Human embryonic stem cell derived-mesenchymal stem cells: an alternative mesenchymal stem cell source for regenerative medicine therapy

被引:1
|
作者
Gadkari, Rishali [1 ]
Zhao, Longmei [2 ]
Teklemariam, Takele [2 ]
Hantash, Basil M. [2 ,3 ]
机构
[1] San Jose State Univ, San Jose, CA 95192 USA
[2] Escape Therapeut Inc, San Jose, CA 95138 USA
[3] Elixir Inst Regenerat Med, San Jose, CA 95138 USA
关键词
AMSC; BMSC; differentiation; growth kinetics; hESC-MSC; immunosuppression; UMBILICAL-CORD BLOOD; HUMAN BONE-MARROW; ADIPOSE-TISSUE; STROMAL CELLS; OSTEOGENIC DIFFERENTIATION; GENE-EXPRESSION; TRANSPLANTATION; DERIVATION; CULTURE; VIVO;
D O I
10.2217/RME.14.13
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Aim: To enumerate and characterize mesenchymal stem cells (MSC) derived from human embryonic stem cells (hESC) for clinical application. Materials & methods: hESC were differentiated into hESC-MSC and characterized by the expression of surface markers using flow cytometry. hESC-MSC were evaluated with respect to growth kinetics, colony-forming potential, as well as osteogenic and adipogenic differentiation capacity. Immunosuppressive effects were assessed using peripheral blood mononuclear cell (PBMC) proliferation and cytotoxicity assays. Results: hESC-MSC showed similar morphology, and cell surface markers as adipose (AMSC) and bone marrow-derived MSC (BMSC). hESC-MSC exhibited a higher growth rate during early in vitro expansion and equivalent adipogenic and osteogenic differentiation and colony-forming potential as AMSC and BMSC. hESC-MSC demonstrated similar immunosuppressive effects as AMSC and BMSC. Conclusion: hESC-MSC were comparable to BMSC and AMSC and hence can be used as an alternative source of MSC for clinical applications.
引用
收藏
页码:453 / 465
页数:13
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