GRK2‐Targeted Knockdown as Therapy for Multiple System Atrophy

Author:

Lopez‐Cuina Miguel1234,Guérin Paul12,Dutheil Nathalie12,Martin Christelle5,Lasserre Thierry Leste6,Fernagut Pierre‐Olivier7ORCID,Meissner Wassilios G.1289ORCID,Bezard Erwan12ORCID

Affiliation:

1. Univ. de Bordeaux, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux France

2. CNRS, Institut des Maladies Neurodégénératives, UMR 5293 Bordeaux France

3. Neurology Department Hospital Universitario Reina Sofía Córdoba Spain

4. Instituto Maimónides de Investigación Biomédica de Córdoba (IMIBIC) Córdoba Spain

5. Univ. de Bordeaux, Interdisciplinary Institute for Neuroscience, UMR 5297 Bordeaux France

6. Univ. Bordeaux, INSERM, PUMA, Neurocentre Magendie, U1215 Bordeaux France

7. Université de Poitiers, Laboratoire de Neurosciences Expérimentales et Cliniques, INSERM UMR_S 1084 Poitiers France

8. CHU Bordeaux, Service de Neurologie des Maladies Neurodégénératives, IMNc Bordeaux France

9. Department of Medicine University of Otago, Christchurch, and New Zealand Brain Research Institute Christchurch New Zealand

Abstract

AbstractBackgroundMultiple system atrophy (MSA) is a sporadic adult‐onset rare neurodegenerative synucleinopathy for which counteracting central nervous system insulin resistance bears the potential of being neuroprotective. G‐protein‐(heterotrimeric guanine nucleotide‐binding protein)‐coupled receptor kinase 2 (GRK2) is emerging as a physiologically relevant inhibitor of insulin signaling.ObjectivesWe tested whether lowering brain GRK2 abundance may reverse insulin‐resistance.MethodsWe lowered brain GRK2 abundance through viral‐mediated delivery of a GRK2‐specific miRNA and quantified the reversion of a developing or an established insulin‐resistant phenotype using the transgenic PLP‐SYN mouse model of MSA.ResultsViral vector delivery of a GRK2 miRNA demonstrated a neuroprotective capacity when administered (1) in utero intracerebroventricularly in developing PLP‐SYN mice and (2) intrastriatally in adult PLP‐SYN mice. Decreased striatal GRK2 levels correlated in both designs with neuroprotection of the substantia nigra dopamine neurons, reduction in high‐molecular‐weight species of α‐synuclein, and reduced insulin resistance.ConclusionsThese data support GRK2 as a potential therapeutic target in MSA. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Funder

Multiple System Atrophy Coalition

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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