TY - JOUR
T1 - Artificial gravity partially protects space-induced neurological deficits in Drosophila melanogaster
AU - Mhatre, Siddhita D.
AU - Iyer, Janani
AU - Petereit, Juli
AU - Dolling-Boreham, Roberta M.
AU - Tyryshkina, Anastasia
AU - Paul, Amber M.
AU - Gilbert, Rachel
AU - Jensen, Matthew
AU - Woolsey, Rebekah J.
AU - Anand, Sulekha
AU - Sowa, Marianne B.
AU - Quilici, David R.
AU - Costes, Sylvain V.
AU - Girirajan, Santhosh
AU - Bhattacharya, Sharmila
N1 - Publisher Copyright:
© 2022
PY - 2022/9/6
Y1 - 2022/9/6
N2 - Spaceflight poses risks to the central nervous system (CNS), and understanding neurological responses is important for future missions. We report CNS changes in Drosophila aboard the International Space Station in response to spaceflight microgravity (SFμg) and artificially simulated Earth gravity (SF1g) via inflight centrifugation as a countermeasure. While inflight behavioral analyses of SFμg exhibit increased activity, postflight analysis displays significant climbing defects, highlighting the sensitivity of behavior to altered gravity. Multi-omics analysis shows alterations in metabolic, oxidative stress and synaptic transmission pathways in both SFμg and SF1g; however, neurological changes immediately postflight, including neuronal loss, glial cell count alterations, oxidative damage, and apoptosis, are seen only in SFμg. Additionally, progressive neuronal loss and a glial phenotype in SF1g and SFμg brains, with pronounced phenotypes in SFμg, are seen upon acclimation to Earth conditions. Overall, our results indicate that artificial gravity partially protects the CNS from the adverse effects of spaceflight.
AB - Spaceflight poses risks to the central nervous system (CNS), and understanding neurological responses is important for future missions. We report CNS changes in Drosophila aboard the International Space Station in response to spaceflight microgravity (SFμg) and artificially simulated Earth gravity (SF1g) via inflight centrifugation as a countermeasure. While inflight behavioral analyses of SFμg exhibit increased activity, postflight analysis displays significant climbing defects, highlighting the sensitivity of behavior to altered gravity. Multi-omics analysis shows alterations in metabolic, oxidative stress and synaptic transmission pathways in both SFμg and SF1g; however, neurological changes immediately postflight, including neuronal loss, glial cell count alterations, oxidative damage, and apoptosis, are seen only in SFμg. Additionally, progressive neuronal loss and a glial phenotype in SF1g and SFμg brains, with pronounced phenotypes in SFμg, are seen upon acclimation to Earth conditions. Overall, our results indicate that artificial gravity partially protects the CNS from the adverse effects of spaceflight.
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U2 - 10.1016/j.celrep.2022.111279
DO - 10.1016/j.celrep.2022.111279
M3 - Article
C2 - 36070701
AN - SCOPUS:85137292726
SN - 2211-1247
VL - 40
JO - Cell Reports
JF - Cell Reports
IS - 10
M1 - 111279
ER -