Evidence map›Paper›PMID 26581954›Full record

ArticleScientific reports2015

Influence of age on rat bone-marrow mesenchymal stem cells potential.

J Fafián-Labora, P Fernández-Pernas, I Fuentes, J De Toro, N Oreiro, S Sangiao-Alvarellos, J Mateos, M C Arufe

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 73 citations in OpenAlex.

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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

8 authors at 4 institutions in 1 country.

J Fafián-LaboraGrupo de Terapia Celular y Medicina Regenerativa (TCMR-CHUAC). CIBER-BBN/ISCIII. Servicio de Reumatología. Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo Hospitalario Universitario de A Coruña (CHUAC). SERGAS. Departamento de Medicina. Facultade de Oza. Universidade de A Coruña (UDC). As Xubias, 15006. A Coruña, Spain.
P Fernández-PernasGrupo de Terapia Celular y Medicina Regenerativa (TCMR-CHUAC). CIBER-BBN/ISCIII. Servicio de Reumatología. Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo Hospitalario Universitario de A Coruña (CHUAC). SERGAS. Departamento de Medicina. Facultade de Oza. Universidade de A Coruña (UDC). As Xubias, 15006. A Coruña, Spain.
I FuentesGrupo de Terapia Celular y Medicina Regenerativa (TCMR-CHUAC). CIBER-BBN/ISCIII. Servicio de Reumatología. Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo Hospitalario Universitario de A Coruña (CHUAC). SERGAS. Departamento de Medicina. Facultade de Oza. Universidade de A Coruña (UDC). As Xubias, 15006. A Coruña, Spain.
J De ToroGrupo de Terapia Celular y Medicina Regenerativa (TCMR-CHUAC). CIBER-BBN/ISCIII. Servicio de Reumatología. Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo Hospitalario Universitario de A Coruña (CHUAC). SERGAS. Departamento de Medicina. Facultade de Oza. Universidade de A Coruña (UDC). As Xubias, 15006. A Coruña, Spain.
N OreiroGrupo de Proteómica-PBR2-ProteoRed/ISCIII-Servicio de Reumatologia. Instituto de Investigación Biomédica de A Coruña (INIBIC), Complexo Hospitalario Universitario de A Coruña (CHUAC), Sergas. Universidade da Coruña (UDC). As Xubias, 15006. A Coruña, España.
S Sangiao-AlvarellosGrupo Fisiopatología Endocrina, Nutricional y Médica (FENM-CHUAC). Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo Hospitalario Universitario de A Coruña (CHUAC). SERGAS. Departamento de Medicina. Facultade de Oza. Universidade de A Coruña (UDC). As Xubias, 15006. A Coruña, Spain.
J MateosGrupo de Terapia Celular y Medicina Regenerativa (TCMR-CHUAC). CIBER-BBN/ISCIII. Servicio de Reumatología. Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo Hospitalario Universitario de A Coruña (CHUAC). SERGAS. Departamento de Medicina. Facultade de Oza. Universidade de A Coruña (UDC). As Xubias, 15006. A Coruña, Spain.
M C ArufeGrupo de Terapia Celular y Medicina Regenerativa (TCMR-CHUAC). CIBER-BBN/ISCIII. Servicio de Reumatología. Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo Hospitalario Universitario de A Coruña (CHUAC). SERGAS. Departamento de Medicina. Facultade de Oza. Universidade de A Coruña (UDC). As Xubias, 15006. A Coruña, Spain.
Instituto de Investigación Biomédica de A Coruña · ESComplexo Hospitalario Universitario A Coruña · ESServicio Gallego de Salud · ESCentro de Investigación Biomédica en Red · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells promising role in cell-based therapies and tissue engineering appears to be limited due to a decline of their regenerative potential with increasing donor age. Six age groups from bone marrow mesenchymal stem cells of Wistar rats were studied (newborn, infant, young, pre-pubertal, pubertal and adult). Quantitative proteomic assay was performance by iTRAQ using an 8-plex iTRAQ labeling and the proteins differentially expressed were grouped in pluripotency, proliferative and metabolism processes. Proliferation makers, CD117 and Ki67 were measure by flow cytometry assay. Real time polymerase chain reaction analysis of pluripotency markers Rex1, Oct4, Sox2 and Nanog were done. Biological differentiation was realized using specific mediums for 14 days to induce osteogenesis, adipogenesis or chondrogenesis and immunostain analysis of differentiated cell resulting were done. Enzimoimmunoassay analysis of several enzymes as L-lactate dehydrogenase and glucose-6-phosphate isomerase were also done to validate iTRAQ data. Taking together these results indicate for the first time that mesenchymal stem cells have significant differences in their proliferative, pluripotency and metabolism profiles and those differences are age depending.

Indexed as

AgingAnimalsBone Marrow CellsCell ProliferationIsotope LabelingMaleMesenchymal Stem CellsPluripotent Stem CellsRats, WistarReal-Time Polymerase Chain ReactionReproducibility of ResultsSignal TransductionTOR Serine-Threonine KinasesTOR Serine-Threonine Kinases

Identifiers

PMID26581954
PMCPMC4652164
OpenAlexW2412224439

What OpenQuestion holds

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Registered trials

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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.