Time-Lapse Imaging to Analyze Cell Fate in Response to Antimitotics

Methods Mol Biol. 2025:2874:115-126. doi: 10.1007/978-1-0716-4236-8_10.

Abstract

Time-lapse imaging is a powerful technique widely used in Cellular and Molecular Biology to capture and analyze the dynamic processes of living cells over specific time periods. Particularly, in the study of cell division, under normal conditions or after drug treatments, this methodology can provide essential data that is impossible to obtain from conventional cell-fixed-based assays. In the context of evaluating cell fate after antimitotic drug treatment, time-lapse imaging provides valuable insights into the mechanisms of action of these compounds. Antimitotic drugs belong to a class of anticancer compounds that interfere with mitosis by targeting microtubules or specific kinases and molecular motors involved in the mitotic apparatus. This chapter aims to highlight the significant advantage of using time-lapse microscopy to assess the effects of antimitotic drugs on cell behavior and fates. We describe the full protocol for time-lapse imaging, using the human lung adenocarcinoma A549 cell line as a model, after exposure to the antimitotic BI2536, a potent inhibitor of polo-like kinase 1 (PLK1). This description includes software for imaging acquisition and data analysis.

Keywords: Antimitotic agents; BI2536; Cell dynamics; Cell fate; Cell tracking; Polo-like kinase 1; Time-lapse imaging.

MeSH terms

  • A549 Cells
  • Antimitotic Agents* / pharmacology
  • Cell Cycle Proteins / metabolism
  • Cell Line, Tumor
  • Humans
  • Image Processing, Computer-Assisted / methods
  • Mitosis* / drug effects
  • Polo-Like Kinase 1
  • Protein Serine-Threonine Kinases* / antagonists & inhibitors
  • Protein Serine-Threonine Kinases* / metabolism
  • Proto-Oncogene Proteins / antagonists & inhibitors
  • Proto-Oncogene Proteins / metabolism
  • Pteridines / pharmacology
  • Time-Lapse Imaging* / methods

Substances

  • Antimitotic Agents
  • Protein Serine-Threonine Kinases
  • Polo-Like Kinase 1
  • BI 2536
  • Pteridines
  • Cell Cycle Proteins
  • Proto-Oncogene Proteins