TY - JOUR
T1 - Primary cilia safeguard cortical neurons in neonatal mouse forebrain from environmental stress-induced dendritic degeneration
AU - Ishii, Seiji
AU - Sasaki, Toru
AU - Mohammad, Shahid
AU - Hwang, Hye
AU - Tomy, Edwin
AU - Somaa, Fahad
AU - Ishibashi, Nobuyuki
AU - Okano, Hideyuki
AU - Rakic, Pasko
AU - Hashimoto-Torii, Kazue
AU - Torii, Masaaki
N1 - Funding Information:
ACKNOWLEDGMENTS. We thank Hiroki Naito, Aiesha Basha, and Akihiko Nakata for their technical assistance and Stephen Page for critical reading of the manuscript. This study was supported by NIH/National Institute on Alcohol Abuse and Alcoholism/National Institute of Mental Health/National Heart, Lung, and Blood Institute/National Institute on Drug Abuse R01AA025215 (K.H.-T.), R01MH111674 (M.T.), R21AA024882, R01AA026272 (K.H.-T. and M.T.), R01HL139712, R01HL146670 (N.I.), and R01DA023999 (P.R.); the Scott-Gentle Foundation (K.H.-T. and M.T.); JSPS KAKENHI (Grant-in-Aid for Research Activity start-up; 17H06563, Grant-in-Aid for Scientific Research [C]; 19K07829) (S.I.); a grant-in-aid from Keio University Sakaguchi-Memorial Medical Science Fund (S.I.); the Kawano Masanori Memorial Public Interest Incorporated Foundation for Promotion of Pediatrics (S.I.); and internal budgets from Keio University, Osaka University, and the National Institute for Basic Biology, including the Program for the Advancement of Research in Core Projects on Longevity of the Keio University Global Research Institute (H.O.). This study was also supported by the Office of the Assistant Secretary of Defense for Health Affairs through the Peer Reviewed Medical Research Program under Award W81XWH2010199 (N.I.), and by Award 1U54HD090257-01 from the NIH, and the District of Columbia Intellectual and Developmental Disabilities Research Center Award program.
Funding Information:
We thank Hiroki Naito, Aiesha Basha, and Akihiko Nakata for their technical assistance and Stephen Page for critical reading of the manuscript. This study was supported by NIH/National Institute on Alcohol Abuse and Alcoholism/National Institute of Mental Health/National Heart, Lung, and Blood Institute/National Institute on Drug Abuse R01AA025215 (K.H.-T.), R01MH111674 (M.T.), R21AA024882, R01AA026272 (K.H.-T. and M.T.), R01HL139712, R01HL146670 (N.I.), and R01DA023999 (P.R.); the Scott-Gentle Foundation (K.H.-T. and M.T.); JSPS KAKENHI (Grant-in-Aid for Research Activity start-up; 17H06563, Grant-in-Aid for Scientific Research [C]; 19K07829) (S.I.); a grant-in-aid from Keio University Sakaguchi-Memorial Medical Science Fund (S.I.); the Kawano Masanori Memorial Public Interest Incorporated Foundation for Promotion of Pediatrics (S.I.); and internal budgets from Keio University, Osaka University, and the National Institute for Basic Biology, including the Program for the Advancement of Research in Core Projects on Longevity of the Keio University Global Research Institute (H.O.). This study was also supported by the Office of the Assistant Secretary of Defense for Health Affairs through the Peer ReviewedMedical Research Program under AwardW81XWH2010199 (N.I.), and by Award 1U54HD090257-01 from the NIH, and the District of Columbia Intellectual and Developmental Disabilities Research Center Award program.
Publisher Copyright:
© 2021 National Academy of Sciences. All rights reserved.
PY - 2021/1/5
Y1 - 2021/1/5
N2 - The developing brain is under the risk of exposure to a multitude of environmental stressors. While perinatal exposure to excessive levels of environmental stress is responsible for a wide spectrum of neurological and psychiatric conditions, the developing brain is equipped with intrinsic cell protection, the mechanisms of which remain unknown. Here we show, using neonatal mouse as a model system, that primary cilia, hair-like protrusions from the neuronal cell body, play an essential role in protecting immature neurons from the negative impacts of exposure to environmental stress. More specifically, we found that primary cilia prevent the degeneration of dendritic arbors upon exposure to alcohol and ketamine, two major cell stressors, by activating cilia-localized insulin-like growth factor 1 receptor and downstream Akt signaling. We also found that activation of this pathway inhibits Caspase-3 activation and caspase-mediated cleavage/fragmentation of cytoskeletal proteins in stress-exposed neurons. These results indicate that primary cilia play an integral role in mitigating adverse impacts of environmental stressors such as drugs on perinatal brain development.
AB - The developing brain is under the risk of exposure to a multitude of environmental stressors. While perinatal exposure to excessive levels of environmental stress is responsible for a wide spectrum of neurological and psychiatric conditions, the developing brain is equipped with intrinsic cell protection, the mechanisms of which remain unknown. Here we show, using neonatal mouse as a model system, that primary cilia, hair-like protrusions from the neuronal cell body, play an essential role in protecting immature neurons from the negative impacts of exposure to environmental stress. More specifically, we found that primary cilia prevent the degeneration of dendritic arbors upon exposure to alcohol and ketamine, two major cell stressors, by activating cilia-localized insulin-like growth factor 1 receptor and downstream Akt signaling. We also found that activation of this pathway inhibits Caspase-3 activation and caspase-mediated cleavage/fragmentation of cytoskeletal proteins in stress-exposed neurons. These results indicate that primary cilia play an integral role in mitigating adverse impacts of environmental stressors such as drugs on perinatal brain development.
KW - Cortical neurons
KW - Dendrite
KW - Environmental stress
KW - Ketamine
KW - Primary cilia
UR - http://www.scopus.com/inward/record.url?scp=85098179475&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85098179475&partnerID=8YFLogxK
U2 - 10.1073/pnas.2012482118
DO - 10.1073/pnas.2012482118
M3 - Article
C2 - 33443207
AN - SCOPUS:85098179475
SN - 0027-8424
VL - 118
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 1
M1 - e2012482118
ER -