Evidence map›Paper›PMID 37933600›Full record

ArticleThe EMBO journal2023

Cristae formation is a mechanical buckling event controlled by the inner mitochondrial membrane lipidome.

Kailash Venkatraman, Christopher T Lee, Guadalupe C Garcia, Arijit Mahapatra, Daniel Milshteyn, Guy Perkins, Keun-Young Kim, H Amalia Pasolli, Sebastien Phan, Jennifer Lippincott-Schwartz and 3 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
8.6field-weighted citation impact, top 2% of its field
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

42 citing papers in PubMed, 56 citations in OpenAlex.

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  12. Mitochondrial mechanics nucleates axonal jamming and swelling.bioRxiv : the preprint server for biology · 2026
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  19. Homeostatic regulation of intrinsic lipid curvature in eukaryotic cells.bioRxiv : the preprint server for biology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Kailash VenkatramanDepartment of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0001-5138-7610
Christopher T Lee *Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0002-0670-2308
Guadalupe C Garcia *Computational Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, CA, USA.ORCID 0000-0002-2227-2483
Arijit Mahapatra *Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA, USA.
Daniel MilshteynDepartment of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA, USA.
Guy PerkinsNational Center for Microscopy and Imaging Research, Center for Research in Biological Systems, University of California San Diego, La Jolla, CA, USA.
Keun-Young KimNational Center for Microscopy and Imaging Research, Center for Research in Biological Systems, University of California San Diego, La Jolla, CA, USA.
H Amalia PasolliHoward Hughes Medical Institute, Ashburn, VA, USA.ORCID 0000-0003-3899-3530
Sebastien PhanNational Center for Microscopy and Imaging Research, Center for Research in Biological Systems, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0003-4261-6973
Jennifer Lippincott-SchwartzHoward Hughes Medical Institute, Ashburn, VA, USA.
Mark H EllismanNational Center for Microscopy and Imaging Research, Center for Research in Biological Systems, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0001-8893-8455
Padmini RangamaniDepartment of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0001-5953-4347
Itay BudinDepartment of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0001-9706-4294
University of California San Diego · USHoward Hughes Medical Institute · USSalk Institute for Biological Studies · US

Funding

MOLECULAR BIOPHYSICS TRAINING PROGRAMT32GM008326 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KOMIVES, ELIZABETH A. · 1989 to 2020
$7.5M
National Center for Microscopy and Imaging Research: A BRAIN Technology Integration and Dissemination ResourceU24NS120055 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2021 to 2025
$5.4M
Training in Multi-Scale Analysis of Biological Structure and FunctionT32EB009380 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrew D. McCulloch, Padmini Rangamani · 2009 to 2026
$4.8M
Lipidic drivers of organelle function and dysregulationR35GM142960 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Itay Budin · 2021 to 2026
$4.3M
3D Reconstruction and Analysis of Alzheimer's Patient Biopsy Samples to Map and Quantify Hallmarks of Pathogenesis and VulnerabilityR01AG065549 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2020 to 2024
$4.1M
The National Center for Microscopy and Imaging Research, a Community-wide Scientific ResourceR24GM137200 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ELLISMAN, MARK H · 2020 to 2022
$3.0M
Molecular Biophysics Training Grant at UC San DiegoT32GM139795 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Galia Debelouchina, ELIZABETH A. KOMIVES · 2021 to 2026
$3.0M
CRCNS: Biophysical modeling of axonal morphology and functionR01MH139350 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Padmini Rangamani · 2024 to 2026
$1.1M
JEOL JEM-1400Plus Transmission Electron MicroscopeS10OD023527 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FARQUHAR, MARILYN GIST · 2017 to 2017
$579k
NIA NIH HHS R01 AG065549NIBIB NIH HHS T32 EB009380NIGMS NIH HHS R24 GM137200NIGMS NIH HHS R35 GM142960NIGMS NIH HHS T32 GM008326NIGMS NIH HHS T32 GM139795NIH HHS S10 OD023527NIMH NIH HHS R01 MH139350NINDS NIH HHS U24 NS120055
6 · The paper itself

Abstract

Cristae are high-curvature structures in the inner mitochondrial membrane (IMM) that are crucial for ATP production. While cristae-shaping proteins have been defined, analogous lipid-based mechanisms have yet to be elucidated. Here, we combine experimental lipidome dissection with multi-scale modeling to investigate how lipid interactions dictate IMM morphology and ATP generation. When modulating phospholipid (PL) saturation in engineered yeast strains, we observed a surprisingly abrupt breakpoint in IMM topology driven by a continuous loss of ATP synthase organization at cristae ridges. We found that cardiolipin (CL) specifically buffers the inner mitochondrial membrane against curvature loss, an effect that is independent of ATP synthase dimerization. To explain this interaction, we developed a continuum model for cristae tubule formation that integrates both lipid and protein-mediated curvatures. This model highlighted a snapthrough instability, which drives IMM collapse upon small changes in membrane properties. We also showed that cardiolipin is essential in low-oxygen conditions that promote PL saturation. These results demonstrate that the mechanical function of cardiolipin is dependent on the surrounding lipid and protein components of the IMM.

Indexed as

CardiolipinsLipidomicsAdenosine TriphosphateMitochondrial MembranesPhospholipidsSaccharomyces cerevisiaeAdenosine TriphosphateCardiolipinsPhospholipidscardiolipincristaelipidsmechanicsmitochondria

Identifiers

PMID37933600
PMCPMC10711667
OpenAlexW4388456412

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.