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Swiprosin-1/Efhd2 对成年海马神经发生的影响。

Impact of Swiprosin-1/Efhd2 on Adult Hippocampal Neurogenesis.

机构信息

Department of Stem Cell Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Glueckstrasse 6, Erlangen 91054, Germany; Department of Neurology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany; IZKF Junior Research Group III and BMBF Research Group Neuroscience, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany.

Department of Stem Cell Biology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Glueckstrasse 6, Erlangen 91054, Germany; IZKF Junior Research Group III and BMBF Research Group Neuroscience, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen 91054, Germany.

出版信息

Stem Cell Reports. 2018 Feb 13;10(2):347-355. doi: 10.1016/j.stemcr.2017.12.010. Epub 2018 Jan 11.

Abstract

Swiprosin-1/Efhd2 (Efhd2) is highly expressed in the CNS during development and in the adult. EFHD2 is regulated by Ca binding, stabilizes F-actin, and promotes neurite extension. Previous studies indicated a dysregulation of EFHD2 in human Alzheimer's disease brains. We hypothesized a detrimental effect of genetic ablation of Efhd2 on hippocampal integrity and specifically investigated adult hippocampal neurogenesis. Efhd2 was expressed throughout adult neuronal development and in mature neurons. We observed a severe reduction of the survival of adult newborn neurons in Efhd2 knockouts, starting at the early neuroblast stage. Spine formation and dendrite growth of newborn neurons were compromised in full Efhd2 knockouts, but not upon cell-autonomous Efhd2 deletion. Together with our finding of severe hippocampal tauopathy in Efhd2 knockout mice, these data connect Efhd2 to impaired synaptic plasticity as present in Alzheimer's disease and identify a role of Efhd2 in neuronal survival and synaptic integration in the adult hippocampus.

摘要

Swiprosin-1/Efhd2(Efhd2)在发育过程中和成年期的中枢神经系统中高度表达。EFHD2 受 Ca 结合调节,稳定 F-肌动蛋白,并促进轴突延伸。先前的研究表明 EFHD2 在人类阿尔茨海默病大脑中失调。我们假设 Efhd2 的基因缺失对海马完整性有不利影响,并特别研究了成年海马神经发生。Efhd2 在整个成年神经元发育过程中和成熟神经元中表达。我们观察到 Efhd2 敲除小鼠的成年新生神经元存活率严重降低,从早期神经母细胞阶段开始。新生神经元的棘形成和树突生长在全 Efhd2 敲除小鼠中受损,但在细胞自主 Efhd2 缺失时没有受损。结合我们在 Efhd2 敲除小鼠中发现的严重海马 tau 病,这些数据将 Efhd2 与阿尔茨海默病中存在的受损突触可塑性联系起来,并确定了 Efhd2 在成年海马体中神经元存活和突触整合中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc24/5830914/80f614ad1ba5/gr1.jpg

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