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神经周网可保护培养的皮质神经元免受β-淀粉样蛋白的神经毒性作用。

Perineuronal nets protect against amyloid beta-protein neurotoxicity in cultured cortical neurons.

作者信息

Miyata Seiji, Nishimura Yousuke, Nakashima Toshihiro

机构信息

Department of Applied Biology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.

出版信息

Brain Res. 2007 May 30;1150:200-6. doi: 10.1016/j.brainres.2007.02.066. Epub 2007 Mar 2.

DOI:10.1016/j.brainres.2007.02.066
PMID:17397805
Abstract

Perineuronal nets (PNs) consisting of chondroitin sulfate proteoglycans (CSPGs) and hyaluronic acid are associated with distinct neuronal populations in mammalian brain. Cortical areas abundant in PNs have been known to be less affected by neurotoxicity in human Alzheimer's disease. In the present study, we examined whether PNs protect the neurotoxicity caused by amyloid beta-protein (Abeta), a major constituent of senile plaques in Alzheimer's disease using cortical neurons of dissociated culture. Double labeling experiments using confocal microscopy showed that the neurons associated with PNs were visualized with the anti-CSPG antibody in dissociated cortical culture. The analysis of reverse transcription-polymerase chain reaction revealed that mRNA expression of chondroitin sulfotransferases, CSPG-specific enzymes, was detected in neuronal culture, indicating that cultured cortical neurons are able to synthesize CSPGs and construct PNs structure. The treatment of Abeta1-42 showed significant neurotoxicity on PNs-free cortical neurons, however, it did not reveal neurotoxicity on PNs-associated neurons. Moreover, it was shown that the treatment of Abeta1-42 was able to kill PNs-associated neurons after the removal of chondroitin sulfate (CS) glycosaminoglycans with chondroitinase ABC. The treatment of glutamate killed not only PNs-free cortical neurons but also PNs-associated neurons. These results suggest that CS glycosaminoglycans on PNs are responsible for protecting neurons from Abeta1-42 neurotoxicity.

摘要

由硫酸软骨素蛋白聚糖(CSPGs)和透明质酸组成的神经元周围网(PNs)与哺乳动物大脑中不同的神经元群体相关。已知富含PNs的皮质区域在人类阿尔茨海默病中受神经毒性的影响较小。在本研究中,我们使用解离培养的皮质神经元,研究了PNs是否能保护由淀粉样β蛋白(Aβ)引起的神经毒性,Aβ是阿尔茨海默病老年斑的主要成分。使用共聚焦显微镜的双重标记实验表明,在解离的皮质培养物中,与PNs相关的神经元可通过抗CSPG抗体可视化。逆转录-聚合酶链反应分析显示,在神经元培养物中检测到了硫酸软骨素转移酶(CSPG特异性酶)的mRNA表达,这表明培养的皮质神经元能够合成CSPGs并构建PNs结构。Aβ1-42处理对无PNs的皮质神经元显示出显著的神经毒性,然而,对与PNs相关的神经元未显示出神经毒性。此外,研究表明,在用软骨素酶ABC去除硫酸软骨素(CS)糖胺聚糖后,Aβ1-42处理能够杀死与PNs相关的神经元。谷氨酸处理不仅杀死了无PNs的皮质神经元,也杀死了与PNs相关的神经元。这些结果表明,PNs上的CS糖胺聚糖负责保护神经元免受Aβ1-42的神经毒性。

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