Primary cilia safeguard cortical neurons in neonatal mouse forebrain from environmental stress-induced dendritic degeneration.
Seiji IshiiToru SasakiShahid MohammadHye HwangEdwin TomyFahad SomaaNobuyuki IshibashiHideyuki OkanoPasko RakicKazue Hashimoto-ToriiMasaaki ToriiPublished in: Proceedings of the National Academy of Sciences of the United States of America (2020)
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.
Keyphrases
- stress induced
- single cell
- human health
- spinal cord
- cell therapy
- resting state
- life cycle
- cerebral ischemia
- signaling pathway
- risk assessment
- pregnant women
- stem cells
- functional connectivity
- oxidative stress
- multiple sclerosis
- climate change
- physical activity
- chronic pain
- subarachnoid hemorrhage
- brain injury
- bone marrow
- mesenchymal stem cells
- heat stress
- blood brain barrier
- binding protein
- dna binding