Cellular imaging of deep organ using two-photon Bessel light-sheet nonlinear structured illumination microscopy.

In vivo fluorescent cellular imaging of deep internal organs is highly challenging, because the excitation needs to penetrate through strong scattering tissue and the emission signal is degraded significantly by photon diffusion induced by tissue-scattering. We report that by combining two-photon Bessel light-sheet microscopy with nonlinear structured illumination microscopy (SIM), live samples up to 600 microns wide can be imaged by light-sheet microscopy with 500 microns penetration depth, and diffused background in deep tissue light-sheet imaging can be reduced to obtain clear images at cellular resolution in depth beyond 200 microns. We demonstrate in vivo two-color imaging of pronephric glomeruli and vasculature of zebrafish kidney, whose cellular structures located at the center of the fish body are revealed in high clarity by two-color two-photon Bessel light-sheet SIM.

[1]  Pierre Nassoy,et al.  Light-sheet microscopy in thick media using scanned Bessel beams and two-photon fluorescence excitation. , 2013, Optics express.

[2]  L. Zon,et al.  Transparent adult zebrafish as a tool for in vivo transplantation analysis. , 2008, Cell stem cell.

[3]  Jan Huisken,et al.  Multilayer mounting enables long-term imaging of zebrafish development in a light sheet microscope , 2012, Development.

[4]  F. Hildebrandt,et al.  Inducible podocyte injury and proteinuria in transgenic zebrafish. , 2012, Journal of the American Society of Nephrology : JASN.

[5]  Rainer Heintzmann,et al.  Saturated patterned excitation microscopy with two-dimensional excitation patterns. , 2003, Micron.

[6]  Philipp J. Keller,et al.  Fast, high-contrast imaging of animal development with scanned light sheet–based structured-illumination microscopy , 2010, Nature Methods.

[7]  Philipp J. Keller,et al.  Quantitative high-speed imaging of entire developing embryos with simultaneous multiview light-sheet microscopy , 2012, Nature Methods.

[8]  Ming Zhao,et al.  Nonlinear structured illumination microscopy by surface plasmon enhanced stimulated emission depletion. , 2011, Optics express.

[9]  Lars Hufnagel,et al.  Multiview light-sheet microscope for rapid in toto imaging , 2012, Nature Methods.

[10]  F. Del Bene,et al.  Optical Sectioning Deep Inside Live Embryos by Selective Plane Illumination Microscopy , 2004, Science.

[11]  M. Gustafsson Nonlinear structured-illumination microscopy: wide-field fluorescence imaging with theoretically unlimited resolution. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[12]  T. Wilson,et al.  Method of obtaining optical sectioning by using structured light in a conventional microscope. , 1997, Optics letters.

[13]  A. Rohrbach,et al.  Microscopy with self-reconstructing beams , 2010 .

[14]  David S. Koos,et al.  Deep and fast live imaging with two-photon scanned light-sheet microscopy , 2011, Nature Methods.

[15]  M. Davidson,et al.  Noninvasive Imaging beyond the Diffraction Limit of 3D Dynamics in Thickly Fluorescent Specimens , 2012, Cell.

[16]  Tony Wilson,et al.  Image-based adaptive optics for two-photon microscopy. , 2009, Optics letters.

[17]  Philipp J. Keller,et al.  Reconstruction of Zebrafish Early Embryonic Development by Scanned Light Sheet Microscopy , 2008, Science.