Literature DB >> 20615019

Multiphoton microscopy of cleared mouse organs.

Sonia G Parra1, Thomas H Chia, Joseph P Zinter, Michael J Levene.   

Abstract

Typical imaging depths with multiphoton microscopy (MPM) are limited to less than 300 mum in many tissues due to light scattering. Optical clearing significantly reduces light scattering by replacing water in the organ tissue with a fluid having a similar index of refraction to that of proteins. We demonstrate MPM of intact, fixed, cleared mouse organs with penetration depths and fields of view in excess of 2 mm. MPM enables the creation of large 3-D data sets with flexibility in pixel format and ready access to intrinsic fluorescence and second-harmonic generation. We present high-resolution images and 3-D image stacks of the brain, small intestine, large intestine, kidney, lung, and testicle with image sizes as large as 4,096 x 4,096 pixels.

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Year:  2010        PMID: 20615019     DOI: 10.1117/1.3454391

Source DB:  PubMed          Journal:  J Biomed Opt        ISSN: 1083-3668            Impact factor:   3.170


  17 in total

1.  Three-dimensional imaging of small intestine morphology using non-linear optical microscopy and endogenous signals.

Authors:  Clément Ricard; Barbara Vacca; Pascal Weber
Journal:  J Anat       Date:  2012-06-15       Impact factor: 2.610

2.  Optical properties of mouse brain tissue after optical clearing with FocusClear™.

Authors:  Austin J Moy; Bernard V Capulong; Rolf B Saager; Matthew P Wiersma; Patrick C Lo; Anthony J Durkin; Bernard Choi
Journal:  J Biomed Opt       Date:  2015       Impact factor: 3.170

3.  The use of optical clearing and multiphoton microscopy for investigation of three-dimensional tissue-engineered constructs.

Authors:  Elizabeth A Calle; Sam Vesuna; Sashka Dimitrievska; Kevin Zhou; Angela Huang; Liping Zhao; Laura E Niklason; Michael J Levene
Journal:  Tissue Eng Part C Methods       Date:  2014-01-16       Impact factor: 3.056

4.  Scale: a chemical approach for fluorescence imaging and reconstruction of transparent mouse brain.

Authors:  Hiroshi Hama; Hiroshi Kurokawa; Hiroyuki Kawano; Ryoko Ando; Tomomi Shimogori; Hisayori Noda; Kiyoko Fukami; Asako Sakaue-Sawano; Atsushi Miyawaki
Journal:  Nat Neurosci       Date:  2011-08-30       Impact factor: 24.884

5.  Objective, comparative assessment of the penetration depth of temporal-focusing microscopy for imaging various organs.

Authors:  Christopher J Rowlands; Oliver T Bruns; Moungi G Bawendi; Peter T C So
Journal:  J Biomed Opt       Date:  2015-06       Impact factor: 3.170

6.  Multiphoton microscopy of cleared mouse brain expressing YFP.

Authors:  Sonia G Parra; Sam S Vesuna; Teresa A Murray; Michael J Levene
Journal:  J Vis Exp       Date:  2012-09-23       Impact factor: 1.355

Review 7.  Dynamic multiphoton microscopy: focusing light on acute kidney injury.

Authors:  Andrew M Hall; Bruce A Molitoris
Journal:  Physiology (Bethesda)       Date:  2014-09

8.  PICS: a platform for planar imaging of curved surfaces of brain and other tissue.

Authors:  Jessica L Scoggin; Benjamin S Kemp; Daniel A Rivera; Teresa A Murray
Journal:  Brain Struct Funct       Date:  2019-03-22       Impact factor: 3.270

9.  In vivo imaging of Lgr5-positive cell populations using confocal laser endomicroscopy during early colon tumorigenesis.

Authors:  Jin Woo Choi; Jun Ki Kim; Myunghwan Choi; Yi Rang Kim; Seok Hyun Yun
Journal:  Endoscopy       Date:  2014-09-12       Impact factor: 10.093

10.  Optical clearing of small intestine for three-dimensional visualization of cellular proliferation within crypts.

Authors:  Jason A Kaufman; Monica J Castro; Noemy Sandoval-Skeet; Layla Al-Nakkash
Journal:  J Anat       Date:  2017-10-01       Impact factor: 2.610

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