AI Article Synopsis

  • The LRRK2 gene is crucial for understanding familial Parkinson's disease as it is the major genetic factor associated with the condition.
  • LRRK2 is involved in various cellular signaling pathways and is primarily found in the presynaptic compartment, where it plays a role in managing vesicle trafficking and neurotransmitter release.
  • Research using LRRK2 knockout mice revealed that the absence of LRRK2 leads to significant deficits in olfactory behavior and alters critical neuronal network dynamics, particularly affecting gamma rhythms and response to odors during active sensory processing.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622670PMC
http://dx.doi.org/10.3390/cells10113212DOI Listing

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