Evidence map›Paper›PMID 28866844›Full record

ArticleCytotechnology2018

Generation and characterization of transgenic mouse mesenchymal stem cell lines expressing hIGF-1 or hG-CSF.

Gabrielle V M Gonçalves, Daniela N Silva, Rejane H Carvalho, Bruno S F Souza, Kátia Nunes da Silva, Juliana F Vasconcelos, Bruno D Paredes, Carolina K V Nonaka, Ricardo Ribeiro-Dos-Santos, Milena B P Soares

Open access · greenAbstract read
In one paragraph

Article in Cytotechnology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 12 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

10 authors at 1 institution in 1 country.

Gabrielle V M GonçalvesCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Daniela N SilvaCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Rejane H CarvalhoCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Bruno S F SouzaCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Kátia Nunes da SilvaCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Juliana F VasconcelosCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Bruno D ParedesCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Carolina K V NonakaCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Ricardo Ribeiro-Dos-SantosCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil.
Milena B P SoaresCenter for Biotechnology and Cell Therapy, Hospital São Rafael, Salvador, BA, 41253-190, Brazil. milena@bahia.fiocruz.br.ORCID http://orcid.org/0000-0001-7549-2992
Hospital São Rafael · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSC) are promising tools in the fields of cell therapy and regenerative medicine. In addition to their differentiation potential, MSC have the ability to secrete bioactive molecules that stimulate tissue regeneration. Thus, the overexpression of cytokines and growth factors may enhance the therapeutic effects of MSC. Here we generated and characterized mouse bone marrow MSC lines overexpressing hG-CSF or hIGF-1. MSC lines overexpressing hG-CSF or hIGF-1 were generated through lentiviral vector mediated gene transfer. The expression of hG-CSF or hIGF-1 genes in the clones produced was quantified by qRT-PCR, and the proteins were detected in the cell supernatants by ELISA. The cell lines displayed cell surface markers and differentiation potential into adipocytes, osteocytes and chondrocytes similar to the control MSC cell lines, indicating the conservation of their phenotype even after genetic modification. IGF-1 and G-CSF transgenic cells maintained immunosuppressive activity. Finally, we performed a comparative gene expression analysis by qRT-PCR array in the cell lines expressing hIGF-1 and hG-CSF when compared to the control cells. Our results demonstrate that the cell lines generated may be useful tools for cell therapy and are suitable for testing in disease models.

Indexed as

G-CSFGrowth factorsIGF-1Mesenchymal stem cells

Identifiers

PMID28866844
PMCPMC5851953
OpenAlexW2751555721

What OpenQuestion 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 OpenQuestion graph.