Impact of 2 Gy γ-irradiation on the hallmark characteristics of human bone marrow-derived MSCs

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作者
Masaki Iwasa
Sumie Fujii
Aya Fujishiro
Taira Maekawa
Akira Andoh
Akifumi Takaori-Kondo
Tatsuo Ichinohe
Yasuo Miura
机构
[1] Kyoto University Hospital,Department of Transfusion Medicine and Cell Therapy
[2] Shiga University of Medical Science,Division of Gastroenterology and Hematology, Department of Medicine
[3] Kyoto University Graduate School for Medicine,Department of Hematology/Oncology
[4] Hiroshima University,Department of Hematology and Oncology, Research Institute for Radiation Biology and Medicine
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Bone marrow mesenchymal stromal/stem cell; Total body irradiation; Complications; Hematopoiesis; Bone;
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摘要
Two gray γ-irradiation is a widely employed basic module for total body irradiation (TBI) in allogeneic hematopoietic cell transplantation (HCT). The effects of γ-irradiation on hematopoietic and immune cells have been well investigated, but its effects on the bone marrow microenvironment (BMM) are unknown. Given the crucial contribution of mesenchymal/stromal stem cells (MSCs) in the BMM to hematopoiesis and osteogenesis, we investigated whether γ-irradiation affects the hallmark characteristics of human bone marrow-derived MSCs (BM-MSCs). Expansion of 2 Gy γ-irradiated BM-MSCs was delayed but eventually recovered. Colony formation and osteogenic, adipogenic, and chondrogenic differentiation capabilities of these cells were extensively suppressed. Irradiation of BM-MSCs did not affect the expansion of CD34 + hematopoietic stem and progenitor cells or production of CD11b + mature myeloid cells in co-cultures. However, it reduced production of CD19 + B-cells, as well as expression of CXCL12 and interleukin-7, which are essential for B-cell lymphopoiesis, in 2 Gy γ-irradiated BM-MSCs. Collectively, colony formation, osteogenic differentiation, and B-cell lymphopoiesis-supportive capabilities of γ-irradiated BM-MSCs were reduced. These effects may predispose survivors receiving HCT with TBI to defective bone formation and a perturbed humoral immune response.
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页码:703 / 711
页数:8
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