Veneto Institute of Molecular Medicine, Via Orus 2, 35129 Padova, Italy.
Padova Neuroscience Center (PNC), Università degli Studi di Padova Via Orus 2, 35129 Padova, Italy.
Cells. 2021 Nov 17;10(11):3212. doi: 10.3390/cells10113212.
The LRRK2 gene is the major genetic determinant of familiar Parkinson's disease (PD). Leucine-rich repeat kinase 2 (LRRK2) is a multidomain protein involved in several intracellular signaling pathways. A wealth of evidence indicates that LRRK2 is enriched at the presynaptic compartment where it regulates vesicle trafficking and neurotransmitter release. However, whether the role of LRRK2 affects neuronal networks dynamic at systems level remains unknown. Addressing this question is critical to unravel the impact of LRRK2 on brain function. Here, combining behavioral tests, electrophysiological recordings, and functional imaging, we investigated neuronal network dynamics, in vivo, in the olfactory bulb of mice carrying a null mutation in LRRK2 gene (LRRK2 knockout, LRRK2 KO, mice). We found that LRRK2 KO mice exhibit olfactory behavioral deficits. At the circuit level, the lack of LRRK2 expression results in altered gamma rhythms and odorant-evoked activity with significant impairments, while the spontaneous activity exhibited limited alterations. Overall, our data in the olfactory bulb suggest that the multifaced role of LRRK2 has a strong impact at system level when the network is engaged in active sensory processing.
LRRK2 基因是家族性帕金森病(PD)的主要遗传决定因素。富含亮氨酸重复激酶 2(LRRK2)是一种参与多种细胞内信号通路的多功能蛋白。大量证据表明,LRRK2 在突触前区富集,在那里它调节囊泡运输和神经递质释放。然而,LRRK2 的作用是否影响系统水平的神经元网络动态尚不清楚。解决这个问题对于揭示 LRRK2 对大脑功能的影响至关重要。在这里,我们结合行为测试、电生理记录和功能成像,研究了携带 LRRK2 基因缺失突变(LRRK2 敲除,LRRK2 KO,小鼠)的小鼠嗅球中的神经元网络动态。我们发现 LRRK2 KO 小鼠表现出嗅觉行为缺陷。在电路水平上,缺乏 LRRK2 表达导致伽马节律和气味诱发活动发生改变,具有显著的损伤,而自发活动表现出有限的改变。总的来说,我们在嗅球中的数据表明,当网络参与主动感觉处理时,LRRK2 的多方面作用对系统水平有很大的影响。