Protocol In vivo two-photon microscopy protocol for imaging microglial responses and spine elimination at sites of fibrinogen deposition in mouse brain

被引:4
|
作者
Tognatta, Reshmi [1 ,2 ]
Merlini, Mario [2 ]
Yan, Zhaoqi [1 ,2 ]
Schuck, Renaud [1 ,2 ]
Davalos, Dimitrios [3 ,4 ]
Akassoglou, Katerina [1 ,2 ,5 ]
机构
[1] Gladstone UCSF Ctr Neurovasc Brain Immunol, San Francisco, CA 94158 USA
[2] Gladstone Inst Neurol Dis, San Francisco, CA 94158 USA
[3] Cleveland Clin, Lerner Res Inst, Dept Neurosci, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Lerner Coll Med, Dept Mol Med, Cleveland Clin, Cleveland, OH 44195 USA
[5] Univ Calif San Francisco, Weill Inst Neurosci, Dept Neurol, San Francisco, CA 94158 USA
来源
STAR PROTOCOLS | 2021年 / 2卷 / 03期
基金
瑞士国家科学基金会;
关键词
Immunology; Microscopy; Model Organisms; Neuroscience;
D O I
10.1016/j.xpro.2021.100638
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Deposition of the blood coagulation factor fibrinogen in the central nervous system is a hallmark of neurological diseases with blood-brain barrier disruption. We describe in vivo two-photon imaging of microglial responses and neuronal spine elimination to either intracortical microinjection of fibrinogen in healthy mice or to endogenously labeled fibrinogen deposits in Alzheimer's disease mice. This protocol allows the longitudinal study of glial and neuronal responses to blood proteins and can be used to test drug efficacy at the neurovascular interface. For complete details on the use and execution of this protocol, please refer to Davalos et al. (2012), Ryu et al. (2018), and Merlini et al. (2019).
引用
收藏
页数:20
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