Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/132882
Title: Exhaustion of mitochondrial and autophagic reserve may contribute to the development of LRRK2 G2019S -Parkinson's disease
Author: Juárez Flores, Diana Luz
González Casacuberta, Ingrid
Ezquerra, Mario
Bañó, María
Carmona Pontaque, Francesc
Catalán García, Marc
Guitart Mampel, Mariona
Rivero, Juan José
Tobias, Ester
Milisenda, Jose Cesar
Tolosa, Eduardo
Martí Domènech, Ma. Josep
Fernández Santiago, Ruben
Cardellach, Francesc
Morén, Constanza
Garrabou Tornos, Glòria
Keywords: Malaltia de Parkinson
Autofàgia
Fibroblasts
Mitocondris
Parkinson's disease
Autophagy
Fibroblasts
Mitochondria
Issue Date: 8-Jun-2018
Publisher: BioMed Central
Abstract: BACKGROUND: Mutations in leucine rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson's disease (PD). Mitochondrial and autophagic dysfunction has been described as etiologic factors in different experimental models of PD. We aimed to study the role of mitochondria and autophagy in LRRK2 G2019S -mutation, and its relationship with the presence of PD-symptoms. METHODS: Fibroblasts from six non-manifesting LRRK2 G2019S -carriers (NM-LRRK2 G2019S ) and seven patients with LRRK2 G2019S -associated PD (PD-LRRK2 G2019S ) were compared to eight healthy controls (C). An exhaustive assessment of mitochondrial performance and autophagy was performed after 24-h exposure to standard (glucose) or mitochondrial-challenging environment (galactose), where mitochondrial and autophagy impairment may be heightened. RESULTS: A similar mitochondrial phenotype of NM-LRRK2 G2019S and controls, except for an early mitochondrial depolarization (54.14% increased, p = 0.04), was shown in glucose. In response to galactose, mitochondrial dynamics of NM-LRRK2 G2019S improved (- 17.54% circularity, p = 0.002 and + 42.53% form factor, p = 0.051), probably to maintain ATP levels over controls. A compromised bioenergetic function was suggested in PD-LRRK2 G2019S when compared to controls in glucose media. An inefficient response to galactose and worsened mitochondrial dynamics (- 37.7% mitochondrial elongation, p = 0.053) was shown, leading to increased oxidative stress. Autophagy initiation (SQTSM/P62) was upregulated in NM-LRRK2 G2019S when compared to controls (glucose + 118.4%, p = 0.014; galactose + 114.44%, p = 0.009,) and autophagosome formation increased in glucose media. Despite of elevated SQSTM1/P62 levels of PD-NM G2019S when compared to controls (glucose + 226.14%, p = 0.04; galactose + 78.5%, p = 0.02), autophagosome formation was deficient in PD-LRRK2 G2019S when compared to NM-LRRK2 G2019S (- 71.26%, p = 0.022). CONCLUSIONS: Enhanced mitochondrial performance of NM-LRRK2 G2019S in mitochondrial-challenging conditions and upregulation of autophagy suggests that an exhaustion of mitochondrial bioenergetic and autophagic reserve, may contribute to the development of PD in LRRK2 G2019S mutation carriers.
Note: Reproducció del document publicat a: https://doi.org/10.1186/s12967-018-1526-3
It is part of: Journal of Translational Medicine, 2018, vol. 16, num. 1, p. 160-173
URI: http://hdl.handle.net/2445/132882
Related resource: https://doi.org/10.1186/s12967-018-1526-3
ISSN: 1479-5876
Appears in Collections:Articles publicats en revistes (Medicina)
Articles publicats en revistes (Genètica, Microbiologia i Estadística)
Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)

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