Dose-Dependent Immunomodulatory Effect of Human Stem Cells from Amniotic Membrane: A Comparison with Human Mesenchymal Stem Cells from Adipose Tissue

间充质干细胞 脂肪组织 外周血单个核细胞 干细胞 羊膜干细胞 羊膜上皮细胞 免疫学 免疫系统 造血 骨髓 细胞生物学 干细胞移植修复关节软骨 组织工程 化学 癌症研究 成体干细胞 生物 医学 内皮干细胞 体外 生物医学工程 生物化学
作者
Susanne Wolbank,Anja Peterbauer,Marc Fahrner,Simone Hennerbichler,Martijn van Griensven,Guido Stadler,Heinz Redl,Christian Gabriel
出处
期刊:Tissue Engineering [Mary Ann Liebert, Inc.]
卷期号:13 (6): 1173-1183 被引量:363
标识
DOI:10.1089/ten.2006.0313
摘要

Bone marrow-derived mesenchymal stem cells (BMSCs) have been used for allogeneic application in tissue engineering but have certain drawbacks. Therefore, stem cells (SC)s derived from other adult tissue sources have been considered as an alternative. However, there is only limited knowledge on their immunomodulatory properties. The aim of our study was to compare the immunomodulatory potential of human amniotic mesenchymal and human amniotic epithelial cells with that of human adipose-derived SCs under identical experimental conditions. We have demonstrated a dose-dependent inhibition of peripheral blood mononuclear cell (PBMC) immune responses in mixed lymphocyte reactions (up to 66-93% inhibition) and phytohemagglutinin activation assays (up to 67-96% inhibition). The lowest SC-to-PBMC ratio able to inhibit PBMC proliferation significantly was 1:8. Subcultivation (passage 2-6) did not alter immunoinhibitory properties, whereas cryopreservation significantly reduced the immunomodulatory potential. Using transwell systems, we have demonstrated an inhibition mechanism that is dependent on cell contact. Additionally, in coculture with allogeneic PBMCs, SCs were well tolerated and at most provoked mild alloreactions in singular cases. This study demonstrates, for the first time, contact- and dose-dependent immunosuppression of mesenchymal and epithelial amniotic SC populations, as well as of adipose tissue-derived SCs. All three cell types may be considered as possible alternatives to BMSCs for allogeneic application in tissue engineering.
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