Evidence map›Paper›PMID 39980717›Full record

ArticleRegenerative therapy2025

Cell culture expansion media choice affects secretory, protective and immuno-modulatory features of adipose mesenchymal stromal cell-derived secretomes for orthopaedic applications.

Enrico Ragni, Andrea Papait, Michela Maria Taiana, Paola De Luca, Giulio Grieco, Elsa Vertua, Pietro Romele, Cecilia Colombo, Antonietta Rosa Silini, Ornella Parolini and 1 more

Abstract read
In one paragraph

Article in Regenerative therapy, 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. Review
  2. 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

11 authors.

Enrico RagniIRCCS Ospedale Galeazzi - Sant'Ambrogio, Laboratorio di Biotecnologie Applicate all'Ortopedia, Via Cristina Belgioioso 173, 20157 Milano, Italy.
Andrea PapaitDipartimento di Scienze della Vita e Sanità Pubblica, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
Michela Maria TaianaIRCCS Ospedale Galeazzi - Sant'Ambrogio, Laboratorio di Biotecnologie Applicate all'Ortopedia, Via Cristina Belgioioso 173, 20157 Milano, Italy.
Paola De LucaIRCCS Ospedale Galeazzi - Sant'Ambrogio, Laboratorio di Biotecnologie Applicate all'Ortopedia, Via Cristina Belgioioso 173, 20157 Milano, Italy.
Giulio GriecoIRCCS Ospedale Galeazzi - Sant'Ambrogio, Laboratorio di Biotecnologie Applicate all'Ortopedia, Via Cristina Belgioioso 173, 20157 Milano, Italy.
Elsa VertuaCentro di Ricerca "E. Menni", Fondazione Poliambulanza Istituto Ospedaliero, 25124 Brescia, Italy.
Pietro RomeleCentro di Ricerca "E. Menni", Fondazione Poliambulanza Istituto Ospedaliero, 25124 Brescia, Italy.
Cecilia ColomboIRCCS Ospedale Galeazzi - Sant'Ambrogio, Laboratorio di Biotecnologie Applicate all'Ortopedia, Via Cristina Belgioioso 173, 20157 Milano, Italy.
Antonietta Rosa SiliniCentro di Ricerca "E. Menni", Fondazione Poliambulanza Istituto Ospedaliero, 25124 Brescia, Italy.
Ornella ParoliniDipartimento di Scienze della Vita e Sanità Pubblica, Università Cattolica del Sacro Cuore, 00168 Roma, Italy.
Laura de GirolamoIRCCS Ospedale Galeazzi - Sant'Ambrogio, Laboratorio di Biotecnologie Applicate all'Ortopedia, Via Cristina Belgioioso 173, 20157 Milano, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Mesenchymal stromal cells (MSCs) gained attention for their anti-inflammatory and trophic properties, with musculoskeletal diseases and osteoarthritis (OA) being among the most studied conditions. Alongside cells, their released factors and extracellular vesicles (EVs), overall termed "secretome", are actively sifted being envisioned as the main therapeutic actors. In addition to standard supplementation given by foetal bovine serum (FBS) or human platelet lysate (hPL), new good manufacturing practice (GMP)-compliant serum/xeno (S/X)-free media formulations have been proposed, although their influence on MSCs phenotype and potential is scarcely described. The aim of this study is therefore to evaluate, in the OA context, the differences in secretome composition and potential after adipose-MSCs (ASCs) cultivation in both standard (FBS and hPL) and two next generation (S/X) GMP-ready supplements. Methods: Immunophenotype and secretory ability at soluble protein and EV-related levels, including embedded miRNAs, were analysed in the secretomes by means of flow cytometry, nanoparticle tracking analysis, high throughput ELISA and qRT-PCR arrays. Secretomes effect was tested in Results: Within a conserved molecular signature, a divergent fingerprint emerged for ASCs' secretomes collected after expansion in standard FBS/hPL or next-generation S/X formulations. Regarding soluble factors, a less protective feature for those in the secretome collected after ASCs were cultured in S/X media emerged. Moreover, the overall message for EV-miRNAs was characterized by a preponderance of protective signals in FBS and hPL conditions in a context of general safeguard given by ASCs released molecules. This dichotomy was reflected on secretomes' potential Conclusions: These data open the question about the implications from using new media for MSCs expansion for clinical application. Although the undeniable advantages for GMP compliant processes, this study results suggest that new media formulations would deserve a deep characterization to drive the choice of the most effective one tailored to each specific application.

Indexed as

CartilageImmune cellsMesenchymal stromal cellsOsteoarthritisRegenerative medicineSecretome

Identifiers

PMID39980717
PMCPMC11840939

What Socratic 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 Socratic graph.