The Q-junction and the inflammatory response are critical pathological and therapeutic factors in CoQ deficiency

Pilar González-García, María Elena Díaz-Casado, Agustín Hidalgo-Gutiérrez, Laura Jiménez-Sánchez, Mohammed Bakkali, Eliana Barriocanal-Casado, Germaine Escames, Riccardo Zenezini Chiozzi, Franziska Völlmy, Esther A. Zaal, Celia R. Berkers, Albert J.R. Heck, Luis C. López*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Defects in Coenzyme Q (CoQ) metabolism have been associated with primary mitochondrial disorders, neurodegenerative diseases and metabolic conditions. The consequences of CoQ deficiency have not been fully addressed, and effective treatment remains challenging. Here, we use mice with primary CoQ deficiency (Coq9R239X), and we demonstrate that CoQ deficiency profoundly alters the Q-junction, leading to extensive changes in the mitochondrial proteome and metabolism in the kidneys and, to a lesser extent, in the brain. CoQ deficiency also induces reactive gliosis, which mediates a neuroinflammatory response, both of which lead to an encephalopathic phenotype. Importantly, treatment with either vanillic acid (VA) or β-resorcylic acid (β-RA), two analogs of the natural precursor for CoQ biosynthesis, partially restores CoQ metabolism, particularly in the kidneys, and induces profound normalization of the mitochondrial proteome and metabolism, ultimately leading to reductions in gliosis, neuroinflammation and spongiosis and, consequently, reversing the phenotype. Together, these results provide key mechanistic insights into defects in CoQ metabolism and identify potential disease biomarkers. Furthermore, our findings clearly indicate that the use of analogs of the CoQ biosynthetic precursor is a promising alternative therapy for primary CoQ deficiency and has potential for use in the treatment of more common neurodegenerative and metabolic diseases that are associated with secondary CoQ deficiency.

Original languageEnglish
Article number102403
JournalRedox Biology
Volume55
DOIs
Publication statusPublished - Sept 2022

Bibliographical note

Funding Information:
English edition has been provided by Springer Nature Author Services. We thank members of the Heck Lab for their support in analyzing the proteomics samples. This work was supported by grants from the MCIN/AEI/10.13039/501100011033, Spain, and the ERDF (RTI2018-093503-B-100); the Muscular Dystrophy Association (MDA-602322); the Junta de Andalucía (grant numbers P20_00134 and PEER-0083-2020); and by EPIC-XS, project number 823839, funded by the Horizon 2020 programme of the European Union. P. P.G.-G. is ‘FPU fellow’ from the Ministerio de Universidades, Spain. A.H.-G. is supported by the “Plan Propio de Investigación” from the University of Granada. L.J. and E.B.-C. are supported by the Consejería de Salud, Junta de Andalucía, Spain.

Funding Information:
English edition has been provided by Springer Nature Author Services. We thank members of the Heck Lab for their support in analyzing the proteomics samples. This work was supported by grants from the MCIN/ AEI /10.13039/501100011033, Spain, and the ERDF ( RTI2018-093503-B-100 ); the Muscular Dystrophy Association ( MDA-602322 ); the Junta de Andalucía (grant numbers P20_00134 and PEER-0083-2020 ); and by EPIC-XS, project number 823839, funded by the Horizon 2020 programme of the European Union . P. P.G.-G. is ‘FPU fellow’ from the Ministerio de Universidades, Spain. A.H.-G. is supported by the “Plan Propio de Investigación” from the University of Granada . L.J. and E.B.-C. are supported by the Consejería de Salud, Junta de Andalucía, Spain.

Publisher Copyright:
© 2022 The Authors

Funding

English edition has been provided by Springer Nature Author Services. We thank members of the Heck Lab for their support in analyzing the proteomics samples. This work was supported by grants from the MCIN/AEI/10.13039/501100011033, Spain, and the ERDF (RTI2018-093503-B-100); the Muscular Dystrophy Association (MDA-602322); the Junta de Andalucía (grant numbers P20_00134 and PEER-0083-2020); and by EPIC-XS, project number 823839, funded by the Horizon 2020 programme of the European Union. P. P.G.-G. is ‘FPU fellow’ from the Ministerio de Universidades, Spain. A.H.-G. is supported by the “Plan Propio de Investigación” from the University of Granada. L.J. and E.B.-C. are supported by the Consejería de Salud, Junta de Andalucía, Spain. English edition has been provided by Springer Nature Author Services. We thank members of the Heck Lab for their support in analyzing the proteomics samples. This work was supported by grants from the MCIN/ AEI /10.13039/501100011033, Spain, and the ERDF ( RTI2018-093503-B-100 ); the Muscular Dystrophy Association ( MDA-602322 ); the Junta de Andalucía (grant numbers P20_00134 and PEER-0083-2020 ); and by EPIC-XS, project number 823839, funded by the Horizon 2020 programme of the European Union . P. P.G.-G. is ‘FPU fellow’ from the Ministerio de Universidades, Spain. A.H.-G. is supported by the “Plan Propio de Investigación” from the University of Granada . L.J. and E.B.-C. are supported by the Consejería de Salud, Junta de Andalucía, Spain.

Keywords

  • Coenzyme Q
  • Mitochondrial disease
  • Omics
  • Phenolic compound
  • Therapy

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