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Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans.
Willis, Craig R G; Szewczyk, Nathaniel J; Costes, Sylvain V; Udranszky, Ingrid A; Reinsch, Sigrid S; Etheridge, Timothy; Conley, Catharine A.
Afiliação
  • Willis CRG; Department of Sport and Health Sciences, College of Life and Environmental Sciences, University of Exeter, Exeter, EX1 2LU, UK.
  • Szewczyk NJ; MRC-ARUK Centre for Musculoskeletal Ageing Research and National Institute of Health Research, Biomedical Research Centre, School of Medicine, Royal Derby Hospital, University of Nottingham, Derby, DE22 3DT, UK.
  • Costes SV; Ohio Musculoskeletal and Neurological Institute (OMNI) and Department of Biomedical Sciences, Ohio University, Athens, OH 43147, USA.
  • Udranszky IA; Space Biosciences Division, NASA Ames Research Center, Moffett Field, CA 94035, USA.
  • Reinsch SS; Lockheed Martin Space Operations, Moffett Field, CA 94035, USA.
  • Etheridge T; Space Biosciences Division, NASA Ames Research Center, Moffett Field, CA 94035, USA.
  • Conley CA; Department of Sport and Health Sciences, College of Life and Environmental Sciences, University of Exeter, Exeter, EX1 2LU, UK.
iScience ; 23(12): 101734, 2020 Dec 18.
Article em En | MEDLINE | ID: mdl-33376968
ABSTRACT
Deep space exploration is firmly within reach, but health decline during extended spaceflight remains a key challenge. In this study, we performed comparative transcriptomic analysis of Caenorhabditis elegans responses to varying degrees of hypergravity and to two spaceflight experiments (ICE-FIRST and CERISE). We found that progressive hypergravitational load concomitantly increases the extent of differential gene regulation and that subtle changes in ∼1,000 genes are reproducibly observed during spaceflight-induced microgravity. Consequently, we deduce those genes that are concordantly regulated by altered gravity per se or that display inverted expression profiles during hypergravity versus microgravity. Through doing so, we identify several candidate targets with terrestrial roles in neuronal function and/or cellular metabolism, which are linked to regulation by daf-16/FOXO signaling. These data offer a strong foundation from which to expedite mechanistic understanding of spaceflight-induced maladaptation in higher organisms and, ultimately, promote future targeted therapeutic development.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article