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Microscope slides

Company: SuperFrost Plus
Catalog#: 631-0108
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Super-resolution Imaging of the T cell Central Supramolecular Signaling Cluster Using Stimulated Emission Depletion Microscopy
Author:
Date:
2020-11-05
[Abstract]  

Supramolecular signaling assemblies are of interest for their unique signaling properties. A µm scale signaling assembly, the central supramolecular signaling cluster (cSMAC), forms at the center interface of T cells activated by antigen presenting cells (APC). The adaptor protein linker for activation of T cells (LAT) is a key cSMAC component. The cSMAC has widely been studied using total internal reflection fluorescence microscopy of CD4+ T cells activated by planar APC substitutes. Here we provide a protocol to image the cSMAC in its cellular context at the interface between a T cell and an APC. Super resolution stimulated emission depletion microscopy (STED) was utilized to determine the localization of LAT, that of its active, phosphorylated form and its entire pool. Agonist

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[摘要]  [摘要]超分子信号组装体因其独特的信号传导特性而受到关注。在抗原呈递细胞(APC)激活的T细胞的中心界面处形成一个微米级的信号传导组件,即中央超分子信号簇(cSMAC )。用于激活T细胞(LAT)的衔接子蛋白接头是关键的cSMAC组件。所述CSMAC已被广泛使用的CD4全内反射荧光显微镜研究+由平面APC替代活化的T细胞。在这里,我们提供了一种协议,可以在T细胞和APC之间的接口在其细胞上下文中成像cSMAC 。超分辨率激发发射耗尽显微镜(STED)用于确定LA T的定位,其活性,磷酸化形式及其整个池的位置。在固定和抗体染色之前,将载有激动剂肽的APC与TCR转基因CD4 + T细胞孵育4.5分钟。固定的细胞对在Leica SP8 AOBS共聚焦激光扫描显微镜上使用100x 1.4 NA物镜成像。LAT聚集在多个超分子复合物中,并确定了它们的数量和大小分布。使用此协议,可以量化在T细胞和APC之间的界面在其细胞环境中的cSMAC属性。

[背景] ...

Staining and Quantitative Analysis of Myelinating Oligodendrocytes in the Mouse Grey Matter
Author:
Date:
2020-10-20
[Abstract]  Oligodendrocytes generate distinct patterns of myelination throughout the CNS. Variations in myelination along axons may enable neurons to fine-tune conduction velocities and alter signal synchronisation. Here we outline a staining protocol permitting the assessment of the number and length of myelin sheaths formed by oligodendrocyte in the mouse grey matter. This protocol enables the investigation of myelination without the need for reporter mice or technically challenging protocols, aiding the investigation of factors influencing myelin production in the brain. [摘要]  [摘要] 少突胶质细胞在中枢神经系统产生不同的髓鞘形成模式。轴突髓鞘的变化可能使神经元能够微调传导速度和改变信号同步。在这里,我们概述了一个染色方案,允许评估由少突胶质细胞在小鼠灰质中形成的髓鞘的数量和长度。这一方案使研究髓鞘无需报告小鼠或技术上具有挑战性的协议,有助于研究影响大脑髓鞘生成的因素。

[背景] 少突胶质细胞在中枢神经系统(CNS)轴突周围产生绝缘的髓鞘。髓鞘通过鞘间小的无髓鞘间隙处电压依赖性钠通道的浓度加速轴突传导速度——Ranvier节点(Huxley和Stampfli,1949;Rushton,1951;Waxman,1997)。尽管少突胶质细胞遍布中枢神经系统,但并非所有轴突都有髓鞘,这表明髓鞘的形成和大小可能精确地调节动作电位速度和神经元同步性(Pajevic等人,2014)。因此,了解是什么影响少突胶质细胞产生髓鞘的数量(即一个细胞形成的鞘的数量和大小)对于理解髓鞘如何改变神经元功能很重要。
许多技术已经被发展用来分析体内少突胶质细胞的复杂形态。最初,Pio del Rio Hortega的研究使用碳酸银染色法,根据形成的髓鞘的数量和长度来识别和区分少突胶质细胞(Perez ...

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