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The Parkinson's disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4

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Item Type:Article
Title:The Parkinson's disease-linked Leucine-rich repeat kinase 2 (LRRK2) is required for insulin-stimulated translocation of GLUT4
Creators Name:Funk, N. and Munz, M. and Ott, T. and Brockmann, K. and Wenninger-Weinzierl, A. and Kühn, R. and Vogt-Weisenhorn, D. and Giesert, F. and Wurst, W. and Gasser, T. and Biskup, S.
Abstract:Mutations within Leucine-rich repeat kinase 2 (LRRK2) are associated with late-onset Parkinson's disease. The physiological function of LRRK2 and molecular mechanism underlying the pathogenic role of LRRK2 mutations remain uncertain. Here, we investigated the role of LRRK2 in intracellular signal transduction. We find that deficiency of Lrrk2 in rodents affects insulin-dependent translocation of glucose transporter type 4 (GLUT4). This deficit is restored during aging by prolonged insulin-dependent activation of protein kinase B (PKB, Akt) and Akt substrate of 160 kDa (AS160), and is compensated by elevated basal expression of GLUT4 on the cell surface. Furthermore, we find a crucial role of Rab10 phosphorylation by LRRK2 for efficient insulin signal transduction. Translating our findings into human cell lines, we find comparable molecular alterations in fibroblasts from Parkinson's patients with the known pathogenic G2019S LRRK2 mutation. Our results highlight the role of LRRK2 in insulin-dependent signalling with potential therapeutic implications.
Keywords:Cell Survival, Fibroblast Growth Factors, Fibroblasts, Glucose Transporter Type 4, Insulin, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Neuronal Outgrowth, Parkinson Disease, Phosphorylation, Proto-Oncogene Proteins c-akt, Signal Transduction, Single Nucleotide Polymorphism, rab GTP-Binding Proteins, Animals, Mice, Rats
Source:Scientific Reports
ISSN:2045-2322
Publisher:Nature Publishing Group
Volume:9
Number:1
Page Range:4515
Date:14 March 2019
Official Publication:https://doi.org/10.1038/s41598-019-40808-y
PubMed:View item in PubMed

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