Institute of Biotechnology 2, Forschungszentrum Jülich, 52425, Jülich GmbH, Germany.
Cytotechnology. 1999 Jul;30(1-3):227-34. doi: 10.1023/A:1008085932764.
The ex vivo expansion of hematopoietic progenitor cells is of great interest for a variety of clinical applications, e.g. bone marrow transplantation or gene therapy. Therefore it is of general interest to develop a culture system, able to mimic the in vivo hematopoesis, which is a prerequisite for long-term hematopoietic culture. Our approach was to modify a continuously perfused bioreactor for cultivation and expansion of human hematopoietic stem cells. Therefore we immobilized stromal cells (human primary stromal cells or the murine cell line M2-10B4) in porous glass carriers in a fixed bed reactor and cocultivated human hematopoietic progenitor cells for several weeks. After inoculation of mononuclear cells derived from umbilical cord blood or peripheral blood stem cells both adherent and non adherent cells were harvested and analyzed by flow cytometry and short-term colony assays. During cultivation there was a permanent production of progenitor cells and mature blood cells derived from the immobilized cells in the carriers. We could demonstrate the immobilization of hematopoietic progenitor cells of the myeloid system detectable in short-term colony assays. Additionally we could observe the expansion of very early progenitor cells (CFU-GEMM) up to 4.2-fold and later progenitor cells (CFU-GM and BFU-E) up to 7-fold and 1.8-fold, respectively.
体外扩增造血祖细胞对于各种临床应用非常重要,例如骨髓移植或基因治疗。因此,开发一种能够模拟体内造血的培养系统是长期造血培养的前提,这是普遍关注的问题。我们的方法是修改连续灌注生物反应器,以培养和扩增人类造血干细胞。为此,我们将基质细胞(人原代基质细胞或鼠细胞系 M2-10B4)固定在多孔玻璃载体中,在固定床反应器中共同培养人类造血祖细胞数周。在接种脐血或外周血干细胞的单核细胞后,我们收获贴壁和非贴壁细胞,并通过流式细胞术和短期集落分析进行分析。在培养过程中,载体中固定化的细胞会持续产生祖细胞和成熟血细胞。我们可以证明在短期集落试验中可以检测到骨髓系统的造血祖细胞的固定化。此外,我们还可以观察到非常早期的祖细胞(CFU-GEMM)扩增高达 4.2 倍,后期祖细胞(CFU-GM 和 BFU-E)扩增高达 7 倍和 1.8 倍。