Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice
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OriginalPaper|Updated:2021-08-27
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Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice
Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice
中国结合医学杂志(英文版)2013年19卷第5期 页码:360-366
Affiliations:
1. Research Institute of Hematopathy, the First Affiliated Hospital, Zhejiang Chinese Medical University,Hangzhou,China
2. Tongde Hospital of Zhejiang Province,Hangzhou,China
Author bio:
Funds:
Supported by Zhejiang Provincial Natural Science Foundation of China (No. Y207728 and No. Y2080036) and Traditional Chinese Medicine Administration Bureau of Zhejiang Province, China (No. 2008YA005)
Yin, Lm., Jiang, Hf., Wang, X. et al. Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice., Chin. J. Integr. Med. 19, 360–366 (2013). https://doi.org/10.1007/s11655-012-1210-z
Li-ming Yin, Hui-fang Jiang, Xiao Wang, et al. Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice[J]. Chinese Journal of Integrative Medicine, 2013,19(5):360-366.
Yin, Lm., Jiang, Hf., Wang, X. et al. Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice., Chin. J. Integr. Med. 19, 360–366 (2013). https://doi.org/10.1007/s11655-012-1210-zDOI:
Li-ming Yin, Hui-fang Jiang, Xiao Wang, et al. Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice[J]. Chinese Journal of Integrative Medicine, 2013,19(5):360-366. DOI: 10.1007/s11655-012-1210-z.
Effects of sodium copper chlorophyllin on mesenchymal stem cell function in aplastic anemia mice
摘要
To investigate the effects of sodium copper chlorophyllin (SCC) on the proliferation
differentiation and immunomodulatory function of mesenchymal stem cells (MSCs) from mice with aplastic anemia. A mouse model of aplastic anemia was established by exposure of BALB/c mice to sublethal doses of 5.0 Gy Co60 γ radiation
followed by transplantation of 2×106 lymph node cells from DBA/2 donor mice within 4 h after radiation. Aplastic anemic BALB/c mice were randomly divided into six groups: the treated groups
which received 25
50
or 100 mg/kg/day SCC
respectively; a positive control group treated with cyclosporine A (CsA); and an untreated model control group (model group); while
the non-irradiated mice as the normal control group. SCC or CsA were administered by gastrogavage for 20 days
starting on day 4 after irradiation. Peripheral blood cells were counted and colony-forming fibroblasts (CFU-F) in the bone marrow were assayed. The ability of MSCs to form calcium nodes after culture in osteoinductive medium was also observed. The immunosuppressive effect of MSCs on T lymphocytes was analyzed by enzyme-linked immunosorbent assay and flow cytometry
to evaluate the efficacy of SCC in mice with aplastic anemia. Peripheral blood white cell and platelet counts were increased by medium and high SCC doses
compared with the untreated control. CFU-Fs were also increased compared with the untreated control
and the numbers of calcium nodes in MSCs in osteoinductive medium were elevated in response to SCC treatment. The percentage of Forkhead box protein 3 (FOXP3+) T cells was increased in T cell-MSC cocultures
and the cytokine transforming growth factor β1 was up-regulated in SCC-treated groups. The results of this study suggest that SCC not only promotes the proliferation and differentiation of MSCs
but also improves their immunoregulatory capacity in mice with aplastic anemia.
Abstract
To investigate the effects of sodium copper chlorophyllin (SCC) on the proliferation
differentiation and immunomodulatory function of mesenchymal stem cells (MSCs) from mice with aplastic anemia. A mouse model of aplastic anemia was established by exposure of BALB/c mice to sublethal doses of 5.0 Gy Co60 γ radiation
followed by transplantation of 2×106 lymph node cells from DBA/2 donor mice within 4 h after radiation. Aplastic anemic BALB/c mice were randomly divided into six groups: the treated groups
which received 25
50
or 100 mg/kg/day SCC
respectively; a positive control group treated with cyclosporine A (CsA); and an untreated model control group (model group); while
the non-irradiated mice as the normal control group. SCC or CsA were administered by gastrogavage for 20 days
starting on day 4 after irradiation. Peripheral blood cells were counted and colony-forming fibroblasts (CFU-F) in the bone marrow were assayed. The ability of MSCs to form calcium nodes after culture in osteoinductive medium was also observed. The immunosuppressive effect of MSCs on T lymphocytes was analyzed by enzyme-linked immunosorbent assay and flow cytometry
to evaluate the efficacy of SCC in mice with aplastic anemia. Peripheral blood white cell and platelet counts were increased by medium and high SCC doses
compared with the untreated control. CFU-Fs were also increased compared with the untreated control
and the numbers of calcium nodes in MSCs in osteoinductive medium were elevated in response to SCC treatment. The percentage of Forkhead box protein 3 (FOXP3+) T cells was increased in T cell-MSC cocultures
and the cytokine transforming growth factor β1 was up-regulated in SCC-treated groups. The results of this study suggest that SCC not only promotes the proliferation and differentiation of MSCs
but also improves their immunoregulatory capacity in mice with aplastic anemia.
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相关机构
The Third People’s Hospital of Hangzhou
Department of Oncology, Zhejiang Provincial People’s Hospital
Institution of Hematology Research, The First Affiliated Hospital of Zhejiang Chinese Medical University