Preliminary establishment of transplanted human chronic myeloid leukemia model in nude mice.
- Author:
Xian-Min LI
1
;
Xin DING
;
Long-Zhen ZHANG
;
Jian-Nong CEN
;
Zi-Xing CHEN
Author Information
1. Suzhou University First Hospital, Jiangsu Institute of Hematology, Suzhou, Jiangsu Province, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Disease Models, Animal;
Humans;
Leukemia, Myelogenous, Chronic, BCR-ABL Positive;
Male;
Mice;
Mice, Nude;
Mice, SCID;
Neoplasm Transplantation;
Neoplastic Stem Cells;
Transplantation, Heterologous
- From:
Journal of Experimental Hematology
2011;19(6):1378-1382
- CountryChina
- Language:Chinese
-
Abstract:
Chronic myeloid leukemia (CML) is a malignant clonal disease derived from hematopoietic stem cells. CML stem cells were thought to be the root which could lead disease development and ultimately rapid change. However, a stable animal model for studying the characteristics of CML stem cells is currently lacking. This study was aimed to establish a transplanted human CML nude-mice model to further explore the biological behavior of CML stem cells in vivo, and to enrich CML stem cells in nude mice by series transplantation. The 4 - 6 weeks old BALB/c nude mice pretreated by splenectomy (S), cytoxan intraperitoneal injection (C) and sublethal irradiation (I) were transplanted intravenously with (5 - 7) × 10(7) of bone marrow mononuclear cells from CML patients in chronic phase. Alternatively, 4 - 6 weeks old BALB/c nude mice pretreated by lethal irradiation were transplanted intravenously with 5 × 10(6) homologous bone marrow cells of BALB/c nude mice together with (5 - 7) × 10(7) of bone marrow mononuclear cells from CML patients in chronic phase simultaneously. The leukemic cells engrafted and infiltrated in organs and bone marrow of the mice were tracked by reverse transcription-polymerase chain reaction (RT-PCR), plastic-embedded biopsy and flow cytometry. The results of these two methods were compared. The results showed that human CML cells engrafted and infiltrating into the bone marrow of two nude mice pretreated with SCI could be detected. In spite of the low successful rate, results suggested the feasibility of this method by using BALB/c nude mice as a human CML animal model. In contrast, in nude mice pretreated by the lethal dose irradiation, CML cells in the bone marrow could not be found. It is concluded that human bone marrow CML cells can results in leukemia in nude mice pretreated by SCI. Thus this study provides a new strategy for establishment of CML animal models which deserves further elaboration.
