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将面投影层析成像技术与电子断层成像技术相结合,深入了解小鼠大脑皮层血脑屏障的通透性。

Combining array tomography with electron tomography provides insights into leakiness of the blood-brain barrier in mouse cortex.

机构信息

Institute of Neuronal Cell Biology, Technical University Munich, Munich, Germany.

German Center for Neurodegenerative Diseases (DZNE), Munich, Germany.

出版信息

Elife. 2024 Aug 5;12:RP90565. doi: 10.7554/eLife.90565.

Abstract

Like other volume electron microscopy approaches, automated tape-collecting ultramicrotomy (ATUM) enables imaging of serial sections deposited on thick plastic tapes by scanning electron microscopy (SEM). ATUM is unique in enabling hierarchical imaging and thus efficient screening for target structures, as needed for correlative light and electron microscopy. However, SEM of sections on tape can only access the section surface, thereby limiting the axial resolution to the typical size of cellular vesicles with an order of magnitude lower than the acquired xy resolution. In contrast, serial-section electron tomography (ET), a transmission electron microscopy-based approach, yields isotropic voxels at full EM resolution, but requires deposition of sections on electron-stable thin and fragile films, thus making screening of large section libraries difficult and prone to section loss. To combine the strength of both approaches, we developed 'ATUM-Tomo, a hybrid method, where sections are first reversibly attached to plastic tape via a dissolvable coating, and after screening detached and transferred to the ET-compatible thin films. As a proof-of-principle, we applied correlative ATUM-Tomo to study ultrastructural features of blood-brain barrier (BBB) leakiness around microthrombi in a mouse model of traumatic brain injury. Microthrombi and associated sites of BBB leakiness were identified by confocal imaging of injected fluorescent and electron-dense nanoparticles, then relocalized by ATUM-SEM, and finally interrogated by correlative ATUM-Tomo. Overall, our new ATUM-Tomo approach will substantially advance ultrastructural analysis of biological phenomena that require cell- and tissue-level contextualization of the finest subcellular textures.

摘要

与其他体积电子显微镜方法一样,自动化胶带收集超薄切片(ATUM)通过扫描电子显微镜(SEM)使沉积在厚塑料带上的连续切片成像成为可能。ATUM 的独特之处在于能够进行层次成像,从而有效地筛选目标结构,这是相关光和电子显微镜所需要的。然而,在胶带上的切片 SEM 只能访问切片表面,从而将轴向分辨率限制在细胞囊泡的典型尺寸,其数量级比所获得的 xy 分辨率低一个数量级。相比之下,基于透射电子显微镜的连续切片电子断层扫描(ET)方法可以在全 EM 分辨率下获得各向同性体素,但需要将切片沉积在电子稳定的薄而脆弱的薄膜上,因此难以筛选大的切片库并且容易丢失切片。为了结合这两种方法的优势,我们开发了“ATUM-Tomo”混合方法,其中首先通过可溶解的涂层将切片可逆地附着到塑料带上,然后在筛选后将其分离并转移到适合 ET 的薄膜上。作为原理验证,我们应用相关的 ATUM-Tomo 来研究创伤性脑损伤小鼠模型中微血栓周围血脑屏障(BBB)通透性的超微结构特征。通过注射的荧光和电子致密纳米粒子的共聚焦成像来识别微血栓和相关的 BBB 渗漏部位,然后通过 ATUM-SEM 重新定位,最后通过相关的 ATUM-Tomo 进行检测。总体而言,我们的新 ATUM-Tomo 方法将极大地推进需要对最细微的细胞纹理进行细胞和组织水平上下文化的生物现象的超微结构分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21ee/11299977/77e9b42a7e8d/elife-90565-fig1.jpg

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