Comparative Transcriptomics Identifies Neuronal and Metabolic Adaptations to Hypergravity and Microgravity in Caenorhabditis elegans

被引:10
|
作者
Willis, Craig R. G. [1 ]
Szewczyk, Nathaniel J. [2 ,3 ,4 ,5 ]
Costes, Sylvain, V [6 ]
Udranszky, Ingrid A. [7 ]
Reinsch, Sigrid S. [6 ]
Etheridge, Timothy [1 ]
Conley, Catharine A. [8 ]
机构
[1] Univ Exeter, Coll Life & Environm Sci, Dept Sport & Hlth Sci, Exeter EX1 2LU, Devon, England
[2] Univ Nottingham, Royal Derby Hosp, MRC ARUK Ctr Musculoskeletal Ageing Res, Sch Med, Derby DE22 3DT, England
[3] Univ Nottingham, Royal Derby Hosp, Biomed Res Ctr, Sch Med,Natl Inst Hlth Res, Derby DE22 3DT, England
[4] Ohio Univ, Ohio Musculoskeletal & Neurol Inst OMNI, Athens, OH 43147 USA
[5] Ohio Univ, Dept Biomed Sci, Athens, OH 43147 USA
[6] NASA Ames Res Ctr, Space Biosci Div, Moffett Field, CA 94035 USA
[7] Lockheed Martin Space Operat, Moffett Field, CA 94035 USA
[8] NASA Ames Res Ctr, Space Sci & Astrobiol Div, Moffett Field, CA 94035 USA
基金
英国生物技术与生命科学研究理事会;
关键词
GENE-EXPRESSION; SPACE-FLIGHT; SPACEFLIGHT; STRESS;
D O I
10.1016/j.isci.2020.101734
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 similar to 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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页数:18
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