Exploratory nuclear microprobe data visualisation using 3- and 4-dimensional biological volume rendering tools

Abstract The emergence of Confocal Microscopy (CM) and Atomic Force Microscopy (AFM) as everyday tools in cellular level biology has stimulated development of 3D data visualisation software. Conventional 2-dimensional images of cell (optical) sections obtained in a transmission electron or optical microscopes and more sophisticated multidimensional imaging methods require processing software capable of 3D rendering and mathematically transforming data in 3-, 4-, or more dimensions. The richness of data obtained from the different nuclear microscopy imaging techniques and often parallel information channels (X-ray, secondary electron, Scanning Transmission Ion Microscopy) is often not obvious because subtleties and interrelations in the data could not be rendered in a human interpretable way. In this exploratory study we have applied the BioImageXD software, originally developed for rendering of multidimensional CM data, to some different nuclear microscopy data. Cells-on-Silicon STIM data from a human breast cancer cell line and elemental maps from lesions on rabbit aorta have been visualised. Mathematical filtering and averaging combined with hardware accelerated 3D rendering enabled dramatically clear visualisation of inter-cellular regions comprising extra cellular matrix proteins that were otherwise difficult to visualise, and also sub cellular structures. For elemental mapping, the use of filtered correlation surfaces and colour channels clearly revealed the interrelations in the data structures that are not easily discernible in the PIXE elemental maps.

[1]  B. Halliwell,et al.  A nuclear microscopy study of trace elements Ca, Fe, Zn and Cu in atherosclerosis , 2006 .

[2]  L. Bartoshuk,et al.  Comparing sensory experiences across individuals: recent psychophysical advances illuminate genetic variation in taste perception. , 2000, Chemical senses.

[3]  H. Whitlow,et al.  Response of Si p-i-n diode and Au/n-Si surface barrier detector to heavy ions , 2002 .

[4]  A. Rosen,et al.  Scleroderma Autoantigens Are Uniquely Fragmented by Metal-catalyzed Oxidation Reactions: Implications for Pathogenesis , 1997, The Journal of experimental medicine.

[5]  Victoria J Allan,et al.  Light Microscopy Techniques for Live Cell Imaging , 2003, Science.

[6]  H. Whitlow,et al.  Energy loss measurements for mass-14 ions using a patterned stopping medium on a PIN diode , 2004 .

[7]  C. J. Tandler AN ACID-SOLUBLE COMPONENT OF THE NUCLEOLUS; THE CYTOCHEMICAL SPECIFICITY OF THE "LEAD ACETATE REACTION" , 1956, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[8]  Study of localised radiation damage to PIPS detectors by a scanning ion microprobe: Measured effects and the consequences for STIM analysis , 1997 .

[9]  I. Kottke,et al.  Subcellular localization of Cd in the root cells ofAllium sativum by electron energy loss spectroscopy , 2003, Journal of Biosciences.

[10]  J. Nielsen,et al.  Mercury-induced autoimmunity in mice. , 2002, Environmental health perspectives.

[11]  S S Stevens,et al.  On the Theory of Scales of Measurement. , 1946, Science.

[12]  Measurements of the stopping forces for heavy ions in Ge, Ag and Au using novel 'polka-dot' detectors , 2006 .

[13]  J. Aten,et al.  Measurement of co‐localization of objects in dual‐colour confocal images , 1993, Journal of microscopy.

[14]  D. Sprinzak,et al.  Scanning electron microscopy of cells and tissues under fully hydrated conditions. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[15]  Sylvain V Costes,et al.  Automatic and quantitative measurement of protein-protein colocalization in live cells. , 2004, Biophysical journal.