Axonal Lysosomal Assays for Characterizing the Effects of LRRK2 G2019S

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

Abstract

The degeneration of axon terminals before the soma, referred to as "dying back", is a feature of Parkinson's disease (PD). Axonal assays are needed to model early PD pathogenesis as well as identify protective therapeutics. We hypothesized that defects in axon lysosomal trafficking as well as injury repair might be important contributing factors to "dying back" pathology in PD. Since primary human PD neurons are inaccessible, we developed assays to quantify axonal trafficking and injury repair using induced pluripotent stem cell (iPSC)-derived neurons with LRRK2 G2019S, which is one of the most common known PD mutations, and isogenic controls. We observed a subtle axonal trafficking phenotype that was partially rescued by a LRRK2 inhibitor. Mutant LRRK2 neurons showed increased phosphorylated Rab10-positive lysosomes, and lysosomal membrane damage increased LRRK2-dependent Rab10 phosphorylation. Neurons with mutant LRRK2 showed a transient increase in lysosomes at axotomy injury sites. This was a pilot study that used two patient-derived lines to develop its methodology; we observed subtle phenotypes that might correlate with heterogeneity in LRRK2-PD patients. Further analysis using additional iPSC lines is needed. Therefore, our axonal lysosomal assays can potentially be used to characterize early PD pathogenesis and test possible therapeutics.

Details

OriginalspracheEnglisch
Aufsatznummer58
Seitenumfang25
FachzeitschriftBiology
Jahrgang13 (2024)
Ausgabenummer1
PublikationsstatusVeröffentlicht - 20 Jan. 2024
Peer-Review-StatusJa

Externe IDs

ORCID /0000-0002-2387-526X/work/155839604
PubMed 38275734
Mendeley 9666bd95-8ffe-393e-9760-dee335cb2a34
unpaywall 10.3390/biology13010058
Scopus 85190126532

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