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Identification of a fundamental cryoinjury mechanism in MSCs and its mitigation through cell-cycle synchronization prior to freezing.
Johnstone, Brian H; Gu, Dongsheng; Lin, Chieh-Han; Du, Jianguang; Woods, Erik J.
Afiliação
  • Johnstone BH; Ossium Health, Inc., Indianapolis, IN, United States.
  • Gu D; Ossium Health, Inc., Indianapolis, IN, United States.
  • Lin CH; Ossium Health, Inc., Indianapolis, IN, United States.
  • Du J; Ossium Health, Inc., Indianapolis, IN, United States.
  • Woods EJ; Ossium Health, Inc., Indianapolis, IN, United States. Electronic address: erik@ossiumhealth.com.
Cryobiology ; 113: 104592, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37827209
ABSTRACT
Clinical development of cellular therapies, including mesenchymal stem/stromal cell (MSC) treatments, has been hindered by ineffective cryopreservation methods that result in substantial loss of post-thaw cell viability and function. Proposed solutions to generate high potency MSC for clinical testing include priming cells with potent cytokines such as interferon gamma (IFNγ) prior to cryopreservation, which has been shown to enhance post-thaw function, or briefly culturing to allow recovery from cryopreservation injury prior to administering to patients. However, both solutions have disadvantages cryorecovery increases the complexity of manufacturing and distribution logistics, while the pleiotropic effects of IFNγ may have uncharacterized and unintended consequences on MSC function. To determine specific cellular functions impacted by cryoinjury, we first evaluated cell cycle status. It was discovered that S phase MSC are exquisitely sensitive to cryoinjury, demonstrating heightened levels of delayed apoptosis post-thaw and reduced immunomodulatory function. Blocking cell cycle progression at G0/G1 by growth factor deprivation (commonly known as serum starvation) greatly reduced post-thaw dysfunction of MSC by preventing apoptosis induced by double-stranded breaks in labile replicating DNA that form during the cryopreservation and thawing processes. Viability, clonal growth and T cell suppression function were preserved at pre-cryopreservation levels and were no different than cells prior to freezing or frozen after priming with IFNγ. Thus, we have developed a robust and effective strategy to enhance post-thaw recovery of therapeutic MSC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Criopreservação Limite: Humans Idioma: En Revista: Cryobiology Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Criopreservação Limite: Humans Idioma: En Revista: Cryobiology Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos