Evidence map›Paper›PMID 41865109›Full record

ArticleStem cell reviews and reports2026

Intrinsic microRNA regulatory programs define lineage-specific differentiation in human mesenchymal stem cells of different origin - dental pulp- and fat tissue-derived.

Carla Cristina G Pinheiro, Camila M Lopes-Ramos, Taro Inagaki, Paula Fontes Asprino, José Ricardo M Ferreira, Ygor Gonçalves Félix de Mattos, Helena Coutinho Geiger Campos, Jamil Award Shibli, Raphael B Parmigiani, Reza Jarrahy and 3 more

Abstract read
In one paragraph

Article in Stem cell reviews and reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

13 authors.

Carla Cristina G Pinheiro *Instituto de Ensino e Pesquisa, Hospital Sírio-Libanês, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-7613-6997
Camila M Lopes-Ramos *Instituto de Ensino e Pesquisa, Hospital Sírio-Libanês, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-0284-7371
Taro InagakiRegenerative Bioengineering and Repair Laboratory, Division of Plastic and Reconstructive Surgery, Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Paula Fontes AsprinoInstituto de Ensino e Pesquisa, Hospital Sírio-Libanês, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0002-2157-5853
José Ricardo M FerreiraRCrio Company, Campinas, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-5192-5623
Ygor Gonçalves Félix de MattosSchool of Dentistry, Faculdade Israelita de Ciências da Saúde Albert Einstein, Hospital Israelita Albert Einstein, São Paulo, 05521-200, SP, Brazil.ORCID http://orcid.org/0009-0009-1391-1421
Helena Coutinho Geiger CamposSchool of Dentistry, Faculdade Israelita de Ciências da Saúde Albert Einstein, Hospital Israelita Albert Einstein, São Paulo, 05521-200, SP, Brazil.ORCID http://orcid.org/0009-0000-7126-3084
Jamil Award ShibliDepartment of Oral Medicine, Infection and Immunity, Division of Periodontology, Harvard School of Dental Medicine, Boston, MA, USA.ORCID http://orcid.org/0000-0003-1971-0195
Raphael B ParmigianiInstituto de Ensino e Pesquisa, Hospital Sírio-Libanês, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0001-8360-3584
Reza JarrahyRegenerative Bioengineering and Repair Laboratory, Division of Plastic and Reconstructive Surgery, Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Akishige HokugoRegenerative Bioengineering and Repair Laboratory, Division of Plastic and Reconstructive Surgery, Department of Surgery, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0002-7097-3364
Alessandra V S FariaDepartamento de Biologia Celular e do Desenvolvimento, Universidade de Sao Paulo Instituto de Ciencias Biomedicas, São Paulo, SP, Brazil.ORCID http://orcid.org/0000-0003-1161-5724
Daniela Franco BuenoInstituto de Ensino e Pesquisa, Hospital Sírio-Libanês, São Paulo, SP, Brazil. daniela.bueno@einstein.br.ORCID http://orcid.org/0000-0001-5932-6134

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell fate determination and terminal differentiation are shaped by intrinsic molecular programs that coordinate lineage-specific gene expression. In mesenchymal stem cells (MSCs), variability in osteogenic efficiency among distinct tissue sources remains poorly understood and cannot be fully explained by differentiation conditions alone. Increasing evidence indicates that post-transcriptional regulatory mechanisms, particularly those mediated by microRNAs (miRNAs), are closely associated with differentiation outcomes. Here, we investigated whether intrinsic miRNA expression landscapes are associated with lineage-associated differences in late-stage mineralization, in the context of potential donor-related variability of human MSCs. Dental pulp stem cells (DPSCs) and processed lipoaspirate (PLA)-derived MSCs were cultured under identical osteogenic induction conditions and analyzed longitudinally throughout differentiation. Both cell populations fulfilled established mesenchymal phenotypic criteria and successfully initiated osteogenic commitment. However, DPSCs exhibited significantly enhanced extracellular matrix mineralization at mid-to-late stages of differentiation, suggesting divergence at later stages of extracellular matrix mineralization rather than at early lineage commitment. Temporal small RNA sequencing performed at days 0, 7, 14, and 21 revealed progressive remodeling of miRNA expression in both MSC sources. Direct comparison at the mature osteoblast stage identified a discrete set of ten miRNAs differentially expressed between DPSCs and PLA-derived cells. DPSCs displayed reduced expression of several miRNAs previously associated with inhibitory roles in osteogenic pathways. Network-based analyses indicated convergence of these miRNAs on gene programs involved in skeletal development and extracellular matrix organization. Targeted validation confirmed decreased expression of miR-10a-5p and miR-196a-5p, accompanied by increased expression of osteogenesis-associated genes, including BMP1 and MMP16, in DPSCs. Collectively, these findings show that lineage-specific miRNA expression patterns are associated with distinct osteogenic maturation trajectories in human MSCs. This work identifies an intrinsic post-transcriptional signature through which cellular origin may influence terminal differentiation outcomes and suggests that such miRNA profiles may serve as informative molecular biomarkers in the future for the selection and characterization of mesenchymal stem cells intended for human bone tissue engineering applications.

Indexed as

Adipose TissueCell DifferentiationCell LineageDental PulpMesenchymal Stem CellsMicroRNAsCells, CulturedHumansOsteogenesisMicroRNAsDental pulp stem cellMesenchymal stem cellMicroRNAOsteogenic differentiationProcessed lipoaspirate cells

Identifiers

PMID41865109
PMCPMC13099662

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.