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All-optical histology using ultrashort laser pulses.
Tsai, Philbert S; Friedman, Beth; Ifarraguerri, Agustin I; Thompson, Beverly D; Lev-Ram, Varda; Schaffer, Chris B; Xiong, Qing; Tsien, Roger Y; Squier, Jeffrey A; Kleinfeld, David.
Affiliation
  • Tsai PS; Department of Physics, University of California, San Diego, La Jolla, CA 92093, USA.
Neuron ; 39(1): 27-41, 2003 Jul 03.
Article in En | MEDLINE | ID: mdl-12848930
As a means to automate the three-dimensional histological analysis of brain tissue, we demonstrate the use of femtosecond laser pulses to iteratively cut and image fixed as well as fresh tissue. Cuts are accomplished with 1 to 10 microJ pulses to ablate tissue with micron precision. We show that the permeability, immunoreactivity, and optical clarity of the tissue is retained after pulsed laser cutting. Further, samples from transgenic mice that express fluorescent proteins retained their fluorescence to within microns of the cut surface. Imaging of exogenous or endogenous fluorescent labels down to 100 microm or more below the cut surface is accomplished with 0.1 to 1 nJ pulses and conventional two-photon laser scanning microscopy. In one example, labeled projection neurons within the full extent of a neocortical column were visualized with micron resolution. In a second example, the microvasculature within a block of neocortex was measured and reconstructed with micron resolution.
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Collection: 01-internacional Database: MEDLINE Main subject: Histocytological Preparation Techniques / Artifacts / Microscopy, Confocal / Lasers Limits: Animals Language: En Journal: Neuron Journal subject: NEUROLOGIA Year: 2003 Type: Article Affiliation country: United States
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Collection: 01-internacional Database: MEDLINE Main subject: Histocytological Preparation Techniques / Artifacts / Microscopy, Confocal / Lasers Limits: Animals Language: En Journal: Neuron Journal subject: NEUROLOGIA Year: 2003 Type: Article Affiliation country: United States