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A Polished and Reinforced Thinned-skull Window for Long-term Imaging of the Mouse Brain

机译:抛光和加固的薄颅骨窗用于小鼠脑的长期成像

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摘要

In vivo imaging of cortical function requires optical access to the brain without disruption of the intracranial environment. We present a method to form a polished and reinforced thinned skull (PoRTS) window in the mouse skull that spans several millimeters in diameter and is stable for months. The skull is thinned to 10 to 15 μm in thickness with a hand held drill to achieve optical clarity, and is then overlaid with cyanoacrylate glue and a cover glass to: 1) provide rigidity, 2) inhibit bone regrowth and 3) reduce light scattering from irregularities on the bone surface. Since the skull is not breached, any inflammation that could affect the process being studied is greatly reduced. Imaging depths of up to 250 μm below the cortical surface can be achieved using two-photon laser scanning microscopy. This window is well suited to study cerebral blood flow and cellular function in both anesthetized and awake preparations. It further offers the opportunity to manipulate cell activity using optogenetics or to disrupt blood flow in targeted vessels by irradiation of circulating photosensitizers.
机译:皮质功能的体内成像需要在不破坏颅内环境的情况下光学进入大脑。我们提出了一种方法,该方法可以在直径超过几毫米且数月稳定的鼠标颅骨中形成抛光和加固的变薄颅骨(PoRTS)窗口。用手持钻将头骨减薄至10至15μm的厚度以实现光学清晰度,然后用氰基丙烯酸酯胶和覆盖玻璃覆盖,以:1)提供刚性,2)抑制骨骼再生,和3)减少光散射骨头表面的不规则性。由于头骨没有被破坏,因此可以影响研究过程的任何炎症都可以大大减少。使用双光子激光扫描显微镜可以实现皮层表面以下250μm的成像深度。该窗口非常适合研究麻醉和清醒制剂中的脑血流量和细胞功能。它进一步提供了利用光遗传学来操纵细胞活性或通过循环光敏剂的照射破坏靶血管中血流的机会。

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