Evidence map›Paper›PMID 31171801›Full record

ArticleScientific reports2019

Human osteogenic differentiation in Space: proteomic and epigenetic clues to better understand osteoporosis.

Alessandra Gambacurta, Giulia Merlini, Cristina Ruggiero, Giacomo Diedenhofen, Natalia Battista, Monica Bari, Michele Balsamo, Sara Piccirillo, Giovanni Valentini, Gabriele Mascetti and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 63 citations in OpenAlex.

  1. Epigenetics in Space: The Dynamic Cellular Response.Methods in molecular biology (Clifton, N.J.) · 2026
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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

11 authors at 5 institutions in 1 country.

Alessandra GambacurtaDepartment of Experimental Medicine, Tor Vergata University of Rome, Rome, Italy. gambacur@uniroma2.it.ORCID http://orcid.org/0000-0001-5657-1847
Giulia MerliniDepartment of Experimental Medicine, Tor Vergata University of Rome, Rome, Italy.
Cristina RuggieroDepartment of Experimental Medicine, Tor Vergata University of Rome, Rome, Italy.
Giacomo DiedenhofenDepartment of Experimental Medicine, Tor Vergata University of Rome, Rome, Italy.
Natalia BattistaFaculty of Bioscience and Technology for Food, Agriculture and Environment, University of Teramo, Teramo, Italy.
Monica BariDepartment of Experimental Medicine, Tor Vergata University of Rome, Rome, Italy.
Michele BalsamoKayser Italia S.r.l., Livorno, Italy.ORCID http://orcid.org/0000-0002-2315-4761
Sara PiccirilloItalian Space Agency, Rome, Italy.
Giovanni ValentiniItalian Space Agency, Rome, Italy.
Gabriele MascettiItalian Space Agency, Rome, Italy.
Mauro MaccarroneDepartment of Medicine, Campus Bio-Medico University of Rome, Rome, Italy. m.maccarrone@unicampus.it.ORCID http://orcid.org/0000-0002-3990-2963
University of Rome Tor Vergata · ITAgenzia Spaziale Italiana · ITKayser (Italy) · ITUniversità Campus Bio-Medico · ITUniversity of Teramo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the frame of the VITA mission of the Italian Space Agency (ASI), we addressed the problem of Space osteoporosis by using human blood-derived stem cells (BDSCs) as a suitable osteogenic differentiation model. In particular, we investigated proteomic and epigenetic changes in BDSCs during osteoblastic differentiation induced by rapamycin under microgravity conditions. A decrease in the expression of 4 embryonic markers (Sox2, Oct3/4, Nanog and E-cadherin) was found to occur to a larger extent on board the ISS than on Earth, along with an earlier activation of the differentiation process towards the osteogenic lineage. The changes in the expression of 4 transcription factors (Otx2, Snail, GATA4 and Sox17) engaged in osteogenesis supported these findings. We then ascertained whether osteogenic differentiation of BDSCs could depend on epigenetic regulation, and interrogated changes of histone H3 that is crucial in this type of gene control. Indeed, we found that H3K4me3, H3K27me2/3, H3K79me2/3 and H3K9me2/3 residues are engaged in cellular reprogramming that drives gene expression. Overall, we suggest that rapamycin induces transcriptional activation of BDSCs towards osteogenic differentiation, through increased GATA4 and Sox17 that modulate downstream transcription factors (like Runx2), critical for bone formation. Additional studies are warranted to ascertain the possible exploitation of these data to identify new biomarkers and therapeutic targets to treat osteoporosis, not only in Space but also on Earth.

Indexed as

Aerospace MedicineEpigenesis, GeneticOsteogenesisProteomeWeightlessnessBiomarkersCell DifferentiationCell LineageGATA4 Transcription FactorHistonesHumansMesenchymal Stem CellsOsteoporosisOtx Transcription FactorsProteomicsSirolimusBiomarkersGATA4 protein, humanGATA4 Transcription FactorHistonesOTX2 protein, humanOtx Transcription FactorsProteomeSirolimusSNAI1 protein, humanSnail Family Transcription FactorsSOX17 protein, humanSOXF Transcription Factors

Identifiers

PMID31171801
PMCPMC6554341
OpenAlexW2948425079

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.