Molecular Neurophysiology and Biophysics Section, Program in Developmental Neuroscience, Eunice Kennedy Shriver National Institute of Child Health and Human Development, 35 Lincoln Drive, MSC 3715, Building 35, Room 3C-905, Bethesda, MD, 20892-3715, USA.
Advanced Imaging Core, National Institute on Deafness and Other Communication Disorders, Bethesda, MD, 20892-3715, USA.
Acta Neuropathol Commun. 2020 Nov 23;8(1):197. doi: 10.1186/s40478-020-01065-7.
In addition to its role as an auxiliary subunit of A-type voltage-gated K channels, we have previously reported that the single transmembrane protein Dipeptidyl Peptidase Like 6 (DPP6) impacts neuronal and synaptic development. DPP6-KO mice are impaired in hippocampal-dependent learning and memory and exhibit smaller brain size. Using immunofluorescence and electron microscopy, we report here a novel structure in hippocampal area CA1 that was significantly more prevalent in aging DPP6-KO mice compared to WT mice of the same age and that these structures were observed earlier in development in DPP6-KO mice. These novel structures appeared as clusters of large puncta that colocalized NeuN, synaptophysin, and chromogranin A. They also partially labeled for MAP2, and with synapsin-1 and VGluT1 labeling on their periphery. Electron microscopy revealed that these structures are abnormal, enlarged presynaptic swellings filled with mainly fibrous material with occasional peripheral, presynaptic active zones forming synapses. Immunofluorescence imaging then showed that a number of markers for aging and especially Alzheimer's disease were found as higher levels in these novel structures in aging DPP6-KO mice compared to WT. Together these results indicate that aging DPP6-KO mice have increased numbers of novel, abnormal presynaptic structures associated with several markers of Alzheimer's disease.
除了作为 A 型电压门控 K 通道的辅助亚基之外,我们之前还报道过单一跨膜蛋白二肽基肽酶 6(DPP6)会影响神经元和突触的发育。DPP6-KO 小鼠在海马依赖性学习和记忆方面存在缺陷,并且大脑体积较小。通过免疫荧光和电子显微镜,我们在这里报告了海马 CA1 区域的一种新结构,与同龄 WT 小鼠相比,DPP6-KO 小鼠中这种结构更为普遍,并且在 DPP6-KO 小鼠的发育过程中更早出现。这些新结构表现为大的点状簇,与 NeuN、突触小泡蛋白和嗜铬粒蛋白 A 共定位。它们也部分标记了 MAP2,并且在外周部分与突触素-1 和 VGluT1 标记。电子显微镜显示这些结构异常,扩大的突触前肿胀充满了主要的纤维状物质,偶尔有周边的突触前活性区形成突触。免疫荧光成像随后表明,与 WT 相比,在衰老的 DPP6-KO 小鼠中,这些新结构中存在许多与衰老和特别是阿尔茨海默病相关的标志物,其水平更高。这些结果表明,衰老的 DPP6-KO 小鼠具有更多与几种阿尔茨海默病标志物相关的新型异常突触前结构。