Kim Hyunbin, Park Geunhong, Shin Hyo Geun, Kwon Duwan, Kim Heejung, Baek In-Yeop, Nam Min-Ho, Cho Il-Joo, Kim Jeongjin, Seong Jihye
Brain Science Institute, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.
Department of Pharmacology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
J Neurosci. 2025 Jan 1;45(1):e1473242024. doi: 10.1523/JNEUROSCI.1473-24.2024.
Dopaminergic neurotransmission plays a crucial role in motor function through the coordination of dopamine receptor (DRD) subtypes, such as DRD1 and DRD2, thus the functional imbalance of these receptors can lead to Parkinson's disease. However, due to the complexity of dopaminergic circuits in the brain, it is limited to investigating the individual functions of each DRD subtype in specific brain regions. Here, we developed a light-responsive chimeric DRD2, OptoDRD2, which can selectively activate DRD2-like signaling pathways with spatiotemporal resolution. OptoDRD2 was designed to include the light-sensitive component of rhodopsin and the intracellular signaling domain of DRD2. Upon illumination with blue light, OptoDRD2 triggered DRD2-like signaling pathways, such as Gαi/o subtype recruitment, a decrease in cAMP levels, and ERK phosphorylation. To explore unknown roles of DRD2 in glutamatergic cell populations of basal ganglia circuitry, OptoDRD2 was genetically expressed in excitatory neurons in lateral globus pallidus (LGP) of the male mouse brain. The optogenetic stimulation of OptoDRD2 in the LGP region affected a wide range of locomotion-related parameters, such as increased frequency of movement and decreased immobility time, resulting in the facilitation of motor function of living male mice. Therefore, our findings indicate a potentially novel role for DRD2 in the excitatory neurons of the LGP region, suggesting that OptoDRD2 can be a valuable tool enabling the investigation of unknown roles of DRD2 at specific cell types or brain regions.
多巴胺能神经传递通过协调多巴胺受体(DRD)亚型(如DRD1和DRD2)在运动功能中发挥关键作用,因此这些受体的功能失衡会导致帕金森病。然而,由于大脑中多巴胺能回路的复杂性,研究每个DRD亚型在特定脑区的个体功能受到限制。在此,我们开发了一种光响应嵌合DRD2,即光控DRD2(OptoDRD2),它可以在时空分辨率上选择性激活类似DRD2的信号通路。OptoDRD2被设计为包含视紫红质的光敏成分和DRD2的细胞内信号结构域。在用蓝光照射时,OptoDRD2触发了类似DRD2的信号通路,如Gαi/o亚型募集、cAMP水平降低和ERK磷酸化。为了探索DRD2在基底神经节回路谷氨酸能细胞群体中的未知作用,OptoDRD2在雄性小鼠大脑外侧苍白球(LGP)的兴奋性神经元中进行基因表达。在LGP区域对OptoDRD2进行光遗传学刺激影响了广泛的与运动相关的参数,如运动频率增加和不动时间减少,从而促进了活体雄性小鼠的运动功能。因此,我们的研究结果表明DRD2在LGP区域的兴奋性神经元中具有潜在的新作用,这表明OptoDRD2可以成为一种有价值的工具,用于研究DRD2在特定细胞类型或脑区的未知作用。