LRRK2 Knockout Mice Have an Intact

Hinkle et al. Molecular Neurodegeneration 2012, 7:25 http://www.molecularneurodegeneration.com/content/7/1/25 RESEARCH ARTICLE Open Access LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors Kelly M Hinkle1†, Mei Yue1†, Bahareh Behrouz1, Justus C Dächsel1, Sarah J Lincoln1, Erin E Bowles1, Joel E Beevers1, Brittany Dugger1, Beate Winner2, Iryna Prots2, Caroline B Kent1, Kenya Nishioka1, Wen-Lang Lin1, Dennis W Dickson1, Christopher J Janus3, Matthew J Farrer1,4 and Heather L Melrose1* Abstract Mutations in the LRRK2 gene are the most common cause of genetic Parkinson’s disease. Although the mechanisms behind the pathogenic effects of LRRK2 mutations are still not clear, data emerging from in vitro and in vivo models suggests roles in regulating neuronal polarity, neurotransmission, membrane and cytoskeletal dynamics and protein degradation. We created mice lacking exon 41 that encodes the activation hinge of the kinase domain of LRRK2. We have performed a comprehensive analysis of these mice up to 20 months of age, including evaluation of dopamine storage, release, uptake and synthesis, behavioral testing, dendritic spine and proliferation/neurogenesis analysis. Our results show that the dopaminergic system was not functionally comprised in LRRK2 knockout mice. However, LRRK2 knockout mice displayed abnormal exploratory activity in the open-field test. Moreover, LRRK2 knockout mice stayed longer than their wild type littermates on the accelerated rod during rotarod testing. Finally, we confirm that loss of LRRK2 caused degeneration in the kidney, accompanied by a progressive enhancement of autophagic activity and accumulation of autofluorescent material, but without evidence of biphasic changes. Keywords: Parkinson’s disease, Knockout, Dopamine, Microdialysis, Neuropathology, Open-field, Motor co- ordination, Kidney, Autophagy Background expressing physiological levels of LRRK2 has led to an Mutations in the LRRK2 gene, originally described in 2004, emerging theme that aberrant LRRK2 leads to subtle have now emerged as the most important genetic finding in alterations in dopamine neurotransmission, albeit in the Parkinson’s disease (PD) [1,2]. Incredibly, the most com- absence of dopaminergic neuronal loss [11]. Imaging mon mutation LRRK2 G2019S accounts for up to 40 % of studies in asymptomatic PD patients show the earliest Parkinsonism in populations of certain ethnic descent [3-5]. detectable changes occur in the dopamine transporter LRRK2 mutations also account for around 2% of sporadic and the same holds true for asymptomatic LRRK2 Parkinsonism and two risk factors have been identified in [12,13] and SNCA (alpha-synuclein) patients [14-16]. Asian populations [6-9]. LRRK2-associated PD is a late Neurotransmission alterations in mutant LRRK2 models onset disease and in general the disease resembles idio- may be similar to early preclinical events, suggesting an pathic PD both clinically and pathologically. early involvement in dopamine dysfunction. LRRK2 has been linked to neurite outgrowth, vesicular The expression profile of LRRK2 mRNA suggests that trafficking, protein translation and autophagy [10]. Ana- LRRK2 is unlikely to be an essential developmental pro- lysis of mutant transgenic and knock-in models tein [17]. In adult rodent brain, LRRK2 mRNA is found at highest levels in dopamine receptive areas particularly * Correspondence: [email protected] the striatum [18-22]. However, protein expression of † Equal contributors LRRK2 is abundant throughout the brain including the 1Department of Neuroscience, Mayo Clinic, Jacksonville, Florida 32224, USA Full list of author information is available at the end of the article substantia nigra, striatum, hippocampus, thalamus, © 2012 Hinkle et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Hinkle et al. Molecular Neurodegeneration 2012, 7:25 Page 2 of 17 http://www.molecularneurodegeneration.com/content/7/1/25 cerebellum and cortex [23] suggesting it may have a role the functional integrity of the nigro-striatal dopa- in multiple brain functions (i.e. memory, sensory, emo- minergic pathway. To determine if dopamine neurons or tion) and not just those involved in motor control. their processes were altered in the substantia nigra, we To further study the role of LRRK2 in the brain, we have performed stereological counts of tyrosine hydroxylase developed LRRK2 knockout mice by ablating exon 41 in (TH) positive neurons and dendrites in KO and WT the kinase domain of LRRK2. We have performed a com- mice aged 18–20 months. No differences in neuronal esti- prehensive analysis to study the effect of loss of LRRK2; mates were observed between KO mice (mean estimate ± this includes a thorough investigation of the dopaminergic SEM; 13,766 ± 471) compared to their WT littermates system, extensive behavioral tests to examine motor, co- (12,267 ± 481) (Figure 2A). Similarly, there were no differ- ordination and emotional behavior, as well as neuropatho- ences