Evidence map›Paper›PMID 41005297›Full record

ReviewCell chemical biology2025

Sensing within: Mitochondrial inside-out signal transduction.

Alva G Sainz, Furkan E Oflaz, Xinnan Wang

Abstract readReview
In one paragraph

Review in Cell chemical biology, 2025. 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. Mitochondrial molecular diversity in the brain.Current opinion in neurobiology · 2026
    Review
  2. The MIRO1-BAX Complex Dictates Life and Death at the Mitochondrial Gate.bioRxiv : the preprint server for biology · 2026
    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

3 authors.

Alva G SainzDepartment of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: asainz@stanford.edu.
Furkan E OflazDepartment of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305, USA.
Xinnan WangDepartment of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address: xinnanw@stanford.edu.

Funding

Molecular Regulations of Mitochondrial Structure in Neuronal Homeostasis and SurvivalR01NS128040 · NINDS · STANFORD UNIVERSITY · PI XINNAN WANG · 2022 to 2026
$2.2M
Regulation of mitochondrial motility and mitophagy by LRRK2.R01NS089583 · NINDS · STANFORD UNIVERSITY · PI WANG, XINNAN · 2014 to 2018
$2.0M
A control center for mitochondrial navigation in neuronsR01GM143258 · NIGMS · STANFORD UNIVERSITY · PI WANG, XINNAN · 2021 to 2024
$1.5M
NIGMS NIH HHS R01 GM143258NINDS NIH HHS R01 NS089583NINDS NIH HHS R01 NS128040
6 · The paper itself

Abstract

The prevailing theory on the origins of mitochondria proposes that they were once independent organisms. Though symbiotically integrated into eukaryotic cells, they have retained a striking degree of autonomy. This self-governance manifests as the capacity to sense internal metabolic, ionic, and redox states and transduce these into signals that modulate cellular function-a process we refer to as mitochondrial inside-out signaling. These mitochondria-initiated signaling mechanisms are crucial for bioenergetic homeostasis of all cells, including neurons. Unlike conventional outside-in signaling, these mitochondria-initiated signals stem from within the organelle and propagate outward, tuning cytosolic signaling pathways, nuclear transcriptional programs, and neuronal behavior. In this review, we provide mechanistic insights into this distinct and underappreciated signaling modality, discussing how internal mitochondrial conditions are sensed and transmitted to the cytosol and how these signaling events influence mitochondrial and cellular health with a focus on their implications for neuronal physiology and disease vulnerability.

Indexed as

MitochondriaSignal TransductionAnimalsCytosolHumansNeuronsmitochondrial inside-out signalingmitochondrial retrograde signalingneurodegenerationneurosciencesignal transduction

Identifiers

PMID41005297
PMCPMC12479096

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.