ICFO-Institut de Ciències Fotòniques, The Barcelona Institute of Science and Technology, 08860 Castelldefels (Barcelona), Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic c/ Villarroel 170, 08036 Barcelona, Spain.
ICFO-Institut de Ciències Fotòniques, The Barcelona Institute of Science and Technology, 08860 Castelldefels (Barcelona), Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Hospital Clínic c/ Villarroel 170, 08036 Barcelona, Spain.
Cell Rep. 2018 Jun 26;23(13):3759-3768. doi: 10.1016/j.celrep.2018.05.096.
Anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis is a severe neuropsychiatric disorder mediated by autoantibodies against the GluN1 subunit of the NMDAR. Patients' antibodies cause cross-linking and internalization of NMDAR, but the synaptic events leading to depletion of NMDAR are poorly understood. Using super-resolution microscopy, we studied the effects of the autoantibodies on the nanoscale distribution of NMDAR in cultured neurons. Our findings show that, under control conditions, NMDARs form nanosized objects and patients' antibodies increase the clustering of synaptic and extrasynaptic receptors inside the nano-objects. This clustering is subunit specific and predominantly affects GluN2B-NMDARs. Following internalization, the remaining surface NMDARs return to control clustering levels but are preferentially retained at the synapse. Monte Carlo simulations using a model in which antibodies induce NMDAR cross-linking and disruption of interactions with other proteins recapitulated these results. Finally, activation of EphB2 receptor partially antagonized the antibody-mediated disorganization of the nanoscale surface distribution of NMDARs.
抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种严重的神经精神疾病,由针对 NMDAR 的 GluN1 亚基的自身抗体介导。患者的抗体导致 NMDAR 的交联和内吞,但导致 NMDAR 耗竭的突触事件知之甚少。使用超分辨率显微镜,我们研究了自身抗体对培养神经元中 NMDAR 纳米级分布的影响。我们的研究结果表明,在对照条件下,NMDAR 形成纳米大小的物体,并且患者的抗体增加纳米物体内部突触和 extrasynaptic 受体的聚类。这种聚类是亚基特异性的,主要影响 GluN2B-NMDAR。内吞后,剩余的表面 NMDAR 回到对照聚类水平,但优先保留在突触处。使用一种模型的蒙特卡罗模拟,其中抗体诱导 NMDAR 交联和破坏与其他蛋白质的相互作用,再现了这些结果。最后,EphB2 受体的激活部分拮抗了抗体介导的 NMDAR 纳米表面分布的紊乱。