between dendritic estimates for WT (149,763 ± logical analyses. We find little evidence that loss of LRRK2 6213) and KO (153,873 ± 4351) (Figure 2B). Next, we impacts dopaminergic neurotransmission or striatal beha- examined dopamine axonal neurochemistry by analyzing viors, however we present data showing changes in the ex- total dopamine content in striatal lysates by HPLC from ploratory and motor co-ordination behaviors in these 10 month and 18 month KO mice and WT littermates mice. These findings may be an important consideration (Figure 2C-G, data shown only for 18 months) and found for future anti-LRRK2 therapies. dopamine and its metabolite 3,4-dihydroxyphenylacetic acid (DOPAC), and homovanillic acid (HVA) levels were Results equivalent in KO and WT animals at both time points. Generation of murine LRRK2 knockout mice Since total striatal dopamine includes dopamine that is The targeting strategy for generation of LRRK2 knockout stored, synthesized, released and taken up, we hypothe- (KO) mice is shown in Figure 1A. Homozygous mice sized that we may observe differences in KO mice by received from Ozgene PLC were bred to Jackson C57BL6/ investigating these mechanisms independently. First, we J mice and subsequent heterozygous offspring were bred performed microdialysis to measure extracellular release together to obtain wild type (WT), heterozygous (HET) of dopamine in vivo. Extracellular dopamine levels were and KO animals. Northern blotting analysis with a probe measured before and after KCl-evoked dopamine response designed to LRRK2 exon 24–27 confirmed the absence of in WT, HET and KO mice aged 3–4monthsofage the ~9 kb LRRK2 mRNA transcript in KO mice and a (Figure 2H). Baseline levels of dopamine were not found reduced transcript signal in the HET mice (Figure 1B). to differ between WT (0.13 ± 0.06 pg/μl), HET (0.15 ± Similarly, immunoblotting confirmed absence of LRRK2 0.06 pg/μl) or KO mice (0.16 ± 0.07 pg/μl). When post- protein band in the KO mice and a diminished signal in KCl dopamine levels were normalized to the average of HET mice (Figure 1C). Immunohistochemistry also their individual basal dopamine levels (i.e. % response) no revealed specific signal in the WT compared to KO significant differences were observed (Figure 2I). Next, we (Figure 1D). examined dopamine uptake in the WT, HET and KO mice To determine if any compensatory mRNA changes oc- using a radioactive uptake assay with [3H] dopamine. Up- curred in the paralog LRRK1, we used quantitative Taqman take was comparable across the three groups suggesting a assay with a probe to murine LRRK1 to compare WT, HET functionally intact dopamine transporter (Additional file and KO mice. No significant alterations in LRRK1 mRNA 2: Figure S2A). Concluding that release, storage and up- levels were observed in any of the brain regions tested. We take of dopamine appear to be normal, we then examined also checked mRNA levels of SNCA, MAPT or PARKIN D2-autoreceptor mediated synthesis and release, which is and found no differences (Additional file 1: Figure S1). one of the feedback mechanisms in the striatum. It is well LRRK2 KO mice were fertile and appeared to be healthy known that antagonizing pre-synaptic D2 autoreceptors from birth, with body weights comparable to WT litter- can remove this feedback inhibition and cause increased mates within the study period. HET x HET breedings synthesis as well as release of dopamine [24]. WT, HET yielded Mendelian ratios in line with expected inheritance and KO mice were treated with the D2 receptor antagon- (fromover70litters24.4%WT,51.6%HET,24%KO). ist raclopride, sacrificed 30 min later and HPLC analysis Subsequent characterization experiments were performed performed to quantify dopamine and metabolites. As to compare KO and WT mice at different aging time expected, dopamine turnover, as measured by the ratio of points. Due to animal costs and space restraints, we dopamine metabolites to stores of dopamine increased included a HET group in some, but not all, of these dramatically [One way ANOVA ps < 0.0001 for DOPAC/ analyses. dopamine and HVA/dopamine] following treatment with raclopride (Additional file 2: Figure S2B, C). However, Dopaminergic system characterization Tukey’s post hoc comparisons did not reveal differences in LRRK2 expression is normally found in high levels in the this response between WT, HET or KO mice, suggesting striatum so we reasoned that loss of LRRK2 may impact that autoreceptor-mediated feedback is normal in the Hinkle et al. Molecular Neurodegeneration 2012, 7:25 Page 3 of 17 http://www.molecularneurodegeneration.com/content/7/1/25 Figure 1 Generation and expression characterization of LRRK2 KO mice. (a) Schematic diagram (courtesy of Ozgene PLC) showing targeted locus. Exon 41 was flanked with LoxP sites to allow deletion with Cre recombinase. PKG-Neo-pA-SD-IS is Ozgene’s standard selection cassette and was inserted downstream of exon 41.

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