Evidence map›Paper›PMID 41654866›Full record

ReviewJournal of translational medicine2026

The importance of mitochondria and mitochondrial calcium signaling in health and disease: an updated outlook on inflammation.

Giampaolo Morciano, Giulia Pellielo, Esther Densu Agyapong, Cristina Pellegrino, Simone Patergnani, Davide Franceschini, Konstantinos Koutsikos, Leonardo Rigon, Paolo Pinton, Alessandro Rimessi

Abstract readReview
In one paragraph

Review in Journal of translational medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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.

Giampaolo MorcianoDepartment of Biosciences, Biotechnology and Environment, University of Bari "Aldo Moro", Bari, Italy. giampaolo.morciano@uniba.it.
Giulia PellieloSection of Experimental Medicine and Laboratory for Technologies of Advanced Therapies (LTTA), Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Esther Densu AgyapongSection of Experimental Medicine and Laboratory for Technologies of Advanced Therapies (LTTA), Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Cristina PellegrinoSection of Experimental Medicine and Laboratory for Technologies of Advanced Therapies (LTTA), Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Simone PatergnaniSection of Experimental Medicine and Laboratory for Technologies of Advanced Therapies (LTTA), Department of Medical Sciences, University of Ferrara, Ferrara, Italy.
Davide FranceschiniIRCCS San Camillo Hospital, Venice, Italy.
Konstantinos KoutsikosIRCCS San Camillo Hospital, Venice, Italy.
Leonardo RigonIRCCS San Camillo Hospital, Venice, Italy.
Paolo PintonMaria Cecilia Hospital, GVM Care & Research, Cotignola, Italy. paolo.pinton@unife.it.
Alessandro RimessiSection of Experimental Medicine and Laboratory for Technologies of Advanced Therapies (LTTA), Department of Medical Sciences, University of Ferrara, Ferrara, Italy. alessandro.rimessi@unife.it.ORCID 0000-0001-7091-5765

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMitochondria are central regulators of cellular bioenergetics, calcium homeostasis and apoptosis. Beyond these classical roles, emerging evidence highlights their pivotal involvement in inflammation and related disease progression. Under physiological conditions, mitochondria sustain metabolism and signaling; however, when dysfunctional, they can release mitochondrial damage-associated molecular patterns, such as mitochondrial DNA, reactive oxygen species, cardiolipin and ATP, into the intra- or extracellular environment. MAIN BODY: The release of these mitochondrial components activates innate immune receptors and inflammasomes, thereby initiating or sustaining inflammatory cascades implicated in aging and a broad range of diseases, including cancer and neurodegenerative, cardiovascular, gastrointestinal and respiratory disorders. Mitochondrial calcium signaling plays a crucial role in energy production and metabolic adaptation; yet when dysregulated, it promotes ROS generation, membrane permeabilization and cell death, all of which further amplify inflammation. Structural and functional mitochondrial messengers, including mtDNA fragments and mitochondria-derived vesicles, also contribute to intercellular communication, enhancing immune activation or driving chronic inflammation depending on their context. Therapeutically, mitochondria are emerging as promising targets to counteract inflammation. Investigational strategies include mitochondrial transplantation, engineered mitovesicles, pharmacological modulators of Ca2 + flux, antioxidants, and agents that restore mitochondrial biogenesis and metabolism. By reestablishing mitochondrial integrity, these interventions aim to reduce inflammatory signaling, restore cellular homeostasis, and slow disease progression.

conclusionsThis review underscores mitochondria as both initiators and regulators of inflammatory processes across multiple diseases, highlighting their dual role as drivers of pathology and as promising therapeutic targets. A deeper understanding of mitochondrial signaling, mitochondrial messengers, and inter-organelle communication will be essential for developing effective mitochondria-based therapies to mitigate inflammation and improve patient outcomes.

Indexed as

Calcium SignalingDiseaseHealthInflammationMitochondriaAnimalsHumansAgingCancerCardiovascular diseasesIBDInflammationMitochondriaMitochondria targeted-therapymtDNANeurodegenerative diseasesRespiratory diseasesROS

Identifiers

PMID41654866
PMCPMC12977683

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.