Evidence map›Paper›PMID 26815002›Full record

ArticleCytotechnology2016

Human adipose derived mesenchymal stromal cells transduced with GFP lentiviral vectors: assessment of immunophenotype and differentiation capacity in vitro.

Fiona A van Vollenstee, Carlo Jackson, Danie Hoffmann, Marnie Potgieter, Chrisna Durandt, Michael S Pepper

Open access · hybridAbstract read
In one paragraph

Article in Cytotechnology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Isolation and Characterization of Equine Mesenchymal Stromal/Stem Cells.Methods in molecular biology (Clifton, N.J.) · 2025
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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

6 authors at 1 institution in 1 country.

Fiona A van VollensteeDepartment of Immunology, Faculty of Health Sciences, Institute for Cellular and Molecular Medicine and MRC Extramural Unit for Stem Cell Research and Therapy, University of Pretoria, P.O. Box 2034, Pretoria, 0001, South Africa.
Carlo JacksonDepartment of Immunology, Faculty of Health Sciences, Institute for Cellular and Molecular Medicine and MRC Extramural Unit for Stem Cell Research and Therapy, University of Pretoria, P.O. Box 2034, Pretoria, 0001, South Africa.
Danie HoffmannPlastic and Reconstructive Surgeon, Private Practice, Pretoria, South Africa.
Marnie PotgieterDepartment of Immunology, Faculty of Health Sciences, Institute for Cellular and Molecular Medicine and MRC Extramural Unit for Stem Cell Research and Therapy, University of Pretoria, P.O. Box 2034, Pretoria, 0001, South Africa.
Chrisna DurandtDepartment of Immunology, Faculty of Health Sciences, Institute for Cellular and Molecular Medicine and MRC Extramural Unit for Stem Cell Research and Therapy, University of Pretoria, P.O. Box 2034, Pretoria, 0001, South Africa.
Michael S PepperDepartment of Immunology, Faculty of Health Sciences, Institute for Cellular and Molecular Medicine and MRC Extramural Unit for Stem Cell Research and Therapy, University of Pretoria, P.O. Box 2034, Pretoria, 0001, South Africa. michael.pepper@up.ac.za.
University of Pretoria · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adipose derived mesenchymal stromal/stem cells (ASCs) are a heterogeneous population characterized by (a) their ability to adhere to plastic; (b) immunophenotypic expression of certain cell surface markers, while lacking others; and (c) the capacity to differentiate into lineages of mesodermal origin including osteocytes, chondrocytes and adipocytes. The long-term goal is to utilize these cells for clinical translation into cell-based therapies. However, preclinical safety and efficacy need to be demonstrated in animal models. ASCs can also be utilized as biological vehicles for vector-based gene delivery systems, since they are believed to home to sites of inflammation and infection in vivo. These factors motivated the development of a labelling system for ASCs using lentiviral vector-based green fluorescent protein (GFP) transduction. Human ASCs were transduced with GFP-expressing lentiviral vectors. A titration study determined the viral titer required to transduce the maximum number of ASCs. The effect of the transduced GFP lentiviral vector on ASC immunophenotypic expression of surface markers as well as their ability to differentiate into osteocytes and adipocytes were assessed in vitro. A transduction efficiency in ASC cultures of approximately 80 % was observed with an MOI of ~118. No significant immunophenotypic differences were observed between transduced and non-transduced cells and both cell types successfully differentiated into adipocytes and osteocytes in vitro. We obtained >80 % transduction of ASCs using GFP lentiviral vectors. Transduced ASCs maintained plastic adherence, demonstrated ASC immunophenotype and the ability to differentiate into cells of the mesodermal lineage. This GFP-ASC transduction technique offers a potential tracking system for future pre-clinical studies.

Indexed as

Adipose derived stromal/stem cells (ASCs)ASC labelingGreen fluorescent protein (GFP)Lentiviral vectorViral transduction

Identifiers

PMID26815002
PMCPMC5023578
OpenAlexW2298101332

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.