Kasenda Benjamin, Kassmer Susannah H, Niggemann Bernd, Schiermeier Sven, Hatzmann Wolfgang, Zänker Kurt S, Dittmar Thomas
Institute of Immunology, Witten/Herdecke University, Witten, Germany.
Br J Haematol. 2008 Sep;142(5):831-5. doi: 10.1111/j.1365-2141.2008.07256.x. Epub 2008 Jun 5.
Addition of the inflammatory cytokine interleukin (IL)-6 to the culture medium of human cord blood haematopoietic stem and progenitor cells (HSPCs) has been shown to lead to an altered stromal cell-derived factor-1alpha-dependent migratory phenotype. This study investigated whether this effect was attributed to a differential engagement of protein kinase C (PKC) isotypes. The migratory activity of both Flt3-ligand and Flt3-ligand/IL-6 cultured cord blood HSPCs was PKC-alpha dependent on day 1, but PKC-alpha independent after 5 d of cultivation. PKC-alpha expression was not down-regulated in cells cultured for 5 d indicating a switch of signalling molecules directing cell migration.
已证明,在人脐带血造血干细胞和祖细胞(HSPCs)的培养基中添加炎性细胞因子白细胞介素(IL)-6会导致基质细胞衍生因子-1α依赖性迁移表型发生改变。本研究调查了这种效应是否归因于蛋白激酶C(PKC)同工型的不同参与。在培养第1天,Flt3配体和Flt3配体/IL-6培养的脐带血HSPCs的迁移活性均依赖PKC-α,但培养5天后则不依赖PKC-α。在培养5天的细胞中,PKC-α表达未下调,表明指导细胞迁移的信号分子发生了转换。