Accelerated Hematopoietic Stem Cell Aging in Space
Jessica PhamiD, Jane Marie Isquith, Larisa Balaian, Luisa Ladel, Shuvro Prokash NandiiD, Karla Mack, Inge M. van der WerfiD, Emma E. Klacking, Antonio Ruiz, David MaysiD, Paul G. Gamble, Shelby GizaiD, Jiya JanowitziD, Trevor Nienaber, Tejaswini MishraiD, Anna KulidjianiD, Jana StoudemireiD, Michael P. SnyderiD, Twyman ClementsiD, Alysson Renato MuotriiD, Sheldon Morris, Thomas C. WhisenantiD, Ludmil B. AlexandroviD, Catriona H. M. JamiesoniD
Abstract
Stem cell aging is accelerated by macroenvironmental and microenvironmental stressors, including inflammation. Previously, the NASA Twins study revealed inflammatory cytokine upregulation, chromosomal alterations, and telomere changes suggestive of accelerated aging in low-Earth orbit (LEO). To investigate the effects of spaceflight on human hematopoietic stem and progenitor cell (HSPC) aging, the NASA-supported Integrated Space Stem Cell Orbital Research team performed four independent 30- to 45-day NASA missions with matched flight and ground HSPC nanobioreactors in automated CubeLabs. These experiments revealed loss of HSPC dormancy, reduced self-renewal capacity, mitochondrial DNA amplification, APOBEC3-induced C-to-T mutagenesis, reduced ADAR1p150 expression, and alterations in the expression of repetitive elements. These molecular changes are indicative of accelerated HSPC aging and pre-leukemia stem cell generation in space and may be predictable and preventable.
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