Evidence map›Paper›PMID 41603323›Full record

ArticleAging cell2026

Disruption of ATP Synthase Spatiotemporal Organization, Ca

Silke Morris, Nico Marx, Gonzalo Barrientos, Isidora Molina-Riquelme, Frank Schmelter, Hugo E Verdejo, Stefan Peischard, Guiscard Seebohm, Verónica Eisner, Karin B Busch

Abstract read
In one paragraph

Article in Aging cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Silke MorrisInstitute of Integrative Cell Biology and Physiology, Faculty of Biology, University of Muenster, Muenster, Germany.
Nico MarxInstitute of Integrative Cell Biology and Physiology, Faculty of Biology, University of Muenster, Muenster, Germany.
Gonzalo BarrientosSchool of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile.
Isidora Molina-RiquelmeSchool of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile.
Frank SchmelterInstitute of Integrative Cell Biology and Physiology, Faculty of Biology, University of Muenster, Muenster, Germany.
Hugo E VerdejoDepartamento de Enfermedades Cardiovasculares, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile.
Stefan PeischardDepartment of Cardiovascular Medicine, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Münster, Germany.
Guiscard SeebohmDepartment of Cardiovascular Medicine, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Münster, Germany.
Verónica EisnerSchool of Biological Sciences, Pontificia Universidad Católica de Chile, Santiago de Chile, Chile.
Karin B BuschInstitute of Integrative Cell Biology and Physiology, Faculty of Biology, University of Muenster, Muenster, Germany.ORCID 0000-0003-0525-0191

Funding

Bundesministerium für Forschung, Technologie und Raumfahrt - BMFTR FKZ 01DN19046Fondo Nacional de Desarrollo Científico y Tecnológico 1191770Fondo Nacional de Desarrollo Científico y Tecnológico 1231557PCI/ANID 180060PCI/ANID 21201041
6 · The paper itself

Abstract

Heart disease is the leading cause of death in the elderly population. Age-related heart failure is frequently associated with energy deficits in cardiomyocytes. These cells rely on their abundant, cristae-rich mitochondria for ATP production. ATP synthase, localized along the cristae rims, is central to this process. It is presumed that its function is tightly bound to its spatial organization, but details remain unclear. Here, we explored the spatiotemporal organization of ATP synthase in senescent human iPSC-derived CM in conjunction with its functions. We found changes in the stoichiometry of F

Indexed as

CalciumCellular SenescenceMitochondrial Proton-Translocating ATPasesMyocardial ContractionMyocytes, CardiacAdenosine TriphosphateHumansAdenosine TriphosphateCalciumMitochondrial Proton-Translocating ATPasesATP hydrolysisATP synthase organizationcalcium dynamicscardiomyocytescontractilitycristae architecturehuman induced pluripotent stem cellsmitochondrial permeability transition pore (mPTP)senescencesingle molecule dynamics

Identifiers

PMID41603323
PMCPMC12848789

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.