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脑兴奋性神经元突触前支架蛋白 Bassoon 介导海马回路成熟:TrkB 信号的潜在参与。

The Presynaptic Scaffold Protein Bassoon in Forebrain Excitatory Neurons Mediates Hippocampal Circuit Maturation: Potential Involvement of TrkB Signalling.

机构信息

Institute of Biology, Otto-Von-Guericke University, 39120 Magdeburg, Germany.

Center for Behavioral Brain Sciences (CBBS), 39120 Magdeburg, Germany.

出版信息

Int J Mol Sci. 2021 Jul 26;22(15):7944. doi: 10.3390/ijms22157944.

Abstract

A presynaptic active zone organizer protein Bassoon orchestrates numerous important functions at the presynaptic active zone. We previously showed that the absence of Bassoon exclusively in forebrain glutamatergic presynapses (cKO) in mice leads to developmental disturbances in dentate gyrus (DG) affecting synaptic excitability, morphology, neurogenesis and related behaviour during adulthood. Here, we demonstrate that hyperexcitability of the medial perforant path-to-DG (MPP-DG) pathway in cKO mice emerges during adolescence and is sustained during adulthood. We further provide evidence for a potential involvement of tropomyosin-related kinase B (TrkB), the high-affinity receptor for brain-derived neurotrophic factor (BDNF), mediated signalling. We detect elevated TrkB protein levels in the dorsal DG of adult mice (3-5 months-old) but not in adolescent (4-5 weeks-old) mice. Electrophysiological analysis reveals increased field-excitatory-postsynaptic-potentials (fEPSPs) in the DG of the adult, but not in adolescent cKO mice. In line with an increased TrkB expression during adulthood in cKO, blockade of TrkB normalizes the increased synaptic excitability in the DG during adulthood, while no such effect was observed in adolescence. Accordingly, neurogenesis, which has previously been found to be increased in adult cKO mice, was unaffected at adolescent age. Our results suggest that Bassoon plays a crucial role in the TrkB-dependent postnatal maturation of the hippocampus.

摘要

一个突触前活性区组织蛋白 Bassoon 在突触前活性区协调着许多重要的功能。我们之前的研究表明,在小鼠中特异性敲除大脑谷氨酸能突触前的 Bassoon(cKO)会导致齿状回(DG)的发育障碍,从而影响成年期的突触兴奋性、形态、神经发生和相关行为。在这里,我们证明了 cKO 小鼠内侧穿通通路到 DG(MPP-DG)途径的过度兴奋在青春期出现,并在成年期持续存在。我们进一步提供了证据表明,原肌球蛋白相关激酶 B(TrkB),脑源性神经营养因子(BDNF)的高亲和力受体,可能参与了信号转导。我们在成年小鼠(约 3-5 个月大)的背侧 DG 中检测到 TrkB 蛋白水平升高,但在青春期(约 4-5 周龄)小鼠中没有检测到。电生理分析显示,成年 cKO 小鼠的 DG 中的场兴奋性突触后电位(fEPSP)增加。与成年 cKO 中 TrkB 表达增加一致,阻断 TrkB 可使 DG 中的突触兴奋性增加正常化,而在青春期则没有观察到这种效应。相应地,先前发现成年 cKO 小鼠中的神经发生增加,但在青春期没有受到影响。我们的结果表明,Bassoon 在海马的 TrkB 依赖性出生后成熟过程中起着至关重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45d2/8347324/a70e2f6ac4e7/ijms-22-07944-g001.jpg

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