Effects of tumor necrosis factor-α on immunoregulatory activities of mesenchymal stem cells in vitro and in vivo.
- Author:
Yong-Qi WANG
1
;
Zhi-Yong LI
;
Xiao-Fang CAO
;
Heng-Xiang WANG
;
Zi-Kuan GUO
Author Information
1. Department of Hematoloyg, General Hospital of Chinese Air Force, Beijing, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Arthritis, Experimental;
metabolism;
pathology;
Cell Proliferation;
drug effects;
Cells, Cultured;
Humans;
Male;
Mesenchymal Stromal Cells;
cytology;
drug effects;
immunology;
NF-kappa B;
metabolism;
Rats;
Rats, Sprague-Dawley;
Rats, Wistar;
Tumor Necrosis Factor-alpha;
pharmacology
- From:
Journal of Experimental Hematology
2012;20(4):981-984
- CountryChina
- Language:Chinese
-
Abstract:
Mesenchymal stem cells (MSC) are characterized by their potent immuno-regulatory activity, however our previous data have shown that MSC have no therapeutic effects on collagen-induced arthritis (CIA). To further clarify the complexity, the effects of tumor necrosis factor-alpha (TNF-α) on the in vitro and in vivo immunoregulatory activity of MSC were investigated in this study, as TNF-α is recognized as the key factor in the development of rheumatoid arthritis. The nuclear translocation of the inflammation-associated factor NF-κB was observed after human umbilical cord MSC were treated with TNF-α and the cell proliferation status was assessed by MTT test. The inhibitory effects of MSC or TNF-α-treated MSC on the mixed lymphocyte reaction, in which Wistar rat spleen mononuclear cells were served as the responders and the splenocytes from SD rat spleens as the stimulators, were also determined by the MTT test. Further, the therapeutic potentials of MSC or TNF-α-treated MSC were observed in a Wistar rat CIA model. The results showed that NF-κB translocated into the nuclei promptly after TNF-α treatment, though TNF-α had little effect on the MSC proliferation. MSC, whether pre-stimulated by TNF-α or not and when different doses were tested, exhibited obviously inhibitory effects on the proliferation of the lymphocytes (P < 0.001 for all groups tested), while MSC-treated by TNF-α displayed more potent suppression especially when low-density were used. Unexpectedly, the infiltration of inflammatory cells into the involved knees was aggravated by cell treatment and the pathological scores were significantly higher than those of controls (P < 0.05). It is concluded that the TNF-α exhibits different effects on immune regulation activity of MSC, and its underlying mechanism needs to further investigate.
