Multicentric Standardization of Protocols for the Diagnosis of Human Mitochondrial Respiratory Chain Defects.

diagnosis enzyme activity mitochondrial disease mitochondrial respiratory chain standardization

Journal

Antioxidants (Basel, Switzerland)
ISSN: 2076-3921
Titre abrégé: Antioxidants (Basel)
Pays: Switzerland
ID NLM: 101668981

Informations de publication

Date de publication:
08 Apr 2022
Historique:
received: 02 02 2022
revised: 30 03 2022
accepted: 01 04 2022
entrez: 23 4 2022
pubmed: 24 4 2022
medline: 24 4 2022
Statut: epublish

Résumé

The quantification of mitochondrial respiratory chain (MRC) enzymatic activities is essential for diagnosis of a wide range of mitochondrial diseases, ranging from inherited defects to secondary dysfunctions. MRC lesion is frequently linked to extended cell damage through the generation of proton leak or oxidative stress, threatening organ viability and patient health. However, the intrinsic challenge of a methodological setup and the high variability in measuring MRC enzymatic activities represents a major obstacle for comparative analysis amongst institutions. To improve experimental and statistical robustness, seven Spanish centers with extensive experience in mitochondrial research and diagnosis joined to standardize common protocols for spectrophotometric MRC enzymatic measurements using minimum amounts of sample. Herein, we present the detailed protocols, reference ranges, tips and troubleshooting methods for experimental and analytical setups in different sample preparations and tissues that will allow an international standardization of common protocols for the diagnosis of MRC defects. Methodological standardization is a crucial step to obtain comparable reference ranges and international standards for laboratory assays to set the path for further diagnosis and research in the field of mitochondrial diseases.

Identifiants

pubmed: 35453428
pii: antiox11040741
doi: 10.3390/antiox11040741
pmc: PMC9027926
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Instituto de Salud Carlos III
ID : PI17/00359
Organisme : Instituto de Salud Carlos III
ID : PI18/00498
Organisme : Instituto de Salud Carlos III
ID : PI18/00451
Organisme : Instituto de Salud Carlos III
ID : PI19/01772
Organisme : Instituto de Salud Carlos III
ID : PI21/00935
Organisme : Centre for Biomedical Network Research on Rare Diseases
ID : ISCIII-FEDER

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Auteurs

Nuria Bujan (N)

Inborn Errors of Metabolism Section (IBC U737), Molecular Genetics and Biochemistry Service, Hospital Clínic of Barcelona, IDIBAPS, 08036 Barcelona, Spain.

Constanza Morén (C)

Muscle Research and Mitochondrial Function Laboratory (U722), Cellex-IDIBAPS, Faculty of Medicine and Health Sciences-University of Barcelona, Internal Medicine Department-Hospital Clínic of Barcelona, 08036 Barcelona, Spain.

Francesc J García-García (FJ)

Muscle Research and Mitochondrial Function Laboratory (U722), Cellex-IDIBAPS, Faculty of Medicine and Health Sciences-University of Barcelona, Internal Medicine Department-Hospital Clínic of Barcelona, 08036 Barcelona, Spain.

Alberto Blázquez (A)

Mitochondrial Diseases Laboratory (U723), Research Institute, Universitary Hospital 12 de Octubre (Imas12), 28041 Madrid, Spain.

Clara Carnicer (C)

Laboratory of Inborn Errors of Metabolism, Biochemistry Service (U701), Laboratoris Clínics, Universitary Hospital Vall d'Hebron, 08035 Barcelona, Spain.

Ana Belén Cortés (AB)

Bioenergetics and Cell Physiology Service (U729), Central Services of Research, University Pablo de Olavide, 41013 Sevilla, Spain.

Cristina González (C)

Biochemistry Department (U717), Biomedical Research Institute 'Alberto Sols', CSIC, Faculty of Medicine, Autonomous University of Madrid, and Instituto de Investigación Sanitaria Hospital 12 de Octubre (Imas12), 28041 Madrid, Spain.

Ester López-Gallardo (E)

Cell and Molecular Biology Department (U727), Veterinary Faculty, University of Zaragoza, 50009 Zaragoza, Spain.

Ester Lozano (E)

Department of Cell Biology, Physiology and Immunology, Faculty of Biology, Universitat de Barcelona (UB), and Institute of Biomedicine of the University of Barcelona (IBUB), 08007 Barcelona, Spain.

Sonia Moliner (S)

Inborn Errors of Metabolism Section (IBC U737), Molecular Genetics and Biochemistry Service, Hospital Clínic of Barcelona, IDIBAPS, 08036 Barcelona, Spain.

Laura Gort (L)

Inborn Errors of Metabolism Section (IBC U737), Molecular Genetics and Biochemistry Service, Hospital Clínic of Barcelona, IDIBAPS, 08036 Barcelona, Spain.

Ester Tobías (E)

Muscle Research and Mitochondrial Function Laboratory (U722), Cellex-IDIBAPS, Faculty of Medicine and Health Sciences-University of Barcelona, Internal Medicine Department-Hospital Clínic of Barcelona, 08036 Barcelona, Spain.

Aitor Delmiro (A)

Mitochondrial Diseases Laboratory (U723), Research Institute, Universitary Hospital 12 de Octubre (Imas12), 28041 Madrid, Spain.

Miguel Ángel Martin (MÁ)

Mitochondrial Diseases Laboratory (U723), Research Institute, Universitary Hospital 12 de Octubre (Imas12), 28041 Madrid, Spain.

Miguel Ángel Fernández-Moreno (MÁ)

Biochemistry Department (U717), Biomedical Research Institute 'Alberto Sols', CSIC, Faculty of Medicine, Autonomous University of Madrid, and Instituto de Investigación Sanitaria Hospital 12 de Octubre (Imas12), 28041 Madrid, Spain.

Eduardo Ruiz-Pesini (E)

Cell and Molecular Biology Department (U727), Veterinary Faculty, University of Zaragoza, 50009 Zaragoza, Spain.

Elena Garcia-Arumí (E)

Mitochondrial Pathology Laboratory, Research Institute, Universitary Hospital Vall d'Hebron, 08035 Barcelona, Spain.

Juan Carlos Rodríguez-Aguilera (JC)

Bioenergetics and Cell Physiology Service (U729), Central Services of Research, University Pablo de Olavide, 41013 Sevilla, Spain.

Glòria Garrabou (G)

Muscle Research and Mitochondrial Function Laboratory (U722), Cellex-IDIBAPS, Faculty of Medicine and Health Sciences-University of Barcelona, Internal Medicine Department-Hospital Clínic of Barcelona, 08036 Barcelona, Spain.

Classifications MeSH