作者: Paik Wah Chow , Zariyantey Abdul Hamid , Kok Meng Chan , Salmaan Hussain Inayat-Hussain , Nor Fadilah Rajab
DOI: 10.1016/J.TAAP.2015.01.016
关键词:
摘要: Abstract Hematopoietic stem cells (HSCs) and hematopoietic progenitor (HPCs) are sensitive targets for benzene-induced hematotoxicity leukemogenesis. The impact of benzene exposure on the complex microenvironment HSCs HPCs remains elusive. This study aims to investigate mechanism linking targeting using phenotypic clonogenic analyses. Mouse bone marrow (BM) were exposed ex vivo metabolite, 1,4-benzoquinone (1,4-BQ), 24 h. Expression cellular surface antigens HSC (Sca-1), myeloid (Gr-1, CD11b), lymphoid (CD45, CD3e) populations confirmed by flow cytometry. clonogenicity was studied colony-forming unit (CFU) assay multilineage (CFU-GM CFU-GEMM) single-lineage (CFU-E, BFU-E, CFU-G, CFU-M) progenitors. 1,4-BQ demonstrated concentration-dependent cytotoxicity in mouse BM cells. percentage apoptotic increased (p