Improved in vivo two-photon imaging after blood replacement by perfluorocarbon

被引:30
|
作者
Haiss, F. [1 ]
Jolivet, R. [1 ]
Wyss, M. T. [1 ]
Reichold, J. [2 ]
Braham, N. B. [3 ,4 ]
Scheffold, F. [3 ,4 ]
Krafft, M. P. [5 ]
Weber, B. [1 ]
机构
[1] Univ Zurich, Inst Pharmacol & Toxicol, CH-8091 Zurich, Switzerland
[2] ETH, Inst Fluid Dynam, CH-8091 Zurich, Switzerland
[3] Univ Fribourg, Dept Phys, CH-1700 Fribourg, Switzerland
[4] Univ Fribourg, Fribourg Ctr Nanomat, CH-1700 Fribourg, Switzerland
[5] Univ Strasbourg, Inst Charles Sadron, CNRS, F-67034 Strasbourg, France
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2009年 / 587卷 / 13期
基金
瑞士国家科学基金会;
关键词
MICROSCOPY; DYNAMICS;
D O I
10.1113/jphysiol.2009.169474
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Two-photon microscopy is a powerful method in biomedical research that allows functional and anatomical imaging at a subcellular resolution in vivo. The technique is seriously hampered by absorption and scattering of light by blood, which prevents imaging through large vessels. Here, we demonstrate in the rat cerebral cortex that blood replacement by perfluorocarbon emulsion, a compound also used in human critical care medicine, yields superior image quality, while preserving neuronal integrity. Shadows of large superficial vessels disappear completely and cells can be imaged underneath them. For the first time, it is possible to image complete populations of neurons and astrocytes in the upper layers of neocortex in vivo.
引用
收藏
页码:3153 / 3158
页数:6
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