The detection of autophagic vesicles in interphase cells is well characterized with markers such as LC3, SQSTM1 (also known as p62) and LAMP2, which are commonly used in immunofluorescence and biochemistry assays to evaluate the status of autophagy in adherent cells. During mitosis, cells undergo important morphological changes which alter the position of the central plane, therefore the imaging of dividing cells has to be specifically designed. Here, we describe a method to label and image autophagic vesicles in mitotic cells to systematically analyze their number, morphology and distribution.
Keywords: Adherent cells; Autophagy; Image analysis; Immunofluorescence; Lysosomes; Mitosis; Radial plot.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.