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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:对大鼠纹纹岩中骨桥蛋白的时尚表达与线粒体毒素3-硝基丙酸的大鼠括约肌相关与微钙化相关

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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:我们的宗旨是阐明骨偶联蛋白(OPN)是否参与矿化病变中细胞外钙化的崩溃和进展引起的,由于线粒体毒素3-硝基丙酮酸暴露。在使用光学显微镜观察时,OPN表达有两种不同的模式。它归类于脑巨噬细胞的高尔基综合体,或者在受影响的纹状体中散落的小粒状图案。 OPN标记趋于在病变后的2周内增加数量和大小。超微结构的研究表明,OPN最初局限于远端树枝状内部的剥落线粒体,然后在第7-14天逐渐被丰富的OPN逐渐包围。 OPN-阳性和钙固定神经肌肤的电子探针微分析表明,OPN在重新生成钙化树枝状物的表面上选择性地积累,可能通过OPN和钙之间的相互作用。此外,OPN阳性神经势簇的三维重建揭示它们与较大的OPN阴性退化树突而不是用碎片的细胞碎片直接接触。我们的总体结果表明,OPN表达可能与受影响的纹状体中的钙化的时空进展相关,并提高OPN可能在微钙化的起始和进展中发挥重要作用的可能性,以应对脑损伤。

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