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Fluorescence microscopy timelapse dataset of PNT1A, DU-145 and LNCaP cells with annotated caspase 3,7-dependent and independent cell death

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  • Additional Information
    • Publication Information:
      Zenodo
    • Publication Date:
      2021
    • Collection:
      Zenodo
    • Abstract:
      Time-lapse dataset of prostatic cell lines (DU-145, PNT1A, LNCaP) exposed to cell death-inducing compounds (staurosporine, doxorubicin) and black phosphorus. Fluorescence dataset of correlative microscopy performed together with quantitative phase microscopy (QPI, dataset available at doi.org/10.5281/zenodo.2601562 together with annotations.The time-lapse dataset is annotated as follows: (1) cell masks and cell numbers, (2) by cell death type and timepoint of death in the attached xlsx file. This dataset is supplementary to the article: Vicar, T., Raudenska, M., Gumulec, J. et al. The Quantitative-Phase Dynamics of Apoptosis and Lytic Cell Death. Sci Rep 10, 1566 (2020). https://doi.org/10.1038/s41598-020-58474-w Code is available at https://github.com/tomasvicar/CellDeathDetect Methods Cell culture and cultured cell conditions LNCaP cell line was established from a lymph node metastase of the hormone-refractory patient and contains a mutation in the AR gene. This mutation creates a promiscuous AR that can bind to different types of steroids. LNCaP cells are AR-positive, PSA-positive, PTEN-negative and harbor wild-type p53. PNT1A is immortalized non-tumorigenic epithelial cell line. PNT1A cells harbour wild-type p53. However, SV40 induced T-antigen expression inhibits the activity of p53. This cell line had lost the expression of androgen receptor (AR) and prostate-specific antigen (PSA) (Raudenska, 2019). DU-145 cell line is derived from the metastatic site in the brain and contains P223L and V274F mutations in p53. This cell line is PSA and AR-negative and androgen independent (Chappell, 2012). All cell lines used in this study were purchased from HPA Culture Collections (Salisbury, UK). and were cultured in RPMI-1640 medium with 10 % FBS. The medium was supplemented with antibiotics (penicillin 100 U/ml and streptomycin 0.1 mg/ml). Cells were maintained at 37°C in a humidified (60%) incubator with 5% CO2 (Sanyo, Japan). Correlative time-lapse quantitative phase-fluorescence imaging QPI and fluorescence ...
    • Relation:
      https://doi.org/10.1038/s41598-020-58474-w; https://doi.org/10.5281/zenodo.2601562; https://doi.org/10.1101/589697; https://zenodo.org/communities/masariklab; https://doi.org/10.5281/zenodo.4531899; https://doi.org/10.5281/zenodo.4531900; oai:zenodo.org:4531900
    • Accession Number:
      10.5281/zenodo.4531900
    • Online Access:
      https://doi.org/10.5281/zenodo.4531900
    • Rights:
      info:eu-repo/semantics/openAccess ; Creative Commons Attribution 4.0 International ; https://creativecommons.org/licenses/by/4.0/legalcode
    • Accession Number:
      edsbas.24FB938F