Evidence map›Paper›PMID 42722646›Full record

ArticleNature communications2026

InsP3R signaling and actomyosin-dependent mitochondrial dynamics play essential roles in mitochondrial stress-induced longevity.

Gaomin Feng, Elizabeth M Ruark, Alexandra G Mulligan, Eric K F Donahue, Anthony L Hoang, Brianne Jacquet-Cribe, Li Peng, Kristopher Burkewitz

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Gaomin Feng *Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Elizabeth M Ruark *Department of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Alexandra G MulliganDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.ORCID http://orcid.org/0000-0003-0793-9865
Eric K F DonahueDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.ORCID http://orcid.org/0000-0002-7547-3959
Anthony L HoangDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Brianne Jacquet-CribeDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Li PengDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA.
Kristopher BurkewitzDepartment of Cell and Developmental Biology, Vanderbilt University, Nashville, TN, USA. kristopher.burkewitz@vanderbilt.edu.ORCID http://orcid.org/0000-0001-8531-0566

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Ben Ho Park · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI MARY Kay WASHINGTON · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI OWEN P MCGUINNESS · 2012 to 2026
$29.3M
Shop Module CoreP30EY008126 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI David J. Calkins · 1989 to 2026
$19.6M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · NIDDK · VANDERBILT UNIVERSITY · PI WASSERMAN, DAVID H · 2001 to 2015
$14.9M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
Targeting ER-mitochondrial calcium signaling to promote healthier agingR01AG073354 · NIA · VANDERBILT UNIVERSITY · PI Kristopher Burkewitz · 2022 to 2026
$1.6M
Targeting mechanisms of inter-organelle communication to promote healthy agingR00AG052666 · NIA · VANDERBILT UNIVERSITY · PI BURKEWITZ, KRISTOPHER · 2019 to 2021
$726k
NCI NIH HHS P30 CA068485NEI NIH HHS P30 EY008126NIA NIH HHS R00 AG052666NIA NIH HHS R01 AG073354NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS U24 DK059637NIH HHS P40 OD010440U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R00AG052666U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG073354
6 · The paper itself

Abstract

Certain forms of mitochondrial impairment confer longevity, while disease-associated mitochondrial dysfunction triggers pathogenesis. The adaptive pathways that distinguish benefit from pathology remain unclear. Here we reveal that longevity induced by mitochondrial Complex I/nuo-6 mutation in C. elegans is dependent on the endoplasmic reticulum (ER) Ca

Indexed as

ActomyosinCaenorhabditis elegansInositol 1,4,5-Trisphosphate ReceptorsLongevityMitochondriaMitochondrial DynamicsAnimalsCaenorhabditis elegans ProteinsCalciumCalcium ChannelsEndoplasmic ReticulumMutationSignal TransductionStress, PhysiologicalActomyosinCaenorhabditis elegans ProteinsCalciumCalcium ChannelsInositol 1,4,5-Trisphosphate Receptorsmitochondrial calcium uniporter

Identifiers

PMID42722646
PMCPMC13562621

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.