Evidence map›Paper›PMID 40501800›Full record

ArticlebioRxiv : the preprint server for biology2025

Mitochondrial fusion controls the development of specialized mitochondrial structure and metabolism in rod photoreceptor cells.

Michael Landowski, Ryo Hagimori, Purnima Gogoi, Vijesh J Bhute, Sakae Ikeda, Tetsuya Takimoto, Akihiro Ikeda

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

7 authors.

Michael LandowskiDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Ryo HagimoriDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Purnima GogoiDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Vijesh J BhuteDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Sakae IkedaDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.
Tetsuya TakimotoOncology Innovation Center, Fujita Health University, Toyoake, Aichi, Japan.
Akihiro IkedaDepartment of Medical Genetics, University of Wisconsin-Madison, Madison, Wisconsin, United States of America.

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI Justine Yang Bruce · 1985 to 2026
$142.6M
UW Vision Research Core - Administrative CoreP30EY016665 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI AKIHIRO IKEDA · 2005 to 2026
$12.6M
Molecular Genetics of Age-Dependent Retinal DegenerationR01EY022086 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI AKIHIRO IKEDA · 2012 to 2026
$6.1M
Vision Research Training ProgramT32EY027721 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI ROBERT W NICKELLS · 2018 to 2026
$1.5M
Role of mitochondrial dynamics in rod photoreceptor cellsR01EY036383 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI AKIHIRO IKEDA · 2024 to 2026
$1.2M
Automated Tissue MicroarrayerS10OD023526 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI MATKOWSKYJ, KRISTINA A. · 2018 to 2018
$184k
The Function of Transmembrane Protein 135 in Retinal Pigmented EpitheliumF32EY032766 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI LANDOWSKI, MICHAEL · 2021 to 2022
$117k
NCI NIH HHS P30 CA014520NEI NIH HHS F32 EY032766NEI NIH HHS P30 EY016665NEI NIH HHS R01 EY022086NEI NIH HHS R01 EY036383NEI NIH HHS T32 EY027721NIH HHS S10 OD023526
6 · The paper itself

Abstract

Mitochondria are dynamic organelles that undergo continuous morphological changes, yet exhibit unique, cell-type-specific structures. In rod photoreceptor cells of the retina, these structures include elongated mitochondria in the inner segments and a distinct, large, circular mitochondrion in each presynaptic terminal. The mechanisms underlying the establishment and maintenance of these specialized mitochondrial morphologies, along with their functional significance, are not well understood. Here, we investigate the roles of mitochondrial fusion proteins mitofusin 1 (MFN1) and mitofusin 2 (MFN2) in shaping these structures and maintaining photoreceptor cell health. Rod photoreceptor cell-specific ablation of MFN1 and MFN2 resulted in mitochondrial fragmentation by one month of age, suggesting that mitochondrial fusion is essential for the development of photoreceptor cell-specific mitochondrial structures. Notably, the layer structures of the retina examined by light microscopy appeared unaffected at this age. Following this time period, significant photoreceptor cell degeneration occurred by three months of age. Furthermore, we showed that impaired mitochondrial fusion perturbed the balance of proteins involved in glycolysis, oxidative phosphorylation (OXPHOS), and β-oxidation, highlighting the critical role of mitochondrial fusion in ensuring the proper levels of proteins necessary for optimal energy metabolism. Additionally, we identified upregulation of cellular stress pathways such as endoplasmic reticulum (ER) stress and unfolded protein response (UPR), which arise in response to energy deprivation, and cytoprotective biosynthetic pathways mediated by CCAAT/enhancer-binding protein gamma (C/EBPγ) and mammalian target of rapamycin complex 1 (mTORC1) signaling. In summary, our findings indicate that mitochondrial fusion through MFN1 and MFN2 is vital for the development of unique mitochondrial structures and proper energy production, underscoring the fundamental importance of mitochondrial dynamics in photoreceptor cell function and survival.

Indexed as

Metabolic alterationMitochondriaMorphologyRetinaRod photoreceptor cells

Identifiers

PMID40501800
PMCPMC12154637

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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.