Image filtering for two-photon deep imaging of lymphonodes

Michele Caccia, Laura Sironi, Maddalena Collini, Giuseppe Chirico, Ivan Zanoni, Francesca Granucci

Research output: Contribution to journalArticle

Abstract

Non-linear excitation microscopy is considered an ideal spectroscopic method for imaging thick tissues in vivo due to the reduced scattering of infrared radiation. Although imaging has been reported on brain neocortex at 600-800 μm of depth, much less uniform tissues, such as lymphonodes, are characterized by highly anisotropic light scattering that limits the penetration length. We show that the most severe limitation for deep imaging of lymphonodes appears to be the tissue scattering and the diffuse fluorescence emission of labeled cell (lymphocytes) in layers above the focusing plane. We report a study of the penetration depth of the infrared radiation in a model system and in ex vivo lymphonodes and discuss the possibility to apply Fourier filtering to the images in order to improve the observation depth.

Original languageEnglish
Pages (from-to)979-987
Number of pages9
JournalEuropean Biophysics Journal
Volume37
Issue number6
DOIs
Publication statusPublished - Jul 2008

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Keywords

  • Fluorescence
  • Non-linear spectroscopy
  • Scattering

ASJC Scopus subject areas

  • Biophysics

Cite this

Caccia, M., Sironi, L., Collini, M., Chirico, G., Zanoni, I., & Granucci, F. (2008). Image filtering for two-photon deep imaging of lymphonodes. European Biophysics Journal, 37(6), 979-987. https://doi.org/10.1007/s00249-008-0323-y