Tomographic STED microscopy to study bone resorption

We present a tomographic Stimulated Emission Depletion (STED) microscopy method with three-dimensional superresolution, and its application to osteoclast bone resorption study. In order to improve axial resolution in standard STED system by tomography, two axial projections were obtained by imaging a sample at two different angles; one conventionally from below and another from the side. The second observation was acquired via a metal-coated silicon mirror, positioned above the region of interest by a custom-built micro-positioner. The acquired two sets of 3D stacks were computationally registered and fused, with our own in-house-developed software, to produce a 3D tomogram with three-dimensional super-resolution. With the presented tomographic super-resolution method we optically investigated actin cytoskeleton through thin and smooth bone layer, particularly at ruffled boarders (RB), which are directly associated with active bone resorption in osteoclasts. Tomographic STED microscopy at RB of osteoclast, cultured on thin bone layer, demonstrated axial resolution of approx. 210 nm, revealing fine axial structures of actin cytoskeleton at RB. Further investigation of the cytoskeleton at RB in relation with associated proteins would provide understanding in the protein roles during the bone resorption.

[1]  Jeremy L O'Brien,et al.  Solid Immersion Facilitates Fluorescence Microscopy with Nanometer Resolution and Sub-Ångström Emitter Localization , 2012, Advanced materials.

[2]  T. Kuorilehto,et al.  Osteoclasts in neurofibromatosis type 1 display enhanced resorption capacity, aberrant morphology, and resistance to serum deprivation. , 2010, Bone.

[3]  F. Saltel,et al.  Actin cytoskeletal organisation in osteoclasts: a model to decipher transmigration and matrix degradation. , 2008, European journal of cell biology.

[4]  H. Väänänen,et al.  Endocytic pathway from the basal plasma membrane to the ruffled border membrane in bone-resorbing osteoclasts. , 1997, Journal of cell science.

[5]  T. Svitkina Ultrastructure of protrusive actin filament arrays. , 2013, Current opinion in cell biology.

[6]  P. De Camilli,et al.  Dynamin forms a Src kinase-sensitive complex with Cbl and regulates podosomes and osteoclast activity. , 2005, Molecular biology of the cell.

[7]  S. Hell,et al.  Fluorescence microscopy with diffraction resolution barrier broken by stimulated emission. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[8]  S. Hell,et al.  Spherical nanosized focal spot unravels the interior of cells , 2008, Nature Methods.

[9]  Sami Koho,et al.  A software tool for STED-AFM correlative super-resolution microscopy , 2015, Photonics West - Biomedical Optics.

[10]  F. Saltel,et al.  Apatite-mediated actin dynamics in resorbing osteoclasts. , 2004, Molecular biology of the cell.

[11]  H. Väänänen,et al.  Osteoclast Ruffled Border Has Distinct Subdomains for Secretion and Degraded Matrix Uptake , 2003, Traffic.

[12]  Tuomas Näreoja,et al.  Axial super-resolution by mirror-reflected stimulated emission depletion microscopy , 2014 .

[13]  T. Chambers,et al.  Distinctive Subdomains in the Resorbing Surface of Osteoclasts , 2013, PloS one.

[14]  S.W. HELL,et al.  A compact STED microscope providing 3D nanoscale resolution , 2009, Journal of microscopy.

[15]  Kenneth A. Taylor,et al.  Structural Organization of the Actin Cytoskeleton at Sites of Clathrin-Mediated Endocytosis , 2011, Current Biology.

[16]  J. Salo,et al.  Bone-resorbing osteoclasts reveal a dynamic division of basal plasma membrane into two different domains. , 1996, Journal of cell science.