Please use this identifier to cite or link to this item:
https://biore.bio.bg.ac.rs/handle/123456789/5411| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pajić, Tanja | en_US |
| dc.contributor.author | Todorović, Nataša | en_US |
| dc.contributor.author | Živić, Miroslav | en_US |
| dc.contributor.author | Nikolić, Stanko | en_US |
| dc.contributor.author | Rabasović, Mihailo | en_US |
| dc.contributor.author | Clayton, Andrew H. A. | en_US |
| dc.contributor.author | Krmpot, Aleksandar | en_US |
| dc.date.accessioned | 2023-03-01T10:55:48Z | - |
| dc.date.available | 2023-03-01T10:55:48Z | - |
| dc.date.issued | 2022-11-05 | - |
| dc.identifier.issn | 2045-2322 | - |
| dc.identifier.uri | https://biore.bio.bg.ac.rs/handle/123456789/5411 | - |
| dc.description.abstract | We report the utilization of Third-Harmonic Generation microscopy for label-free live cell imaging of lipid droplets in the hypha of filamentous fungus Phycomyces blakesleeanus. THG microscopy images showed bright spherical features dispersed throughout the hypha cytoplasm in control conditions and a transient increase in the number of bright features after complete nitrogen starvation. Colocalization analysis of THG and lipid-counterstained images disclosed that the cytoplasmic particles were lipid droplets. Particle Size Analysis and Image Correlation Spectroscopy were used to quantify the number density and size of lipid droplets. The two analysis methods both revealed an increase from 16 × 10−3 to 23 × 10−3 lipid droplets/µm2 after nitrogen starvation and a decrease in the average size of the droplets (range: 0.5–0.8 µm diameter). In conclusion, THG imaging, followed by PSA and ICS, can be reliably used for filamentous fungi for the in vivo quantification of lipid droplets without the need for labeling and/or fixation. In addition, it has been demonstrated that ICS is suitable for THG microscopy. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Springer | en_US |
| dc.relation.ispartof | Scientific Reports | en_US |
| dc.subject | Biological fluorescence | en_US |
| dc.subject | Biological physics | en_US |
| dc.subject | Biophotonics | en_US |
| dc.subject | Biophysics | en_US |
| dc.subject | Cellular imaging | en_US |
| dc.subject | Fat metabolism | en_US |
| dc.subject | Fluorescence imaging | en_US |
| dc.subject | Fungal biology | en_US |
| dc.subject | Fungal physiology | en_US |
| dc.subject | Fungi | en_US |
| dc.subject | Imaging | en_US |
| dc.subject | Imaging studies | en_US |
| dc.subject | Imaging techniques | en_US |
| dc.subject | Lipids | en_US |
| dc.subject | Microscopy | en_US |
| dc.subject | Multiphoton microscopy | en_US |
| dc.subject | Nonlinear optics | en_US |
| dc.subject | Optical imaging | en_US |
| dc.subject | Organelles | en_US |
| dc.title | Label-free third harmonic generation imaging and quantification of lipid droplets in live filamentous fungi | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | 10.1038/s41598-022-23502-4 | - |
| dc.description.rank | M21 | en_US |
| dc.description.impact | 4,997 | en_US |
| dc.description.startpage | 18760 | en_US |
| dc.description.volume | 12 | en_US |
| dc.description.issue | 1 | en_US |
| item.grantfulltext | none | - |
| item.languageiso639-1 | en | - |
| item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
| item.cerifentitytype | Publications | - |
| item.openairetype | Article | - |
| item.fulltext | No Fulltext | - |
| crisitem.author.dept | Chair of General Physiology and Biophysics | - |
| crisitem.author.dept | Chair of General Physiology and Biophysics | - |
| crisitem.author.orcid | 0000-0003-3794-7655 | - |
| crisitem.author.orcid | 0000-0002-0314-5032 | - |
| crisitem.author.parentorg | Institute of Physiology and Biochemistry "Ivan Djaja" | - |
| crisitem.author.parentorg | Institute of Physiology and Biochemistry "Ivan Djaja" | - |
| Appears in Collections: | Journal Article | |
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