
Selective inactivation of leucine-rich repeat kinase 1 and 2 (LRRK1 and LRRK2) in dopaminergic neurons leads to age-dependent loss of midbrain dopaminergic neurons, demonstrating the intrinsic importance of LRRK proteins in the survival of dopaminergic neurons.


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Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common genetic cause of Parkinson’s disease (PD), which is the leading neurodegenerative movement disorder characterized by the progressive loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNpc). However, whether LRRK2 mutations cause PD and degeneration of DA neurons via a toxic gain-of-function or a loss-of-function mechanism is unresolved and has pivotal implications for LRRK2-based PD therapies. In this study, we investigate whether LRRK2 and its functional homologue LRRK1 play an essential, intrinsic role in DA neuron survival through the development of DA neuron-specific LRRK conditional double knockout (cDKO) mice. We first generated and characterized floxed LRRK1 and LRRK2 mice and then confirmed that germline deletions of the floxed LRRK1 and LRRK2 alleles result in null mutations, as evidenced by the absence of LRRK1 and LRRK2 mRNA and protein in the respective homozygous deleted mutant mice. We further examined the specificity of Cre-mediated recombination driven by the dopamine transporter - Cre ( DAT-Cre ) knockin (KI) allele using a GFP reporter line and confirmed that DAT-Cre -mediated recombination is restricted to DA neurons in the SNpc. Crossing these validated floxed LRRK1 and LRRK2 mice with DAT-Cre KI mice, we then generated DA neuron-restricted LRRK cDKO mice and further showed that levels of LRRK1 and LRRK2 are reduced in dissected ventral midbrains of LRRK cDKO mice. While DA neuron-restricted LRRK cDKO mice of both sexes exhibit normal mortality and body weight, they develop age-dependent loss of DA neurons in the SNpc, as demonstrated by the progressive reduction of DA neurons in the SNpc of LRRK cDKO mice at the ages of 20 and 24 months but the unaffected number of DA neurons at the age of 15 months. Moreover, DA neurodegeneration is accompanied with increases of apoptosis and elevated microgliosis in the SNpc as well as decreases of DA terminals in the striatum, and is preceded by impaired motor coordination. Taken together, these findings provide the unequivocal evidence for the importance of LRRK in DA neurons and raise the possibility that LRRK2 mutations may impair its protection of DA neurons, leading to DA neurodegeneration in PD.

### Competing Interest Statement

The authors have declared no competing interest.

All data generated and analyzed in this study are included in the manuscript and the supporting information. Source Data files are provided for key findings shown in [Figures 1][1], 3, 4, 8, and 9.

 [1]: #F1

Cell autonomous role of leucine-rich repeat kinase in protection of dopaminergic neuron survival

selective-inactivation-of-leucine-rich-repeat-kinase-1-and-2-in-dopaminergic-neurons-leads-to-age-dependent-loss-of-midbrain-dopaminergic-neurons


Selective Inactivation of Leucine-Rich Repeat Kinase 1 and 2 in Dopaminergic Neurons Leads to Age-Dependent Loss of Midbrain Dopaminergic Neurons
