Shih Andy Y, Mateo Celine, Drew Patrick J, Tsai Philbert S, Kleinfeld David
Department of Physics, University of California-San Diego, CA, USA.
J Vis Exp. 2012 Mar 7(61):3742. doi: 10.3791/3742.
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.
对皮质功能进行体内成像需要在不破坏颅内环境的情况下实现对大脑的光学通路。我们提出了一种在小鼠颅骨上形成抛光加固薄颅骨(PoRTS)窗口的方法,该窗口直径达数毫米且数月内保持稳定。用手持钻头将颅骨厚度减至10至15微米以实现光学清晰度,然后用氰基丙烯酸酯胶水和盖玻片覆盖,目的是:1)提供刚性,2)抑制骨再生,3)减少骨表面不规则处的光散射。由于颅骨未被穿透,可极大减少可能影响所研究过程的任何炎症。使用双光子激光扫描显微镜可实现皮质表面以下达250微米的成像深度。此窗口非常适合在麻醉和清醒状态下的制剂中研究脑血流量和细胞功能。它还提供了利用光遗传学操纵细胞活性或通过照射循环光敏剂破坏靶向血管中血流的机会。