Evidence map›Paper›PMID 32326298›Full record

ArticleCells2020

Citrate Mediates Crosstalk between Mitochondria and the Nucleus to Promote Human Mesenchymal Stem Cell In Vitro Osteogenesis.

Claudia Morganti, Massimo Bonora, Saverio Marchi, Letizia Ferroni, Chiara Gardin, Mariusz R Wieckowski, Carlotta Giorgi, Paolo Pinton, Barbara Zavan

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Bone organoids and mitochondrial reprogramming.Journal of orthopaedic translation · 2026
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  16. The critical role of cardiolipin in metazoan differentiation, development, and maturation.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
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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

9 authors at 3 institutions in 2 countries.

Claudia MorgantiDepartment of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
Massimo BonoraDepartment of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
Saverio MarchiDepartment of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
Letizia FerroniMaria Cecilia Hospital, GVM Care & Research, Via Corriera 1, Cotignola, 48033 Ravenna, Italy.
Chiara GardinMaria Cecilia Hospital, GVM Care & Research, Via Corriera 1, Cotignola, 48033 Ravenna, Italy.
Mariusz R WieckowskiLaboratory of Mitochondrial Biology and Metabolism, Nencki Institute of Experimental Biology, 02-093 Warsaw, Poland.ORCID 0000-0003-0789-4521
Carlotta GiorgiDepartment of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
Paolo PintonDepartment of Medical Sciences, University of Ferrara, 44121 Ferrara, Italy.
Barbara ZavanMaria Cecilia Hospital, GVM Care & Research, Via Corriera 1, Cotignola, 48033 Ravenna, Italy.ORCID 0000-0002-4779-4456
University of Ferrara · ITMaria Cecilia Hospital · ITInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Citrate, generated in the mitochondria, is a key metabolite that might link metabolism with signaling, chromatin structure and transcription to orchestrate mesenchymal stem cells (MSCs) fate determination. Based on a detailed morphological analysis of 3D reconstruction of mitochondria and nuclei in single cells, we identified contact sites between these organelles that drastically increase in volume and number during the early stage of mesenchymal stem cell differentiation. These contact sites create a microdomain that facilitates exchange of signals from mitochondria to the nucleus. Interestingly, we found that the citrate derived from mitochondria is necessary for osteogenic lineage determination. Indeed, inhibition of the citrate transporter system dramatically affected osteogenesis, reduced citrate levels that could be converted in α-ketoglutarate, and consequently affected epigenetic marker H3K9me3 associated with the osteogenesis differentiation process. These findings highlight that mitochondrial metabolites play key regulatory roles in the MSCs differentiation process. Further in-depth investigation is needed to provide novel therapeutic strategies in the field of regenerative medicine

Indexed as

OsteogenesisBiological TransportCell DifferentiationCell NucleusCells, CulturedCitric AcidFemaleHumansKetoglutaric AcidsMembrane Transport ProteinsMesenchymal Stem CellsMitochondriaCitric AcidKetoglutaric AcidsMembrane Transport Proteinscitratemesenchymal stem cellsmitochondrial metabolismmitochondria-nucleus communicationosteogenesisα-ketoglutarate

Identifiers

PMID32326298
PMCPMC7226543
OpenAlexW3018648762

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.