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Stem Cells and Development
Phenotypic and Functional Comparison of Mesenchymal Stem Cells Derived from the Bone Marrow of Normal Adults and Patients with Hematologic Malignant Diseases

To cite this article:
Zhi-Gang Zhao, Yan Liang, Kai Li, Wei-Ming Li, Qiu-Bai Li, Zhi-Chao Chen, Ping Zou. Stem Cells and Development. August 2007, 16(4): 637-648. doi:10.1089/scd.2007.0008.

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Zhi-Gang Zhao 
Department of Hematology, Oncology Hospital of Tianjin Medical University, Tianjin, China.
Yan Liang 
Department of Hematology, Oncology Hospital of Tianjin Medical University, Tianjin, China.
Kai Li 
Department of Hematology, Oncology Hospital of Tianjin Medical University, Tianjin, China.
Wei-Ming Li 
Department of Hematology, Institute of Hematology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
Qiu-Bai Li 
Department of Hematology, Institute of Hematology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
Zhi-Chao Chen 
Department of Hematology, Institute of Hematology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
Ping Zou 
Department of Hematology, Institute of Hematology, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.

Mesenchymal stem cells (MSCs) have received much attention for their ability to differentiate into various cell types under specific conditions and to support the proliferation of hematopoietic stem cells. However, it is unclear whether the characteristics of MSCs are altered in different disease states. In this study, we obtained and expanded MSCs from bone marrow of patients with acute lymphoblastic leukemia (ALL), Hodgkin disease (HD), and non-Hodgkin lymphoma (NHL). Our results showed that MSCs derived from ALL, HD, and NHL were similar to normal adult bone marrow-derived MSCs in morphology, growth properties, surface epitopes, and differentiation ability in vitro. Moreover, MSCs derived from ALL, NHL, and HD had a normal karyotype and ultrastructure. These cells could express hematopoietic cytokines and support hematopoiesis in long-term culture. However, adherent cells isolated from bone marrow of patients with acute myeloid leukemia (AML) showed abnormal biological properties, including heterogeneity in morphology, limited proliferation capacity, and impaired differentiation and hematopoiesis support ability. These results indicate that there are differences in the characteristics of adherent cells derived from different disease states, which may be important for reasonable MSC selection in stem cell-based therapy.

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