Defective dimerization of FoF1‐ATP synthase secondary to glycation favors mitochondrial energy deficiency in cardiomyocytes during aging-Reference-Cited by-同舟云学术

Defective dimerization of FoF1‐ATP synthase secondary to glycation favors mitochondrial energy deficiency in cardiomyocytes during aging

Published:2022-03 Issue:3 Volume:21 Page:
ISSN:1474-9718
Container-title:Aging Cell
language:en
Short-container-title:Aging Cell

Author:

Bou‐Teen Diana¹²,Fernandez‐Sanz Celia³,Miro‐Casas Elisabet¹²,Nichtova Zuzana⁴,Bonzon‐Kulichenko Elena²⁵,Casós Kelly¹²,Inserte Javier¹²,Rodriguez‐Sinovas Antonio¹²,Benito Begoña¹²,Sheu Shey‐Shing³,Vázquez Jesús²⁵,Ferreira‐González Ignacio¹,Ruiz‐Meana Marisol¹²^ORCID

Affiliation:

1. Cardiovascular Diseases Research Group Vall d’Hebron Institut de Recerca (VHIR) Vall d’Hebron Hospital Universitari Barcelona Spain

2. Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBER‐CV) Madrid Spain

3. Center for Translational Medicine Department of Medicine Thomas Jefferson University Philadelphia Pennsylvania USA

4. Cardiovascular Proteomics Laboratory Centro Nacional de Investigaciones Cardiovasculares Carlos III Madrid Spain

5. MitoCare Center for Mitochondrial Imaging Research and Diagnostics Department of Pathology Anatomy & Cell Biol. Thomas Jefferson University Philadelphia Pennsylvania USA

Funder

Instituto de Salud Carlos III

Publisher

Wiley

Subject

Cell Biology,Aging

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/acel.13564

Reference47 articles.

1. An uncoupling channel within the c-subunit ring of the F1FO ATP synthase is the mitochondrial permeability transition pore

2. Aging shifts mitochondrial dynamics toward fission to promote germline stem cell loss

3. Mitochondrial ATP synthase dimers spontaneously associate due to a long-range membrane-induced force