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Quantitative Superresolution Microscopy Reveals Differences in Nuclear DNA Organization of Multiple Myeloma and Monoclonal Gammopathy of Undetermined Significance
Authors:Chirawadee Sathitruangsak  Christiaan H Righolt  Ludger Klewes  Pille Tammur  Tiiu Ilus  Anu Tamm  Mari Punab  Adebayo Olujohungbe  Sabine Mai
Institution:1. Manitoba Institute of Cell Biology, University of Manitoba, CancerCare Manitoba, Winnipeg, Manitoba, Canada;2. Division of Medical Oncology, Department of Internal Medicine, Prince of Songkla University, Songkhla, Thailand;3. Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands;4. Genomic Centre for Cancer Research and Diagnosis (GCCRD), Manitoba Institute of Cell Biology, CancerCare Manitoba, Winnipeg, Manitoba, Canada;5. United Laboratories, Tartu University Hospital, Tartu, Estonia;6. Hematology and Oncology Clinic, Tartu University Hospital, Tartu, Estonia;7. Department of Haematology, CancerCare Manitoba, Winnipeg, Manitoba, Canada;8. Department of Physiology, University of Manitoba, Manitoba Institute of Cell Biology, CancerCare Manitoba, Winnipeg, Manitoba, Canada
Abstract:The mammalian nucleus has a distinct substructure that cannot be visualized directly by conventional microscopy. In this study, the organization of the DNA within the nucleus of multiple myeloma (MM) cells, their precursor cells (monoclonal gammopathy of undetermined significance; MGUS) and control lymphocytes of the representative patients is visualized and quantified by superresolution microscopy. Three‐dimensional structured illumination microscopy (3D‐SIM) increases the spatial resolution beyond the limits of conventional widefield fluorescence microscopy. 3D‐SIM reveals new insights into the nuclear architecture of cancer as we show for the first time that it resolves organizational differences in intranuclear DNA organization of myeloma cells in MGUS and in MM patients. In addition, we report a significant increase in nuclear submicron DNA structure and structure of the DNA‐free space in myeloma nuclei compared to normal lymphocyte nuclei. Our study provides previously unknown details of the nanoscopic DNA architecture of interphase nuclei of the normal lymphocytes, MGUS and MM cells. This study opens new avenues to understanding the disease progression from MGUS to MM. J. Cell. Biochem. 116: 704–710, 2015. © 2014 The Authors. Journal of Cellular Biochemistry published by Wiley Periodicals, Inc.
Keywords:3D STRUCTURED ILLUMINATION MICROSCOPY  DNA NANO STRUCTURE  MULTIPLE MYELOMA  MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE
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