Title Adipose-Derived Mesenchymal Stem Cells (ADSCs) With the Potential to Ameliorate Platelet Recovery, Enhance Megakaryopoiesis, and Inhibit Apoptosis of Bone Marrow Cells in a Mouse Model of Radiation-Induced Thrombocytopenia
Authors Zhang, Jiamin
Zhou, Shiyuan
Zhou, Yi
Feng, Feier
Wang, Qianming
Zhu, Xiaolu
Zhao, Jingzhong
Fu, Haixia
Lv, Meng
Ai, Huisheng
Huang, Xiaojun
Zhang, Xiaohui
Affiliation Peking Univ, Inst Hematol, Peking Univ Peoples Hosp, 11 Xizhimen South St, Beijing 100871, Peoples R China.
Peking Univ Peoples Hosp, Dept Clin Lab, Beijing, Peoples R China.
Acad Mil Med Sci, Affiliated Hosp, Dept Hematol, Beijing, Peoples R China.
Keywords Adipose-derived mesenchymal stem cells (ADSCs)
Radiation
Thrombocytopenia
Megakaryocytopoiesis
Apoptosis
HEMATOPOIESIS IN-VITRO
REGENERATIVE MEDICINE
PROGENITOR CELLS
RHESUS-MONKEYS
THROMBOPOIETIN
VIVO
TISSUE
PATHWAY
INJURY
TRANSPLANTATION
Issue Date 2016
Publisher CELL TRANSPLANTATION
Citation CELL TRANSPLANTATION.2016,25,(2),261-273.
Abstract Substantial damage to the bone marrow can be caused by exposure to radiation, which can then develop into severe thrombocytopenia. In this study, we investigated the in vivo impact of adipose-derived mesenchymal stem cells (ADSCs) on megakaryopoiesis and platelet recovery in irradiated mice. Radiation markedly reduced peripheral blood counts. Recovery of both platelets and WBCs was better in the ADSC-treated group compared with the saline group and the fibroblast group 21 days after irradiation. A significant increase in the total CFU and MK-CFU after irradiation was observed in the ADSC group compared with the saline group and the fibroblast group. Further, the proportion of CD41(+) cells in the ADSC group was significantly higher than that in the saline group and the fibroblast group. ADSC treatment significantly improved the cellularity and decreased the apoptotic cells in the bone marrow while normal fibroblasts did not. Administration of ADSCs upregulated protein expression of phosphorylated Akt and Bcl-xL, whereas the expression of Bax, a protein related to apoptosis, was significantly lower in the ADSC group. In conclusion, this study suggests that ADSCs were capable of promoting platelet recovery, improving megakaryopoiesis, and inhibiting apoptosis of bone marrow cells in irradiated mice. The antiapoptotic effect of ADSCs is likely to be mediated via the PI3K/Akt pathway. These findings may provide a scientific basis for using ADSCs as a new therapy after irradiation.
URI http://hdl.handle.net/20.500.11897/436119
ISSN 0963-6897
DOI 10.3727/096368915X688155
Indexed SCI(E)
PubMed
Appears in Collections: 人民医院

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