Haig D M
Moredun Research Institute, Edinburgh, U.K.
J Comp Pathol. 1993 Oct;109(3):259-70. doi: 10.1016/s0021-9975(08)80251-4.
Conditions for the development of ovine bone marrow stromal cell-dependent LTBMC (long term bone marrow cultures) are described. After the addition of freshly isolated allogeneic bone marrow cells to a fully developed adherent stromal cell layer, myelopoiesis in the absence of erythropoiesis was sustained for up to 6 months. Macrophages and/or mast cells predominated in the later stages of all cultures. Stromal cell conditioned medium (SCM) and lymph node conditioned medium (LNCM) both support the development of a similar range of colony-forming cell (CFC) types in soft agar clonogenic assays, including multipotential-CFCs capable of development into more than two cell lineages, haemopoietic blast-CFCs (undifferentiated cells), mast-CFCs, macrophage-CFCs, eosinophil-CFCs and neutrophil-CFCs. However SCM supported the development of larger colonies containing more cells than those supported by LNCM. Furthermore SCM together with LNCM supported increased numbers of all colony types compared with the numbers supported by SCM or LNCM alone. In both liquid and semisolid agar cultures of bone marrow cells, SCM together with ovine interleukin-3 (IL-3) augmented the development of mast cells in particular, a cell type supported by IL-3 alone, whereas SCM together with ovine granulocyte-macrophage colony stimulating factor (GM-CSF) supported increased numbers of neutrophils and macrophages, which were cell types supported by GM-CSF alone. Bone marrow stromal cells and medium conditioned from these cells are therefore able to support myelopoiesis and the development of inflammatory cell types in culture. SCM in combination with IL-3 or GM-CSF is able to amplify the development of particular cell lineages supported by either IL-3 or GM-CSF alone.
本文描述了绵羊骨髓基质细胞依赖的长期骨髓培养(LTBMC)的培养条件。将新鲜分离的同种异体骨髓细胞添加到完全发育的贴壁基质细胞层后,在无红细胞生成的情况下,骨髓生成可持续长达6个月。在所有培养的后期阶段,巨噬细胞和/或肥大细胞占主导地位。在软琼脂克隆试验中,基质细胞条件培养基(SCM)和淋巴结条件培养基(LNCM)都支持一系列相似的集落形成细胞(CFC)类型的发育,包括能够发育成两种以上细胞谱系的多能CFC、造血母细胞CFC(未分化细胞)、肥大细胞CFC、巨噬细胞CFC、嗜酸性粒细胞CFC和中性粒细胞CFC。然而,SCM支持形成比LNCM支持的更大且包含更多细胞的集落。此外,与单独使用SCM或LNCM相比,SCM与LNCM共同支持所有集落类型的数量增加。在骨髓细胞的液体和半固体琼脂培养中,SCM与绵羊白细胞介素-3(IL-3)一起尤其增强了肥大细胞的发育,肥大细胞是一种仅由IL-3支持的细胞类型,而SCM与绵羊粒细胞-巨噬细胞集落刺激因子(GM-CSF)一起支持中性粒细胞和巨噬细胞数量增加,中性粒细胞和巨噬细胞是仅由GM-CSF支持的细胞类型。因此,骨髓基质细胞和由这些细胞产生的条件培养基能够在培养中支持骨髓生成和炎症细胞类型的发育。SCM与IL-3或GM-CSF联合能够放大仅由IL-3或GM-CSF单独支持的特定细胞谱系的发育。