Microgravity induces proteomics changes involved in endoplasmic reticulum stress and mitochondrial protection.

Journal Article (Journal Article)

On Earth, biological systems have evolved in response to environmental stressors, interactions dictated by physical forces that include gravity. The absence of gravity is an extreme stressor and the impact of its absence on biological systems is ill-defined. Astronauts who have spent extended time under conditions of minimal gravity (microgravity) experience an array of biological alterations, including perturbations in cardiovascular function. We hypothesized that physiological perturbations in cardiac function in microgravity may be a consequence of alterations in molecular and organellar dynamics within the cellular milieu of cardiomyocytes. We used a combination of mass spectrometry-based approaches to compare the relative abundance and turnover rates of 848 and 196 proteins, respectively, in rat neonatal cardiomyocytes exposed to simulated microgravity or normal gravity. Gene functional enrichment analysis of these data suggested that the protein content and function of the mitochondria, ribosomes, and endoplasmic reticulum were differentially modulated in microgravity. We confirmed experimentally that in microgravity protein synthesis was decreased while apoptosis, cell viability, and protein degradation were largely unaffected. These data support our conclusion that in microgravity cardiomyocytes attempt to maintain mitochondrial homeostasis at the expense of protein synthesis. The overall response to this stress may culminate in cardiac muscle atrophy.

Full Text

Duke Authors

Cited Authors

  • Feger, BJ; Thompson, JW; Dubois, LG; Kommaddi, RP; Foster, MW; Mishra, R; Shenoy, SK; Shibata, Y; Kidane, YH; Moseley, MA; Carnell, LS; Bowles, DE

Published Date

  • September 27, 2016

Published In

Volume / Issue

  • 6 /

Start / End Page

  • 34091 -

PubMed ID

  • 27670941

Pubmed Central ID

  • PMC5037457

Electronic International Standard Serial Number (EISSN)

  • 2045-2322

Digital Object Identifier (DOI)

  • 10.1038/srep34091


  • eng

Conference Location

  • England