3D super-resolution microscopy reflects mitochondrial cristae alternations and mtDNA nucleoid size and distribution
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
29727614
DOI
10.1016/j.bbabio.2018.04.013
PII: S0005-2728(18)30089-6
Knihovny.cz E-resources
- Keywords
- 3D super-resolution microscopy, ATP-synthase α subunit, Distances frequency distribution histogram, Mitochondrial cristae, Mitochondrial nucleoids, Ripley's K-function,
- MeSH
- Insulin-Secreting Cells cytology metabolism MeSH
- Hep G2 Cells MeSH
- DNA-Binding Proteins metabolism MeSH
- Microscopy, Fluorescence instrumentation MeSH
- Rats MeSH
- Cells, Cultured MeSH
- Humans MeSH
- DNA, Mitochondrial chemistry metabolism MeSH
- Mitochondrial Membranes metabolism MeSH
- Mitochondrial Proteins metabolism MeSH
- Rats, Wistar MeSH
- Imaging, Three-Dimensional methods MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- DNA-Binding Proteins MeSH
- DNA, Mitochondrial MeSH
- Mitochondrial Proteins MeSH
3D super-resolution microscopy based on the direct stochastic optical reconstruction microscopy (dSTORM) with primary Alexa-Fluor-647-conjugated antibodies is a powerful method for accessing changes of objects that could be normally resolved only by electron microscopy. Despite the fact that mitochondrial cristae yet to become resolved, we have indicated changes in cristae width and/or morphology by dSTORM of ATP-synthase F1 subunit α (F1α). Obtained 3D images were analyzed with the help of Ripley's K-function modeling spatial patterns or transferring them into distance distribution function. Resulting histograms of distances frequency distribution provide most frequent distances (MFD) between the localized single antibody molecules. In fasting state of model pancreatic β-cells, INS-1E, MFD between F1α were ~80 nm at 0 and 3 mM glucose, whereas decreased to 61 nm and 57 nm upon glucose-stimulated insulin secretion (GSIS) at 11 mM and 20 mM glucose, respectively. Shorter F1α interdistances reflected cristae width decrease upon GSIS, since such repositioning of F1α correlated to average 20 nm and 15 nm cristae width at 0 and 3 mM glucose, and 9 nm or 8 nm after higher glucose simulating GSIS (11, 20 mM glucose, respectively). Also, submitochondrial entities such as nucleoids of mtDNA were resolved e.g. after bromo-deoxyuridine (BrDU) pretreatment using anti-BrDU dSTORM. MFD in distances distribution histograms reflected an average nucleoid diameter (<100 nm) and average distances between nucleoids (~1000 nm). Double channel PALM/dSTORM with Eos-lactamase-β plus anti-TFAM dSTORM confirmed the latter average inter-nucleoid distance. In conclusion, 3D single molecule (dSTORM) microscopy is a reasonable tool for studying mitochondrion.
References provided by Crossref.org
Mitochondrial Physiology of Cellular Redox Regulations
Pitfalls of Mitochondrial Redox Signaling Research
Possible frequent multiple mitochondrial DNA copies in a single nucleoid in HeLa cells
Glucose-Induced Expression of DAPIT in Pancreatic β-Cells
Contribution of Oxidative Stress and Impaired Biogenesis of Pancreatic β-Cells to Type 2 Diabetes