2022
DOI: 10.1016/j.tins.2021.12.002
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LRRK2 and idiopathic Parkinson’s disease

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Cited by 85 publications
(75 citation statements)
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References 108 publications
(144 reference statements)
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“…Given our findings that (i) LRRK2 is activated in nigral neurons in iPD ( Di Maio et al, 2018 ), NOX2 activity is required for wildtype LRRK2 activation in vivo , and (iii) NOX2 is activated in nigral neurons in iPD, it appears likely this mechanism is operative in the human disease. Endolysosomal deficits and autophagic dysfunction contribute to the progression of PD ( Rocha et al, 2020 ; Rocha et al, 2022 ). Interestingly, aberrant LRRK2 kinase activity has been shown to lead to autophagic dysfunction and endolysosomal deficits with the consequence of accumulation of α-synuclein ( Di Maio et al, 2018 ; Rocha et al, 2020 ; Rocha et al, 2022 ).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Given our findings that (i) LRRK2 is activated in nigral neurons in iPD ( Di Maio et al, 2018 ), NOX2 activity is required for wildtype LRRK2 activation in vivo , and (iii) NOX2 is activated in nigral neurons in iPD, it appears likely this mechanism is operative in the human disease. Endolysosomal deficits and autophagic dysfunction contribute to the progression of PD ( Rocha et al, 2020 ; Rocha et al, 2022 ). Interestingly, aberrant LRRK2 kinase activity has been shown to lead to autophagic dysfunction and endolysosomal deficits with the consequence of accumulation of α-synuclein ( Di Maio et al, 2018 ; Rocha et al, 2020 ; Rocha et al, 2022 ).…”
Section: Discussionmentioning
confidence: 99%
“…Endolysosomal deficits and autophagic dysfunction contribute to the progression of PD ( Rocha et al, 2020 ; Rocha et al, 2022 ). Interestingly, aberrant LRRK2 kinase activity has been shown to lead to autophagic dysfunction and endolysosomal deficits with the consequence of accumulation of α-synuclein ( Di Maio et al, 2018 ; Rocha et al, 2020 ; Rocha et al, 2022 ). Treatment with a LRRK2 kinase inhibitor prevented these deficits in the rotenone rat model (50), suggesting that elevated kinase activity contributes to this process ( Graphical Abstract ).…”
Section: Discussionmentioning
confidence: 99%
“…The functions of LRRK2 are not fully understood, but it has become clear that LRRK2 can trigger autophosphorylation at Ser1292 and phosphorylate a subset of Rab small GTPases (Rab8A and Rab10) (Rocha et al, 2022; Sheng et al, 2012; Steger et al, 2016). A direct readout of these targets was not present in our panel of stains.…”
Section: Discussionmentioning
confidence: 99%
“…Currently, delivering LRRK2 kinase inhibitors such as DNL151 has become an important avenue for treating LRRK2 diseased patients ( Ding and Ren, 2020 ). Mutations in LRRK2 are a relatively common cause of familial late-onset PD, and also linked to the more numerous sporadic PD, suggesting that understanding LRRK2-associated mechanisms might be a gateway to exploring sporadic PD ( Rocha et al, 2022 ). Notably, the multi-domain structure of LRRK2 renders its versatile functions in multiple physiological processes, including migration, autophagy, phagocytosis, and mitochondrial function, among others.…”
Section: Introductionmentioning
confidence: 99%