Primary cilia safeguard cortical neurons in neonatal mouse forebrain from environmental stress-induced dendritic degeneration.
Animals
Animals, Newborn
/ metabolism
Brain
/ metabolism
Cilia
/ metabolism
Dendrites
/ metabolism
Female
Insulin-Like Growth Factor I
/ metabolism
Mice
/ embryology
Mice, Inbred C57BL
Neural Stem Cells
/ metabolism
Neurons
/ metabolism
Pregnancy
Prenatal Exposure Delayed Effects
Prosencephalon
/ embryology
Proto-Oncogene Proteins c-akt
/ metabolism
Signal Transduction
cortical neurons
dendrite
environmental stress
ketamine
primary cilia
Journal
Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876
Informations de publication
Date de publication:
05 01 2021
05 01 2021
Historique:
entrez:
14
1
2021
pubmed:
15
1
2021
medline:
15
5
2021
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 33443207
pii: 2012482118
doi: 10.1073/pnas.2012482118
pmc: PMC7817201
pii:
doi:
Substances chimiques
Insulin-Like Growth Factor I
67763-96-6
Proto-Oncogene Proteins c-akt
EC 2.7.11.1
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NIMH NIH HHS
ID : R01 MH111674
Pays : United States
Organisme : NIAAA NIH HHS
ID : R21 AA024882
Pays : United States
Organisme : NIDA NIH HHS
ID : R37 DA023999
Pays : United States
Organisme : NIAAA NIH HHS
ID : R01 AA025215
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL146670
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA023999
Pays : United States
Organisme : NICHD NIH HHS
ID : U54 HD090257
Pays : United States
Organisme : NIAAA NIH HHS
ID : R01 AA026272
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL139712
Pays : United States
Déclaration de conflit d'intérêts
Competing interest statement: H.O. is a founding scientist of SanBio Co. Ltd. and K Pharma Inc.
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