4.3 Article

The Roles of Apoptotic Pathways in the Low Recovery Rate After Cryopreservation of Dissociated Human Embryonic Stem Cells

Journal

BIOTECHNOLOGY PROGRESS
Volume 26, Issue 3, Pages 827-837

Publisher

WILEY
DOI: 10.1002/btpr.368

Keywords

cryopreservation of hES cells; apoptosis pathways; reactive oxygen species; F-actin; apoptosis inhibitors

Funding

  1. Biotechnology and Bioengineering Science Research Council (BBSRC) of the UK [BB/D014751/1]
  2. Wellcome trust
  3. John Fell OUP Research Fund
  4. Biotechnology and Biological Sciences Research Council [BB/D014751/1, BB/D014824/1, BBS/B/03599] Funding Source: researchfish
  5. BBSRC [BB/D014824/1, BB/D014751/1] Funding Source: UKRI

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Human embryonic stem (hES) cells have enormous potential for clinical applications. However, one major challenge is to achieve high cell recovery rate after cryopreservation. Understanding how the conventional cryopreservation protocol fails to protect the cells is a prerequisite for developing efficient and successful cryopreservation methods for hES cell lines and banks. We investigated how the stimuli from cryopreservation result in apoptosis, which causes the low cell recovery rate after cryopreservation. The level of reactive oxygen species (ROS) is significantly increased, F-actin content and distribution is altered, and caspase-8 and caspase-9 are activated after cryopreservation. p53 is also activated and translocated into nucleus. During cryopreservation apoptosis is induced by activation of both caspase-8 through the extrinsic pathway and caspase-9 through the intrinsic pathway. However, exactly how the extrinsic pathway is activated is still unclear and deserves further investigation. (C) 2010 American Institute of Chemical Engineers Biotechnol. Prog., 26: 827-837, 2010

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