Sechenov Institute of Evolutionary Physiology and Biochemistry of the Russian Academy of Sciences, pr.Torez 44, Saint-Petersburg, Russia.
AIV Institute, University of Eastern Finland, P.O.Box 1627/Neulaniementie 2, 70211, Kuopio, Finland; Laboratory of Neurobiology, Kazan Federal University, Kazan, 420008, Russia.
Biochem Biophys Res Commun. 2018 Nov 30;506(3):648-652. doi: 10.1016/j.bbrc.2018.10.140. Epub 2018 Oct 27.
Homocysteine (HCY) induced neurotoxicity largely depends on interaction of this endogenous amino acid with glutamate NMDA receptors (NMDARs). This receptor type is composed by GluN1 and different GluN2 (A, B, C or D) subunits. However, the receptor activity of HCY in brain regions which differ in relative contribution of GluN2 subunits was not tested so far. In the current study, we explored the action of HCY on cerebellar neurons which natively express GluN2C and GluN2D subunits of NMDARs and compared this with the action of HCY on cortical neurons which are mainly composed by GluN2A and GluN2B subunits. To validate obtained results, we also studied the responses to HCY in recombinant GluN1/2C and GluN1/2D NMDARs expressed in HEK293T cells. Responses to HCY were compared to membrane currents evoked by glutamate or by the specific agonist NMDA. First, we found that on HEK cells expressing GluN1/2C or GluN1/2D NMDARs, HCY was full agonist producing membrane currents similar in amplitude to currents induced by glutamate. The EC values for these particular receptor subtype activation were 80 μM and 31 μM, respectively. Then, we found that HCY similarly to NMDA, evoked large slightly desensitizing membrane currents in native NMDARs of cerebellar and cortical neurons. In cortical neurons, the ratio of the respective currents (I/I) was 0.16 and did not significantly change during in vitro maturation. In sharp contrast, in cerebellar neurons, the ratio of currents evoked by HCY and NMDA was dramatically increased from 0.31 to 0.72 from 7 to 21 day in culture. We show that least 75% of HCY-induced currents in cerebellum were mediated by GluN2C- or GluN2D-containing NMDARs. Thus, our data revealed a large population of cerebellar NMDA receptors highly sensitive to HCY which suggest potential vulnerability of this brain region to pathological conditions associated with enhanced levels of this neurotoxic amino acid.
同型半胱氨酸(HCY)诱导的神经毒性在很大程度上取决于内源性氨基酸与谷氨酸 NMDA 受体(NMDAR)的相互作用。这种受体类型由 GluN1 和不同的 GluN2(A、B、C 或 D)亚基组成。然而,迄今为止,尚未测试 HCY 在相对 GluN2 亚基贡献不同的脑区的受体活性。在本研究中,我们研究了 HCY 对小脑神经元的作用,小脑神经元天然表达 NMDAR 的 GluN2C 和 GluN2D 亚基,并将其与 HCY 对皮质神经元的作用进行了比较,皮质神经元主要由 GluN2A 和 GluN2B 亚基组成。为了验证获得的结果,我们还研究了在 HEK293T 细胞中表达的重组 GluN1/2C 和 GluN1/2D NMDAR 对 HCY 的反应。将对 HCY 的反应与谷氨酸或特定激动剂 NMDA 诱发的膜电流进行了比较。首先,我们发现,在表达 GluN1/2C 或 GluN1/2D NMDAR 的 HEK 细胞上,HCY 是完全激动剂,产生的膜电流幅度与谷氨酸诱导的电流相似。这些特定受体亚型激活的 EC 值分别为 80μM 和 31μM。然后,我们发现 HCY 与 NMDA 相似,在小脑和皮质神经元的天然 NMDAR 中诱发大的、轻微脱敏的膜电流。在皮质神经元中,相应电流的比值(I/I)为 0.16,在体外成熟过程中没有明显变化。相比之下,在小脑神经元中,HCY 和 NMDA 诱发的电流比值从培养的第 7 天到第 21 天从 0.31 急剧增加到 0.72。我们表明,小脑中至少 75%的 HCY 诱导电流是由含有 GluN2C 或 GluN2D 的 NMDAR 介导的。因此,我们的数据揭示了小脑 NMDA 受体对 HCY 高度敏感的大量群体,这表明该脑区可能容易受到与这种神经毒性氨基酸水平升高相关的病理状况的影响。