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Semaphorin 3E 及其受体 PlexinD1 在发育和成年海马形成中的新功能。

New functions of Semaphorin 3E and its receptor PlexinD1 during developing and adult hippocampal formation.

机构信息

Molecular and Cellular Neurobiotechnology, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute of Science and Technology, Parc Científic de Barcelona, Barcelona, Spain.

Department of Cell Biology, Physiology and Immunology, Universitat de Barcelona, Barcelona, Spain.

出版信息

Sci Rep. 2018 Jan 22;8(1):1381. doi: 10.1038/s41598-018-19794-0.

DOI:10.1038/s41598-018-19794-0
PMID:29358640
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5777998/
Abstract

The development and maturation of cortical circuits relies on the coordinated actions of long and short range axonal guidance cues. In this regard, the class 3 semaphorins and their receptors have been seen to be involved in the development and maturation of the hippocampal connections. However, although the role of most of their family members have been described, very few data about the participation of Semaphorin 3E (Sema3E) and its receptor PlexinD1 during the development and maturation of the entorhino-hippocampal (EH) connection are available. In the present study, we focused on determining their roles both during development and in adulthood. We determined a relevant role for Sema3E/PlexinD1 in the layer-specific development of the EH connection. Indeed, mice lacking Sema3E/PlexinD1 signalling showed aberrant layering of entorhinal axons in the hippocampus during embryonic and perinatal stages. In addition, absence of Sema3E/PlexinD1 signalling results in further changes in postnatal and adult hippocampal formation, such as numerous misrouted ectopic mossy fibers. More relevantly, we describe how subgranular cells express PlexinD1 and how the absence of Sema3E induces a dysregulation of the proliferation of dentate gyrus progenitors leading to the presence of ectopic cells in the molecular layer. Lastly, Sema3E mutant mice displayed increased network excitability both in the dentate gyrus and the hippocampus proper.

摘要

皮质回路的发育和成熟依赖于长程和短程轴突导向线索的协调作用。在这方面,已经发现 3 类 semaphorin 及其受体参与了海马连接的发育和成熟。然而,尽管它们的大多数家族成员的作用已经被描述,但是关于 Semaphorin 3E(Sema3E)及其受体 PlexinD1 在神经前体细胞-海马(EH)连接的发育和成熟中的参与的信息非常有限。在本研究中,我们专注于确定它们在发育过程中和成年期的作用。我们确定了 Sema3E/PlexinD1 在 EH 连接的层特异性发育中的重要作用。事实上,缺乏 Sema3E/PlexinD1 信号的小鼠在胚胎和围产期表现出海马中内嗅轴突异常分层。此外,缺乏 Sema3E/PlexinD1 信号导致海马形成的进一步变化,如大量异位苔藓纤维的错误定位。更重要的是,我们描述了颗粒下细胞如何表达 PlexinD1,以及 Sema3E 的缺失如何导致齿状回祖细胞的增殖失调,导致分子层中存在异位细胞。最后,Sema3E 突变小鼠在齿状回和海马体中表现出增强的网络兴奋性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/1e134a9d0f5b/41598_2018_19794_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/04e922f8f6d1/41598_2018_19794_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/a2d6b4668308/41598_2018_19794_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/55d5662630b7/41598_2018_19794_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/32b267c6a222/41598_2018_19794_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/946be8421ef6/41598_2018_19794_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/6c34159e72bc/41598_2018_19794_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/1e134a9d0f5b/41598_2018_19794_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/04e922f8f6d1/41598_2018_19794_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/a2d6b4668308/41598_2018_19794_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/55d5662630b7/41598_2018_19794_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/32b267c6a222/41598_2018_19794_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/946be8421ef6/41598_2018_19794_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/6c34159e72bc/41598_2018_19794_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/5777998/1e134a9d0f5b/41598_2018_19794_Fig7_HTML.jpg

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