In Vivo Three-Dimensional Two-Photon Microscopy to Study Conducted Vascular Responses by Local ATP Ejection Using a Glass Micro-Pipette

被引:6
作者
Cai, Changsi [1 ]
Zambach, Stefan A. [1 ]
Fordsmann, Jonas C. [1 ]
Lonstrup, Micael [1 ]
Thomsen, Kirsten J. [1 ]
Jensen, Aske G. K. [1 ]
Lauritzen, Martin [1 ,2 ]
机构
[1] Univ Copenhagen, Fac Med & Hlth Sci, Dept Neurosci, Copenhagen, Denmark
[2] Rigshosp, Dept Clin Neurophysiol, Copenhagen, Denmark
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2019年 / 148期
关键词
Neuroscience; Issue; 148; in vivo; two-photon microscopy; cerebral blood flow (CBF); astrocytes; three dimensions (3D); neurovascular coupling; calcium imaging; viral vector injection; ACTIVITY-DEPENDENT INCREASES; BLOOD-FLOW;
D O I
10.3791/59286
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Maintenance of normal brain function requires a sufficient and efficient supply of oxygen and nutrition by a complex network of vessels. However, the regulation of cerebral blood flow (CBF) is incompletely understood, especially at the capillary level. Two-photon microscopy is a powerful tool widely used to study CBF and its regulation. Currently, this field is limited by the lack of in vivo two-photon microscopy studies examining (1) CBF responses in three-dimensions, (2) conducted vascular responses, and (3) localized interventions within the vascular network. Here, we describe a 3D in vivo method using two-photon microscopy to study conducted vascular responses elicited by local ejection of ATP with a glass micropipette. Our method uses fast and repetitive hyperstack two-photon imaging providing precise diameter measurements by maximal intensity projection of the obtained images. Furthermore, we show that this method can also be used to study 3D astrocytic calcium responses. We also discuss the advantages and limitations of glass micro-pipette insertion and two-photon hyperstack imaging.
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页数:8
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