Radioprotection of Bone Marrow Hematopoiesis by CpG-oligodeoxynucleotides Administered to Mice after Total-body Irradiation
Author(s) -
Chao Zhang,
Jing Lin,
Jianguo Cui,
Bailong Li,
Cong Liu,
Jichao Wang,
Fu Gao,
Jianming Cai
Publication year - 2011
Publication title -
journal of radiation research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.643
H-Index - 60
eISSN - 1349-9157
pISSN - 0449-3060
DOI - 10.1269/jrr.10098
Subject(s) - bone marrow , cpg oligodeoxynucleotide , haematopoiesis , total body irradiation , white blood cell , spleen , immune system , immunology , cpg site , progenitor cell , medicine , stem cell , cancer research , chemistry , biology , chemotherapy , microbiology and biotechnology , biochemistry , gene expression , dna methylation , gene , cyclophosphamide
CpG-oligodeoxynucleotide (ODN), a synthetic analog of bacteria DNA, has attracted attention because it activates cells of an adaptive immune system and the innate immune system. In this study, we investigated whether CpG-ODN has radioprotective effects, when administered after total-body irradiation (TBI). Mice were treated with 50 µg CpG-ODN via intraperitoneal injection (i.p) within 30 min, 24 h and 48 h after TBI. Our results showed that the survival rate was enhanced at various levels of TBI. The calculated dose reduction factor (DRF) was 1.2. Bone marrow cell count and bone marrow histological examination indicated that CpG-ODN minimized the bone marrow damage induced by TBI. The data of the white blood cell (WBC) count, exogenous (CFU-S) and endogenous (endoCFU-S) colony forming unit-spleen count demonstrated that CpG-ODN reduced primitive hematopoietic stem cells damage and reconstituted hematopoiesis after TBI. Thus, we suggested that CpG-ODN had the potential to contribute to the improvement of the survival rate and limitation of myelosuppression induced by TBI.
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