatiotemporal expression of osteopontin in the striatum of rats subjected to the mitochondrial toxin 3-nitropropionic acid correlates with microcalcification

机译:线粒体毒素3-硝基丙酸对大鼠纹状体中骨桥蛋白的时空表达与微钙化的关系

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摘要

Our aim was to elucidate whether osteopontin (OPN) is involved in the onset of mineralisation and progression of extracellular calcification in striatal lesions due to mitochondrial toxin 3-nitropropionic acid exposure. OPN expression had two different patterns when observed using light microscopy. It was either localised to the Golgi complex in brain macrophages or had a small granular pattern scattered in the affected striatum. OPN labelling tended to increase in number and size over a 2-week period following the lesion. Ultrastructural investigations revealed that OPN is initially localised to degenerating mitochondria within distal dendrites, which were then progressively surrounded by profuse OPN on days 7–14. Electron probe microanalysis of OPN-positive and calcium-fixated neurites indicated that OPN accumulates selectively on the surfaces of degenerating calcifying dendrites, possibly via interactions between OPN and calcium. In addition, 3-dimensional reconstruction of OPN-positive neurites revealed that they are in direct contact with larger OPN-negative degenerating dendrites rather than with fragmented cell debris. Our overall results indicate that OPN expression is likely to correlate with the spatiotemporal progression of calcification in the affected striatum, and raise the possibility that OPN may play an important role in the initiation and progression of microcalcification in response to brain insults.
机译:我们的目的是阐明骨桥蛋白(OPN)是否与线粒体毒素3-硝基丙酸暴露引起的纹状体病变的矿化和细胞外钙化的进展有关。当使用光学显微镜观察时,OPN表达具有两种不同的模式。它要么位于脑巨噬细胞中的高尔基复合体中,要么散布在受影响的纹状体中。病变后2周内,OPN标签的数量和大小趋于增加。超微结构研究表明,OPN最初位于远端树突内的变性线粒体中,然后在第7-14天逐渐被大量OPN包围。电子探针对OPN阳性和钙固定神经突的显微分析表明,OPN可能通过OPN与钙之间的相互作用选择性地聚集在变性钙化树突的表面上。此外,OPN阳性神经突的3维重建显示,它们与较大的OPN阴性简并树突直接接触,而不是与碎片细胞碎片直接接触。我们的总体结果表明,OPN的表达可能与受影响的纹状体中钙化的时空进展相关,并增加了OPN可能在响应于脑损伤的微钙化的开始和进展中起重要作用。

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