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.
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Authors | Chirawadee Sathitruangsak, Christiaan H Righolt, Ludger Klewes, Pille Tammur, Tiiu Ilus, Anu Tamm, Mari Punab, Adebayo Olujohungbe, Sabine Mai |
Journal | Journal of cellular biochemistry
(J Cell Biochem)
Vol. 116
Issue 5
Pg. 704-10
(May 2015)
ISSN: 1097-4644 [Electronic] United States |
PMID | 25501803
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2014 Wiley Periodicals, Inc. |
Chemical References |
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Topics |
- Aged
- Aged, 80 and over
- Cell Line, Tumor
- Cell Nucleus
(ultrastructure)
- DNA
(ultrastructure)
- Humans
- Lymphocytes
(ultrastructure)
- Microscopy
- Middle Aged
- Monoclonal Gammopathy of Undetermined Significance
(genetics, pathology)
- Multiple Myeloma
(genetics, pathology)
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