Bron D, De Bruyn C, Lagneaux L, Tondreau T, Delforge A
Bull Mem Acad R Med Belg. 2002;157(1-2):135-45; discussion 145-6.
The haematopoietic stem cell (HSC) has been first described in the mouse and now identify in human as well. Exposed to a cocktail of growth factor, this HSC can self re-new and/or differentiate into the three lineages we have in the peripheral blood. These HSC are of major importance in the clinics since they can be used for some marrow (or stem cell) transplantation, and lead to the cure of a number of malignant and non malignant hemopathies. We have today three sources of HSC: the bone marrow, the mobilized peripheral blood stem cell and the cord blood. Bone marrow used to be the classical source of HSC after harvesting by aspirations in the iliac crest. However, this approach is now supplanted by the recovery of HSC in peripheral blood using a cell separation after four days of G-CSF administration. These are several advantages of this technique, but the most important one is the more rapid hematopoietic recovery after transplantation, reducing the risk of infection and transfusion. A recent source of HSC is the umbilical cord blood. At the moment of delivery, the cord blood is extremely enriched in HSC due to the migration of these cells from the liver to the bone marrow stroma, where they will persist after birth. We have learned that the marrow stroma display a major role in the regulation of hematopoiesis and the pathogenesis of several malignant hemopathies can be explained by disturbance in the function of stromal cell. We have particularly studied the patho-genesis of chronic lymphocytic leukaemia. We have also observed that a subpopulation of stromal cells, the mesenchymal cells are of major importance in the microenvironment. In addition, the plasticity of these cells is demonstrated in vitro and we have currently a research program investigating its differentiation in neural cells. All these observations bring new promises in the treatment of hemopathies but also in some other neurological degenerative diseases.
造血干细胞(HSC)最早在小鼠中被描述,现在在人类中也已被识别。暴露于一组生长因子中,这种造血干细胞可以自我更新和/或分化为我们外周血中的三种细胞谱系。这些造血干细胞在临床上至关重要,因为它们可用于一些骨髓(或干细胞)移植,并能治愈多种恶性和非恶性血液病。如今我们有三种造血干细胞来源:骨髓、动员的外周血干细胞和脐带血。骨髓曾经是通过髂嵴穿刺采集造血干细胞的经典来源。然而,这种方法现在已被在给予粒细胞集落刺激因子(G-CSF)四天后通过细胞分离从外周血中回收造血干细胞的方法所取代。这项技术有几个优点,但最重要的是移植后造血恢复更快,降低了感染和输血的风险。造血干细胞的一个最新来源是脐带血。在分娩时,由于这些细胞从肝脏迁移到骨髓基质,脐带血中富含造血干细胞,出生后它们会在骨髓基质中持续存在。我们已经了解到骨髓基质在造血调节中起主要作用,几种恶性血液病的发病机制可以通过基质细胞功能紊乱来解释。我们特别研究了慢性淋巴细胞白血病的发病机制。我们还观察到基质细胞的一个亚群,即间充质细胞在微环境中至关重要。此外,这些细胞的可塑性在体外得到了证实,我们目前有一个研究项目,研究其向神经细胞的分化。所有这些观察结果为血液病的治疗以及其他一些神经退行性疾病带来了新的希望。