Lee HakMo, Ratajczak Mariusz Z
James Graham Brown Cancer Center, Stem Cell Institute, University of Louisville, 500 Floyd St., Louisville, KY 40202, USA.
Arch Immunol Ther Exp (Warsz). 2009 Jul-Aug;57(4):269-78. doi: 10.1007/s00005-009-0037-6. Epub 2009 Jul 4.
The mobilization of hematopoietic stem/progenitor cells (HSPCs) from bone marrow into peripheral blood (PB) is still not fully understood. Different chemokines, cytokines, growth factors, and neurotransmitters have been described that facilitate this process. However, mounting evidence suggests that mobilization of HSPCs is a part of the immune response and is mediated by innate immunity. We discuss evidence showing that complement system cleavage fragments play a crucial role in both the retention and mobilization of HSPCs by modulating their responsiveness to stromal-derived growth factor-1 (SDF-1) gradient (by C3-derived anaphylatoxins) and by modulating the release of granulocytes into PB that subsequently facilitate the egress of HSPCs (by C5-derived anaphylatoxins).
造血干/祖细胞(HSPCs)从骨髓动员至外周血(PB)的机制仍未完全明确。已有多种趋化因子、细胞因子、生长因子及神经递质被报道可促进这一过程。然而,越来越多的证据表明,HSPCs的动员是免疫反应的一部分,且由固有免疫介导。我们讨论了相关证据,这些证据表明补体系统裂解片段在HSPCs的留存和动员过程中均发挥关键作用,其作用方式包括通过调节HSPCs对基质衍生生长因子-1(SDF-1)梯度的反应性(通过C3衍生的过敏毒素)以及调节粒细胞释放至外周血中,进而促进HSPCs的流出(通过C5衍生的过敏毒素)。