# Age, atherosclerosis and type 2 diabetes reduce human mesenchymal stromal cell-mediated T-cell suppression

**Authors:** Ozge Kizilay Mancini, Dominique Shum-Tim, Ursula Stochaj, José A. Correa, Inés Colmegna

PMC · DOI: 10.1186/s13287-015-0127-9 · Stem Cell Research & Therapy · 2015-08-08

## TL;DR

This study shows that aging, atherosclerosis, and type 2 diabetes reduce the ability of human mesenchymal stromal cells to suppress T-cells, which could impact cell-based therapies.

## Contribution

The study identifies age, atherosclerosis, and type 2 diabetes as factors reducing the functional potency of mesenchymal stromal cells.

## Key findings

- Advanced age reduces the T-cell suppression ability of mesenchymal stromal cells.
- Atherosclerosis and type 2 diabetes also impair the functional potency of these cells.
- Optimizing donor selection criteria could improve cell-based therapy outcomes.

## Abstract

To this end human MSCs were isolated from adipose tissue and the MSC:CD4+ T-cell suppression was assessed in a co-culture system. In summary, this study demonstrates that advanced age, atherosclerosis and type 2 diabetes mellitus reduce the functional potency of MSCs. Optimizing the criteria for the selection of MSC donors could enhance the results of cell-based therapies.

The online version of this article (doi:10.1186/s13287-015-0127-9) contains supplementary material, which is available to authorized users.

## Linked entities

- **Diseases:** atherosclerosis (MONDO:0005311), type 2 diabetes mellitus (MONDO:0005148)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, MIR335 (microRNA 335) [NCBI Gene 442904] {aka MIRN335, hsa-mir-335, miRNA335, mir-335}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}
- **Diseases:** ischemic cardiomyopathy (MESH:D009202), left ventricular dysfunction (MESH:D018487), hypoxic injury (MESH:D002534), Hypertension (MESH:D006973), death (MESH:D003643), Hypercholesterolemia (MESH:D006937), ischemic myocardium (MESH:D017682), T2DM (MESH:D003924), ATH (MESH:D050197), chronic inflammatory diseases (MESH:D002908), coronary artery disease (MESH:D003324), Chronic inflammation (MESH:D007249), ischemic (MESH:D002545), Atherosclerotic ischemic heart disease (MESH:D017202)
- **Chemicals:** CFSE (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232), MSCs — Mus musculus (Mouse), Stromal cell line (CVCL_2128)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4529693/full.md

## References

21 references — full list in the complete paper: https://tomesphere.com/paper/PMC4529693/full.md

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Source: https://tomesphere.com/paper/PMC4529693