JN Information on EB 2010
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


J Neurophysiol (December 10, 2003). doi:10.1152/jn.01007.2003
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
91/4/1908    most recent
01007.2003v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Levene, M. J.
Right arrow Articles by Webb, W. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Levene, M. J.
Right arrow Articles by Webb, W. W.
Submitted on October 20, 2003
Accepted on December 1, 2003

In vivo multiphoton microscopy of deep brain tissue

Michael J. Levene1, Daniel A. Dombeck1, Karl A. Kasischke1, Raymond P. Molloy1, and Watt W. Webb1*

1 Applied and Engineering Physics, Cornell University, Ithaca, NY, USA

* To whom correspondence should be addressed. E-mail: www2{at}cornell.edu.

Although fluorescence microscopy has proven to be one of the most powerful tools in biology, its application to the intact animal has been limited to imaging several hundred microns below the surface. The rest of the animal has eluded investigation at the microscopic level without excising tissue or performing extensive surgery. However, the ability to image with subcellular resolution in the intact animal enables a contextual setting that may be critical for understanding proper function. Clinical applications such as disease diagnosis and optical biopsy may benefit from minimally invasive in vivo approaches. Gradient index (GRIN) lenses with needle-like dimensions can transfer high-quality images many centimeters from the object plane. Here, we show that multiphoton microscopy through GRIN lenses enables minimally invasive, subcellular resolution several millimeters in the anesthetized, intact animal, and we present in vivo images of cortical layer V and hippocampus in anesthetized Thy1-YFP line H mouse. Microangiographies from deep capillaries and blood vessels containing fluorescein-dextran and quantum dot labeled serum in wild-type mouse brain are also demonstrated.




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
T. H. Chia and M. J. Levene
Microprisms for In Vivo Multilayer Cortical Imaging
J Neurophysiol, August 1, 2009; 102(2): 1310 - 1314.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A. Nimmerjahn
Astrocytes going live: advances and challenges
J. Physiol., April 15, 2009; 587(8): 1639 - 1647.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
N. Kuga, T. Hirata, I. Sakai, Y. Tanikawa, H. Y. Chiou, T. Kitanishi, N. Matsuki, and Y. Ikegaya
Rapid and local autoregulation of cerebrovascular blood flow: a deep-brain imaging study in the mouse
J. Physiol., February 15, 2009; 587(4): 745 - 752.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
K. Deisseroth, G. Feng, A. K. Majewska, G. Miesenbock, A. Ting, and M. J. Schnitzer
Next-Generation Optical Technologies for Illuminating Genetically Targeted Brain Circuits
J. Neurosci., October 11, 2006; 26(41): 10380 - 10386.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. Yao, D. R. Larson, H. D. Vishwasrao, W. R. Zipfel, and W. W. Webb
Blinking and nonradiant dark fraction of water-soluble quantum dots in aqueous solution
PNAS, October 4, 2005; 102(40): 14284 - 14289.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
D. Zenisek
Vesicle reuse revisited
PNAS, May 24, 2005; 102(21): 7407 - 7408.
[Full Text] [PDF]


Home page
PhysiologyHome page
G. E. Stutzmann and I. Parker
Dynamic Multiphoton Imaging: A Live View from Cells to Systems
Physiology, February 1, 2005; 20(1): 15 - 21.
[Abstract] [Full Text] [PDF]


Home page
Circ. Res.Home page
M. Rubart
Two-Photon Microscopy of Cells and Tissue
Circ. Res., December 10, 2004; 95(12): 1154 - 1166.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
J. C. Jung, A. D. Mehta, E. Aksay, R. Stepnoski, and M. J. Schnitzer
In Vivo Mammalian Brain Imaging Using One- and Two-Photon Fluorescence Microendoscopy
J Neurophysiol, November 1, 2004; 92(5): 3121 - 3133.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
M. Brecht, M. S. Fee, O. Garaschuk, F. Helmchen, T. W. Margrie, K. Svoboda, and P. Osten
Novel Approaches to Monitor and Manipulate Single Neurons In Vivo
J. Neurosci., October 20, 2004; 24(42): 9223 - 9227.
[Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
S. X. Lin and F. R. Maxfield
Fluorescence imaging in living animals. Focus on "Uptake and trafficking of fluorescent conjugates of folic acid in intact kidney determined using intravital two-photon microscopy"
Am J Physiol Cell Physiol, August 1, 2004; 287(2): C257 - C259.
[Full Text] [PDF]


Home page
J. Neurosci.Home page
A. Mizrahi, J. C. Crowley, E. Shtoyerman, and L. C. Katz
High-Resolution In Vivo Imaging of Hippocampal Dendrites and Spines
J. Neurosci., March 31, 2004; 24(13): 3147 - 3151.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Visit Other APS Journals Online
Copyright © 2003 by the The American Physiological Society.