参与腺苷A受体和A受体诱导神经母细胞瘤细胞及纹状体原代培养物中神经元分化的分子机制。

Molecular mechanisms involved in the adenosine A and A receptor-induced neuronal differentiation in neuroblastoma cells and striatal primary cultures.

作者信息

Canals Meritxell, Angulo Ester, Casadó Vicent, Canela Enric I, Mallol Josefa, Viñals Francesc, Staines William, Tinner Barbro, Hillion Joelle, Agnati Luigi, Fuxe Kjell, Ferré Sergi, Lluis Carmen, Franco Rafael

机构信息

Department de Bioquimica i Biologia Molecular, University of Barcelona, Barcelona, Spain.

出版信息

J Neurochem. 2005 Jan;92(2):337-48. doi: 10.1111/j.1471-4159.2004.02856.x.

Abstract

Adenosine A1 receptors (A1Rs) and adenosine A(2A) receptors (A(2A)Rs) are the major mediators of the neuromodulatory actions of adenosine in the brain. In the striatum A1Rs and A(2A)Rs are mainly co-localized in the GABAergic striatopallidal neurons. In this paper we show that agonist-induced stimulation of A1Rs and A(2A)Rs induces neurite outgrowth processes in the human neuroblastoma cell line SH-SY5Y and also in primary cultures of striatal neuronal precursor cells. The kinetics of adenosine-mediated neuritogenesis was faster than that triggered by retinoic acid. The triggering of the expression of TrkB neurotrophin receptor and the increase of cell number in the G1 phase by the activation of adenosine receptors suggest that adenosine may participate in early steps of neuronal differentiation. Furthermore, protein kinase C (PKC) and extracellular regulated kinase-1/2 (ERK-1/2) are involved in the A1R- and A(2A)R-mediated effects. Inhibition of protein kinase A (PKA) activity results in a total inhibition of neurite outgrowth induced by A(2A)R agonists but not by A1R agonists. PKA activation is therefore necessary for A(2A)R-mediated neuritogenesis. Co-stimulation does not lead to synergistic effects thus indicating that the neuritogenic effects of adenosine are mediated by either A1 or A(2A) receptors depending upon the concentration of the nucleoside. These results are relevant to understand the mechanisms by which adenosine receptors modulate neuronal differentiation and open new perspectives for considering the use of adenosine agonists as therapeutic agents in diseases requiring neuronal repair.

摘要

腺苷A1受体(A1Rs)和腺苷A2A受体(A2ARs)是大脑中腺苷神经调节作用的主要介质。在纹状体中,A1Rs和A2ARs主要共定位于γ-氨基丁酸能纹状体苍白球神经元中。在本文中,我们表明激动剂诱导的A1Rs和A2ARs刺激可诱导人神经母细胞瘤细胞系SH-SY5Y以及纹状体神经元前体细胞原代培养物中的神经突生长过程。腺苷介导的神经突生成动力学比视黄酸触发的动力学更快。腺苷受体激活引发TrkB神经营养因子受体表达以及G1期细胞数量增加,这表明腺苷可能参与神经元分化的早期步骤。此外,蛋白激酶C(PKC)和细胞外调节激酶-1/2(ERK-1/2)参与A1R和A2AR介导的效应。抑制蛋白激酶A(PKA)活性会导致A2AR激动剂诱导的神经突生长完全受到抑制,但A1R激动剂诱导的神经突生长不受影响。因此,PKA激活对于A2AR介导的神经突生成是必要的。共同刺激不会产生协同效应,这表明腺苷的神经突生成效应取决于核苷浓度,由A1或A2A受体介导。这些结果对于理解腺苷受体调节神经元分化的机制具有重要意义,并为考虑将腺苷激动剂用作需要神经元修复的疾病的治疗药物开辟了新的前景。

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