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原发性纤毛保护新生小鼠前脑皮质神经元免受环境应激诱导的树突退化。

Primary cilia safeguard cortical neurons in neonatal mouse forebrain from environmental stress-induced dendritic degeneration.

作者信息

Ishii Seiji, Sasaki Toru, Mohammad Shahid, Hwang Hye, Tomy Edwin, Somaa Fahad, Ishibashi Nobuyuki, Okano Hideyuki, Rakic Pasko, Hashimoto-Torii Kazue, Torii Masaaki

机构信息

Center for Neuroscience Research, Children's Research Institute, Children's National Hospital, Washington, DC 20010.

Department of Physiology, Keio University School of Medicine, Tokyo 160-8582, Japan.

出版信息

Proc Natl Acad Sci U S A. 2021 Jan 5;118(1). doi: 10.1073/pnas.2012482118. Epub 2020 Dec 21.

Abstract

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.

摘要

发育中的大脑面临着多种环境应激源的暴露风险。虽然围产期暴露于过量的环境应激会导致一系列神经和精神疾病,但发育中的大脑具备内在的细胞保护机制,其具体机制尚不清楚。在这里,我们以新生小鼠为模型系统,表明初级纤毛,即从神经元细胞体伸出的毛发状突起,在保护未成熟神经元免受环境应激暴露的负面影响方面发挥着重要作用。更具体地说,我们发现初级纤毛通过激活定位于纤毛的胰岛素样生长因子1受体和下游的Akt信号通路,防止树突棘在暴露于酒精和氯胺酮这两种主要细胞应激源时发生退化。我们还发现,该信号通路的激活可抑制应激暴露神经元中Caspase-3的激活以及caspase介导的细胞骨架蛋白的切割/片段化。这些结果表明,初级纤毛在减轻环境应激源(如药物)对围产期大脑发育的不利影响方面发挥着不可或缺的作用。

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