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. 2022 Jan 7;22:12. doi: 10.1186/s12935-021-02366-0

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 2 — Morphological features. Transmission electron microscopy of BJeLR cells treated with DMSO (10 h), erastin (37 mM, 10 h), staurosporine (STS, 0.75 mM, 8 h), H₂O₂ (16 mM, 1 h), and rapamycin (Rap, 100 nM, 24 h). Single white arrowheads, shrunken mitochondria; paired white arrowheads, chromatin condensation; black arrowheads, cytoplasmic and organelle swelling and plasma membrane rupture; black arrow, formation of double-membrane vesicles. A minimum of 10 cells per treatment condition were examined