Harlequin mice exhibit cognitive impairment, severe loss of Purkinje cells and a compromised bioenergetic status due to the absence of Apoptosis Inducing Factor.

Cerebellar ataxia Cognitive impairment Harlequin mice Mitochondria Purkinje cells

Journal

Biochimica et biophysica acta. Molecular basis of disease
ISSN: 1879-260X
Titre abrégé: Biochim Biophys Acta Mol Basis Dis
Pays: Netherlands
ID NLM: 101731730

Informations de publication

Date de publication:
17 Jun 2024
Historique:
received: 10 11 2023
revised: 15 05 2024
accepted: 27 05 2024
medline: 20 6 2024
pubmed: 20 6 2024
entrez: 19 6 2024
Statut: aheadofprint

Résumé

The functional integrity of the central nervous system relies on complex mechanisms in which the mitochondria are crucial actors because of their involvement in a multitude of bioenergetics and biosynthetic pathways. Mitochondrial diseases are among the most prevalent groups of inherited neurological disorders, affecting up to 1 in 5000 adults and despite considerable efforts around the world there is still limited curative treatments. Harlequin mice correspond to a relevant model of recessive X-linked mitochondrial disease due to a proviral insertion in the first intron of the Apoptosis-inducing factor gene, resulting in an almost complete depletion of the corresponding protein. These mice exhibit progressive degeneration of the retina, optic nerve, cerebellum, and cortical regions leading to irremediable blindness and ataxia, reminiscent of what is observed in patients suffering from mitochondrial diseases. We evaluated the progression of cerebellar degeneration in Harlequin mice, especially for Purkinje cells and its relationship with bioenergetics failure and behavioral damage. For the first time to our knowledge, we demonstrated that Harlequin mice display cognitive and emotional impairments at early stage of the disease with further deteriorations as ataxia aggravates. These functions, corresponding to higher-order cognitive processing, have been assigned to a complex network of reciprocal connections between the cerebellum and many cortical areas which could be dysfunctional in these mice. Consequently, Harlequin mice become a suitable experimental model to test innovative therapeutics, via the targeting of mitochondria which can become available to a large spectrum of neurological diseases.

Identifiants

pubmed: 38897257
pii: S0925-4439(24)00261-8
doi: 10.1016/j.bbadis.2024.167272
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

167272

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Marisol CORRAL-DEBRINSKI reports financial support was provided by French Muscular Dystrophy Association. Marisol Corral-Debrinski has patent #EP22306002.1 (Intravenous administration of neuroglobin for treating neurological disorders) pending to None. NONE If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Hélène Cwerman-Thibault (H)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France.

Vassilissa Malko-Baverel (V)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France.

Gwendoline Le Guilloux (G)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France.

Isabel Torres-Cuevas (I)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France; Department of Physiology, University of Valencia, Vicent Andrés Estellés s/n, 46100 12 Burjassot, Spain.

Edward Ratcliffe (E)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France.

Djmila Mouri (D)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France.

Virginie Mignon (V)

Université de Paris, UMR-S 1144 Inserm, 75006 Paris, France; Université Paris Cité, Platform of Cellular and Molecular Imaging, US25 Inserm, UAR3612 CNRS, 75006 Paris, France.

Bruno Saubaméa (B)

Université de Paris, UMR-S 1144 Inserm, 75006 Paris, France.

Odile Boespflug-Tanguy (O)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France; Service de Neurologie et Maladies métaboliques, CHU Paris - Hôpital Robert Debré, F-75019 Paris, France.

Pierre Gressens (P)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France.

Marisol Corral-Debrinski (M)

Université Paris Cité, NeuroDiderot, Inserm, F-75019 Paris, France. Electronic address: marisol.corral@inserm.fr.

Classifications MeSH