Selective elimination of pluripotent stem cells by PIKfyve specific inhibitors.

Stem Cell Reports

National Institute of Child Health & Human Development, National Institutes of Health, Bldg. 6A/3A15, 6 Center Drive, Bethesda, MD 20892-2790, USA. Electronic address:

Published: February 2022

AI Article Synopsis

  • PIKfyve inhibitors selectively target and kill pluripotent embryonal carcinoma cells (ECCs) and stem cells while leaving differentiated cells unharmed.
  • These inhibitors disrupt lysosome function, leading to autophagosome build-up and reduced cell growth in both pluripotent and differentiated cells.
  • In animal studies, the specific inhibitor WX8 prevented teratocarcinoma formation from ECCs and effectively eliminated pluripotent cells while allowing differentiated cells to continue growing, highlighting its potential therapeutic applications.

Article Abstract

Inhibition of PIKfyve phosphoinositide kinase selectively kills autophagy-dependent cancer cells by disrupting lysosome homeostasis. Here, we show that PIKfyve inhibitors can also selectively eliminate pluripotent embryonal carcinoma cells (ECCs), embryonic stem cells, and induced pluripotent stem cells under conditions where differentiated cells remain viable. PIKfyve inhibitors prevented lysosome fission, induced autophagosome accumulation, and reduced cell proliferation in both pluripotent and differentiated cells, but they induced death only in pluripotent cells. The ability of PIKfyve inhibitors to distinguish between pluripotent and differentiated cells was confirmed with xenografts derived from ECCs. Pretreatment of ECCs with the PIKfyve specific inhibitor WX8 suppressed their ability to form teratocarcinomas in mice, and intraperitoneal injections of WX8 into mice harboring teratocarcinoma xenografts selectively eliminated pluripotent cells. Differentiated cells continued to proliferate, but at a reduced rate. These results provide a proof of principle that PIKfyve specific inhibitors can selectively eliminate pluripotent stem cells in vivo as well as in vitro.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8828683PMC
http://dx.doi.org/10.1016/j.stemcr.2021.12.013DOI Listing

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