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在大鼠大脑背侧海马区存在 A2AR-TrkB 异源受体复合物的证据:A2AR 和 TrkB 相互作用对衰老的潜在影响。

Evidence for the existence of A2AR-TrkB heteroreceptor complexes in the dorsal hippocampus of the rat brain: Potential implications of A2AR and TrkB interplay upon ageing.

机构信息

Department of Experimental and Clinical Medicine, Faculty of Medicine and Surgery, Università Politecnica Delle Marche, Ancona, Italy.

Department of Biomolecular Sciences, University of Urbino Carlo Bo, Urbino, Italy.

出版信息

Mech Ageing Dev. 2020 Sep;190:111289. doi: 10.1016/j.mad.2020.111289. Epub 2020 Jun 18.

DOI:10.1016/j.mad.2020.111289
PMID:32565059
Abstract

Adenosine A2A receptors (A2AR) are crucial in facilitating the BDNF action on synaptic transmission in the rat hippocampus primarily upon ageing. Furthermore, it has been suggested that A2AR-Tropomyosin related kinase B receptor (TrkB) crosstalk has a pivotal role in adenosine A2AR-mediated modulation of the BDNF action on hippocampal plasticity. Considering the impact of the above receptors interplay on what concerns BDNF-induced enhancement of synaptic transmission, gaining a better insight into the mechanisms behind this powerful crosstalk becomes of primary interest. Using in situ proximity ligation assay (PLA), the existence of a direct physical interaction between adenosine A2AR and TrkB is demonstrated. The A2AR-TrkB heteroreceptor complexes show a heterogeneous distribution within the rat dorsal hippocampus. High densities of the heteroreceptor complexes were observed in the pyramidal cell layers of CA1-CA3 regions and in the polymorphic layer of the dentate gyrus (DG). The stratum radiatum of the CA1-3 regions showed positive PLA signal in contrast to the oriens region. The molecular and granular layers of the DG also lacked significant densities of PLA positive heteroreceptor complexes, but subgranular zone showed some PLA positive cells. Their allosteric receptor-receptor interactions may significantly modulate BDNF signaling impacting on hippocampal plasticity which is impaired upon ageing.

摘要

腺苷 A2A 受体 (A2AR) 在促进大鼠海马体中 BDNF 对突触传递的作用中至关重要,尤其是在衰老时。此外,有人提出,A2AR-原肌球蛋白相关激酶 B 受体 (TrkB) 串扰在腺苷 A2AR 介导的 BDNF 对海马体可塑性的作用调节中具有关键作用。考虑到上述受体相互作用对 BDNF 诱导的突触传递增强的影响,深入了解这种强大串扰背后的机制变得至关重要。使用原位邻近连接分析 (PLA),证明了腺苷 A2AR 和 TrkB 之间存在直接的物理相互作用。A2AR-TrkB 异源受体复合物在大鼠背侧海马体中呈现出异质分布。在 CA1-CA3 区域的锥体细胞层和齿状回 (DG) 的多形层中观察到异源受体复合物的高密度。CA1-3 区域的放射状层显示出阳性 PLA 信号,而门区则没有。DG 的分子层和颗粒层也缺乏明显密度的 PLA 阳性异源受体复合物,但颗粒下区显示出一些 PLA 阳性细胞。它们的变构受体-受体相互作用可能会显著调节 BDNF 信号转导,从而影响海马体可塑性,而海马体可塑性会随着年龄的增长而受损。

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