Serrano-Regal Mari Paz, Luengas-Escuza Irene, Bayón-Cordero Laura, Ibarra-Aizpurua Naroa, Alberdi Elena, Pérez-Samartín Alberto, Matute Carlos, Sánchez-Gómez María Victoria
Deparment of Neurosciences, University of the Basque Country (UPV/EHU), Leioa, Spain; Achucarro Basque Center for Neuroscience, Leioa, Spain; Centro de Investigación en Red de Enfermedades Neurodegenerativas (CIBERNED), Leioa, Spain.
Deparment of Neurosciences, University of the Basque Country (UPV/EHU), Leioa, Spain.
Neuroscience. 2020 Jul 15;439:163-180. doi: 10.1016/j.neuroscience.2019.07.014. Epub 2019 Jul 23.
Differentiation of oligodendrocyte precursor cells (OPCs) into mature oligodendrocytes (OLs) is a key event for axonal myelination in the central nervous system (CNS). Several growth factors and neurotransmitters like GABA are postulated as important regulators of that process, and different protein kinases may also participate in OL differentiation and myelination. However, the molecular mechanisms underlying the regulation of myelination by neurotransmitters are only partially known. In the present study, we provide evidence showing that GABA receptors (GABARs) play an important role in OL differentiation. First, we observed that OPCs and OLs synthesize GABA and expressed GABAR and transporters, both in vitro and in vivo and, in contrast to GABARs, the subunits GABAR and GABAR are expressed in OLs over time. Then, we found that exogenous GABA increases the number of myelin segments and MBP expression in DRG-OPC cocultures, indicating that GABA regulates myelination when OLs are in contact with axons. Notably, in purified rat OPC cultures, chronic treatment with GABA and baclofen, specific GABAR agonist, accelerates OPC differentiation by enhancing the processes branching and myelin protein expression, effects that are reverted in presence of GABAR specific antagonist CGP55845. Exposure of OPCs to baclofen promotes the Src-phosphorylation, and the baclofen-induced maturation is attenuated in presence of the Src-family kinases inhibitor PP2. None of these effects are mediated by the GABAR agonist muscimol. Together, these results highlight the relevance of the GABAergic system in OL differentiation, and indicate that this functional role is mediated through GABAR involving the participation of Src-family kinases. This article is part of a Special Issue entitled: Honoring Ricardo Miledi - outstanding neuroscientist of XX-XXI centuries.
少突胶质前体细胞(OPCs)分化为成熟少突胶质细胞(OLs)是中枢神经系统(CNS)轴突髓鞘形成的关键事件。几种生长因子和神经递质如γ-氨基丁酸(GABA)被认为是该过程的重要调节因子,不同的蛋白激酶也可能参与OL分化和髓鞘形成。然而,神经递质调节髓鞘形成的分子机制仅部分为人所知。在本研究中,我们提供证据表明GABA受体(GABARs)在OL分化中起重要作用。首先,我们观察到OPCs和OLs在体外和体内均能合成GABA并表达GABAR和转运体,与GABARs不同,GABAR和GABAR亚基随时间在OLs中表达。然后,我们发现外源性GABA增加了背根神经节-OPC共培养物中髓鞘节段的数量和髓鞘碱性蛋白(MBP)的表达,表明当OLs与轴突接触时GABA调节髓鞘形成。值得注意的是,在纯化的大鼠OPC培养物中,用GABA和巴氯芬(一种特异性GABAR激动剂)进行慢性处理,通过增强突起分支和髓鞘蛋白表达来加速OPC分化,在存在GABAR特异性拮抗剂CGP55845时这些作用会逆转。将OPCs暴露于巴氯芬可促进Src磷酸化,并且在存在Src家族激酶抑制剂PP2时巴氯芬诱导的成熟会减弱。这些效应均不是由GABAR激动剂蝇蕈醇介导的。总之,这些结果突出了GABA能系统在OL分化中的相关性,并表明这种功能作用是通过涉及Src家族激酶参与的GABAR介导的。本文是名为:纪念里卡多·米莱迪——二十世纪至二十一世纪杰出神经科学家的特刊的一部分。