| Literature DB >> 33386593 |
Masaki Iwasa1,2, Sumie Fujii3,4, Aya Fujishiro3,5, Taira Maekawa3, Akira Andoh5, Akifumi Takaori-Kondo4, Tatsuo Ichinohe6, Yasuo Miura3,4,6.
Abstract
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.Entities:
Keywords: Bone; Bone marrow mesenchymal stromal/stem cell; Complications; Hematopoiesis; Total body irradiation
Year: 2021 PMID: 33386593 DOI: 10.1007/s12185-020-03072-9
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490