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Updated: Oct 14, 2025

Assessment of the Immunomodulatory Properties of Human Mesenchymal Stem Cells MSCs
Published on: December 24, 2015
Functional characterization of the immunomodulatory properties of human urine-derived stem cells
Rongpei Wu1,2, Melisa Soland1, Guihua Liu1,3
1Wake Forest Institute for Regenerative Medicine, Wake Forest University, Winston Salem, NC, USA.
Insights
Human urine-derived stem cells (USCs) show significant immunomodulatory properties, secreting cytokines that suppress immune cell proliferation. These findings suggest USCs are a promising candidate for cell-based therapies due to their comparable immune-regulating capabilities to bone marrow mesenchymal stem cells.
Area of Science:
- Stem Cell Biology
- Immunology
- Regenerative Medicine
Background:
- Urine-derived stem cells (USCs) are a novel source for regenerative medicine.
- Their immunomodulatory characteristics require further investigation for therapeutic applications.
Purpose of the Study:
- To characterize the immunomodulatory properties of human USCs.
- To evaluate their potential in cell-based therapies.
Main Methods:
- Isolation and expansion of human USCs from urine samples.
- Flow cytometry for cell surface marker analysis.
- Mixed lymphocyte reaction (MLR) and NK cytotoxicity assays to assess immunomodulatory potential.
- Cytokine profiling using human cytokine proteome array.
Main Results:
- USCs exhibited a mesenchymal stem cell (MSC) phenotype.
- USCs significantly inhibited peripheral blood mononuclear cell (PBMNC) proliferation in MLR.
- Natural killer (NK) cells showed reduced cytotoxicity against USCs compared to other cell types.
- USCs secreted higher levels of immunomodulatory cytokines upon stimulation.
Conclusions:
- USCs possess significant immunomodulatory properties.
- They secrete immunoregulatory cytokines, comparable to bone marrow mesenchymal stem cells (BMSCs).
- USCs represent a promising cell source for immunotherapy.
Background:
Urine-derived stem cells (USCs) have been widely researched as a novel cell source for stem cell therapy, but their immunomodulatory characteristics remain to be investigated. This study aimed to characterize the immunomodulatory properties of human USCs.
Methods:
Human USCs were isolated from fresh voiding urine samples from healthy male donors and expanded. Their cell surface markers were characterized by flow cytometry analysis and the telomerase activities for several USCs clones were determined. The immunosuppressive potential of USCs was evaluated by the performing the mixed lymphocyte reaction (MLR) [co-culture with peripheral blood mononuclear cells (PBMNCs)] and natural killer cells (NK) cytotoxicity assay. USCs cytokines release profile was determined by using human cytokine proteome array.
Results:
USCs exhibited high cell surface expression of embryonic/mesenchymal stem cells (MSCs) markers CD29, CD44, CD54, CD73, CD90, CD146, and CD166, while lacked expression of hematopoietic stem cell markers CD11, CD14, CD19, CD31, CD34, CD45, B cell marker CD79, and co-stimulatory factors CD80 and CD86, thus, exhibiting the phenotype of MSCs. MLR indicated that USCs significantly inhibited the proliferation of PBMNCs, as compared to that of the human smooth muscle cells (SMCs). In cell cytotoxicity assays, NK cells displayed less cytotoxicity against USCs than against bone marrow mesenchymal stem cells (BMSCs) and SMCs. Furthermore, upon PBMNCs stimulation, USCs secreted higher levels of immunomodulatory cytokines, including IL-6, IL-8, MCP-1, RANTES, GROα, and GM-CSF, compared to those of BMSCs, especially when directly contact mix-culture with PBMNCs.
Conclusions:
USCs secreted immunoregulatory cytokines and possessed immunomodulatory properties, comparable to those of BMSCs.
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