Jo Deog-Yeon, Hwang Jin-Hee, Kim Jin-Man, Yun Hwan-Jung, Kim Samyong
Division of Hematology/Oncology, Department of Internal Medicine, and Department of Pathology, College of Medicine, Chungnam National University, Daejon, Korea.
Br J Haematol. 2003 May;121(4):649-52. doi: 10.1046/j.1365-2141.2003.04326.x.
This study investigated human bone marrow endothelial cells (BMEC) chemoattractive activity in relation to haematopoietic cell trafficking. BMEC-conditioned medium induced chemoattraction of haematopoietic progenitor cells. Migration was not inhibited by pretreating the cells with pertussis toxin (PTX) or 12G5, indicating that the chemoattractive activity was not dependent on stromal-cell-derived factor-1 (SDF-1). Spontaneous migration, but not SDF-1-mediated chemotaxis of haematopoietic progenitors, was better supported by BMEC as compared with umbilical vein endothelial cells. The superior migration was abolished by pretreating the cells with PTX, indicating that BMEC-derived SDF-1 favours bone marrow endothelium, with better transmigration of haematopoietic progenitors.
本研究调查了人类骨髓内皮细胞(BMEC)与造血细胞迁移相关的趋化活性。BMEC条件培养基可诱导造血祖细胞的趋化作用。用百日咳毒素(PTX)或12G5预处理细胞后,迁移并未受到抑制,这表明趋化活性不依赖于基质细胞衍生因子-1(SDF-1)。与脐静脉内皮细胞相比,BMEC对造血祖细胞的自发迁移(而非SDF-1介导的趋化作用)具有更好的支持作用。用PTX预处理细胞可消除这种优越的迁移能力,这表明BMEC衍生的SDF-1有利于骨髓内皮,使造血祖细胞具有更好的迁移能力。