In vivo deep tissue fluorescence imaging of the murine small intestine and colon

Recently we described a novel technical approach with enhanced fluorescence detection capabilities in two-photon microscopy that achieves deep tissue imaging, while maintaining micron resolution. This technique was applied to in vivo imaging of murine small intestine and colon. Individuals with Inflammatory Bowel Disease (IBD), commonly presenting as Crohn's disease or Ulcerative Colitis, are at increased risk for developing colorectal cancer. We have developed a Giα2 gene knock out mouse IBD model that develops colitis and colon cancer. The challenge is to study the disease in the whole animal, while maintaining high resolution imaging at millimeter depth. In the Giα2-/- mice, we have been successful in imaging Lgr5-GFP positive stem cell reporters that are found in crypts of niche structures, as well as deeper structures, in the small intestine and colon at depths greater than 1mm. In parallel with these in vivo deep tissue imaging experiments, we have also pursued autofluorescence FLIM imaging of the colon and small intestine-at more shallow depths (roughly 160μm)- on commercial two photon microscopes with excellent structural correlation (in overlapping tissue regions) between the different technologies.

[1]  Min Gu,et al.  Penetration depth of single-, two-, and three-photon fluorescence microscopic imaging through human cortex structures: Monte Carlo simulation. , 2003, Applied optics.

[2]  A. Welch,et al.  A review of the optical properties of biological tissues , 1990 .

[3]  T. Wilson,et al.  Scanning two photon fluorescence microscopy with extended depth of field , 2006 .

[4]  K. Fujita [Two-photon laser scanning fluorescence microscopy]. , 2007, Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme.

[5]  M. H. Ross,et al.  Histology: A Text and Atlas: With Correlated Cell and Molecular Biology. Eighth Edition, 2018 Authors: Wojciech Pawlina; Michael H. Ross , 2019, Morphologia.

[6]  Winfried Denk,et al.  On the fundamental imaging-depth limit in two-photon microscopy , 2004, SPIE Photonics Europe.

[7]  Enrico Gratton,et al.  Enhancement of imaging depth in turbid media using a wide area detector , 2011, Journal of biophotonics.

[8]  H. Gerritsen,et al.  Imaging of optically thick specimen using two‐photon excitation microscopy , 1999, Microscopy research and technique.

[9]  Christophe Odin,et al.  Out-of-focus fluorescence collection in two-photon microscopy of scattering media , 2008 .

[10]  Jerome Mertz,et al.  Two-photon microscopy in brain tissue: parameters influencing the imaging depth , 2001, Journal of Neuroscience Methods.

[11]  H. Clevers,et al.  Identification of stem cells in small intestine and colon by marker gene Lgr5 , 2007, Nature.

[12]  D. O'Malley,et al.  Chapter 5: Imaging in depth: controversies and opportunities. , 2008, Methods in cell biology.

[13]  I. Yaroslavsky,et al.  Optical properties of selected native and coagulated human brain tissues in vitro in the visible and near infrared spectral range. , 2002, Physics in medicine and biology.

[14]  W. Denk,et al.  Two-photon imaging to a depth of 1000 microm in living brains by use of a Ti:Al2O3 regenerative amplifier. , 2003, Optics letters.

[15]  Enrico Gratton,et al.  Mitigating thermal mechanical damage potential during two-photon dermal imaging. , 2004, Journal of biomedical optics.

[16]  Hans Clevers,et al.  Crypt stem cells as the cells-of-origin of intestinal cancer , 2009, Nature.

[17]  Aernout Kisteman,et al.  Comparison of penetration depth between two-photon excitation and single-photon excitation in imaging through turbid tissue media , 2000 .