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Assaying the Kinase Activity of LRRK2 in vitro
Published on: January 18, 2012
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LRRK2 knockdown in zebrafish causes developmental defects, neuronal loss, and synuclein aggregation.
Shubhangi Prabhudesai1, Fatima Zahra Bensabeur1, Rashed Abdullah1
1Department of Biological Sciences, St. John's University, Queens, New York.
Journal of Neuroscience Research
|June 7, 2016
Summary
Reducing leucine-rich repeat kinase 2 (LRRK2) in zebrafish caused neuronal loss and developmental issues. This suggests LRRK2 is vital for brain and kidney function, impacting Parkinson's disease research.
Area of Science:
- Neuroscience
- Developmental Biology
- Genetics
Background:
- Mutations in leucine-rich repeat kinase 2 (LRRK2) are a common genetic cause of Parkinson's disease.
- The precise function of LRRK2, particularly in neurodevelopment and peripheral organs, remains largely uncharacterized.
- Previous studies in zebrafish yielded conflicting results regarding LRRK2's role in dopaminergic neurons and locomotion.
Purpose of the Study:
- To investigate the functional roles of LRRK2 in zebrafish development and neuronal integrity.
- To explore the impact of LRRK2 knockdown on dopaminergic neurons and associated developmental processes.
- To determine the expression patterns of endogenous LRRK2 in various zebrafish tissues.
Main Methods:
- Utilized morpholino-based knockdown to reduce LRRK2 expression by approximately 50% in zebrafish embryos.
- Assessed developmental phenotypes including axis curvature, ocular abnormalities, and edema.
- Quantified neuronal loss, specifically dopaminergic neurons, using immunofluorescence.
- Examined the expression of β-synuclein, PARK13, and SOD1, and assessed protein localization of Na(+) /K(+) ATPase.
Main Results:
- LRRK2 knockdown led to significant neuronal loss, including dopaminergic neurons, and developmental defects like axis curvature and edema.
- Endogenous LRRK2 expression was detected in the brain, spinal cord, heart, kidney (pronephros), and lens.
- LRRK2 knockdown resulted in the upregulation of β-synuclein, PARK13, and SOD1, with β-synuclein aggregation observed in multiple brain regions.
- Mislocalization of Na(+) /K(+) ATPase in pronephric ducts suggested renal malfunction and a potential role for LRRK2 in kidney development.
Conclusions:
- LRRK2 plays multifaceted roles in zebrafish, influencing both neuronal development and peripheral organ function.
- Zebrafish serve as a valuable model for studying LRRK2's complex functions and its implications in Parkinson's disease.
- LRRK2 is implicated in pronephric duct epithelial cell differentiation and renal function, potentially linking kidney malfunction to observed edema.
