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钙离子/钙调蛋白依赖性蛋白激酶IIα簇与稳定的脂筏相关,其形成会捕获突触后密度蛋白95(PSD-95)。

Ca2+/calmodulin-dependent protein kinase IIalpha clusters are associated with stable lipid rafts and their formation traps PSD-95.

作者信息

Suzuki Tatsuo, Du Feng, Tian Qing-Bao, Zhang Jingping, Endo Shogo

机构信息

Department of Neuroplasticity, Research Institute on Aging and Adaptation, Shinshu University Graduate School of Medicine, Matsumoto, Japan.

出版信息

J Neurochem. 2008 Feb;104(3):596-610. doi: 10.1111/j.1471-4159.2007.05035.x. Epub 2007 Nov 14.

Abstract

Relatively large number of post-synaptic density (PSD) proteins, including Ca2+/calmodulin-dependent protein kinase II (CaMKII), have the potential to associate with lipid rafts. We in this study demonstrate that the CaMKIIalpha clusters induced by ionomycin in human embryonic kidney 293 cells, as well as unclustered CaMKIIalpha (Du F., Saitoh F., Tian Q. B., Miyazawa S., Endo S. and Suzuki T, 2006, Biochem. Biophys. Res. Commun 347, 814-820), were associated with lipid rafts. The CaMKIIalpha clusters associated with lipid raft fraction became resistant to treatment with methyl-beta-cyclodextrin and subsequent cold Triton X-100, which suggests the stabilization of CaMKIIalpha cluster-associated lipid rafts. Next, we found that PSD-95, which is also a component of lipid raft fraction and does not interact directly with CaMKII, was trapped by stable CaMKIIalpha cluster-containing structure. Association of PSD-95 with CaMKIIalpha clusters was also observed in cultured neuronal cells. These results suggest the CaMKIIalpha clusters associated with the lipid rafts in the cytoplasmic region play a role in the assembly and stabilization of certain PSD proteins that have the potential to associate with lipid rafts.

摘要

包括钙/钙调蛋白依赖性蛋白激酶II(CaMKII)在内,相当数量的突触后致密区(PSD)蛋白都有可能与脂筏结合。在本研究中,我们证明了离子霉素在人胚肾293细胞中诱导形成的CaMKIIα簇,以及未聚集的CaMKIIα(Du F., Saitoh F., Tian Q. B., Miyazawa S., Endo S.和Suzuki T, 2006, Biochem. Biophys. Res. Commun 347, 814 - 820),都与脂筏相关。与脂筏部分相关的CaMKIIα簇对用甲基-β-环糊精处理以及随后的冷Triton X-100具有抗性,这表明CaMKIIα簇相关脂筏的稳定。接下来,我们发现同样作为脂筏部分成分且不直接与CaMKII相互作用的PSD-95,被含有稳定CaMKIIα簇的结构捕获。在培养的神经元细胞中也观察到了PSD-95与CaMKIIα簇的结合。这些结果表明,在细胞质区域与脂筏相关的CaMKIIα簇在某些有可能与脂筏结合的PSD蛋白的组装和稳定中发挥作用。

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