[HTML][HTML] LRRK2 kinase activity regulates lysosomal glucocerebrosidase in neurons derived from Parkinson's disease patients

D Ysselstein, M Nguyen, TJ Young, A Severino… - Nature …, 2019 - nature.com
D Ysselstein, M Nguyen, TJ Young, A Severino, M Schwake, K Merchant, D Krainc
Nature communications, 2019nature.com
Mutations in LRRK2 and GBA1 are common genetic risk factors for Parkinson's disease (PD)
and major efforts are underway to develop new therapeutics that target LRRK2 or
glucocerebrosidase (GCase). Here we describe a mechanistic and therapeutic convergence
of LRRK2 and GCase in neurons derived from patients with PD. We find that GCase activity
was reduced in dopaminergic (DA) neurons derived from PD patients with LRRK2
mutations. Inhibition of LRRK2 kinase activity results in increased GCase activity in DA …
Abstract
Mutations in LRRK2 and GBA1 are common genetic risk factors for Parkinson’s disease (PD) and major efforts are underway to develop new therapeutics that target LRRK2 or glucocerebrosidase (GCase). Here we describe a mechanistic and therapeutic convergence of LRRK2 and GCase in neurons derived from patients with PD. We find that GCase activity was reduced in dopaminergic (DA) neurons derived from PD patients with LRRK2 mutations. Inhibition of LRRK2 kinase activity results in increased GCase activity in DA neurons with either LRRK2 or GBA1 mutations. This increase is sufficient to partially rescue accumulation of oxidized dopamine and alpha-synuclein in PD patient neurons. We have identified the LRRK2 substrate Rab10 as a key mediator of LRRK2 regulation of GCase activity. Together, these results suggest an important role of mutant LRRK2 as a negative regulator of lysosomal GCase activity.
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