IN VIVO MEASUREMENTS OF BLOOD FLOW AND GLIAL CELL FUNCTION WITH TWO-PHOTON LASER-SCANNING MICROSCOPY

被引:27
作者
Helmchen, Fritjof [1 ]
Kleinfeld, David [2 ]
机构
[1] Univ Zurich, Brain Res Inst, Dept Neurophysiol, Zurich, Switzerland
[2] Univ Calif San Diego, Dept Phys, La Jolla, CA 92093 USA
来源
ANGIOGENESIS: IN VIVO SYSTEMS, PT A | 2008年 / 444卷
基金
美国国家科学基金会; 美国国家卫生研究院; 瑞士国家科学基金会;
关键词
D O I
10.1016/S0076-6879(08)02810-3
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Two-photon laser scanning microscopy is an ideal too for high-resolution fluorescence imaging in intact organs of living animals. With regard to in vivo brain research, this technique provides new opportunities to study hemodynamics in the microvascular system and morphological dynamics and calcium signaling in various glial cell types. These studies benefit from the ongoing developments for in vivo labeling, imaging, and photostimulation. Here, we review recent advances in the application of two-photon microscopy for the study of blood flow and glial cell function in the neocortex. We emphasize the dual role of two-photon imaging as a means to assess function in the normal state as well as a tool. to investigate the vascular system and glia under pathological conditions, such as ischemia and microvascular disease. Further, we show how extensions of ultra-fast laser techniques lead to new models of stroke, where individual vessels may be targeted for occlusion with micrometer precision.
引用
收藏
页码:231 / 254
页数:24
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