Visser J W, Rozemuller H, de Jong M O, Belyavsky A
Institute of Applied Radiobiology and Immunology TNO, Rijswijk, The Netherlands.
Stem Cells. 1993 Jul;11 Suppl 2:49-55. doi: 10.1002/stem.5530110809.
Sorted fractions from mouse bone marrow containing highly purified hemopoietic stem and progenitor cells were studied for the expression of growth factor receptors. With the use of rhodamine 123 WGA+, 15-1.1-, low density cells were separated into quiescent pluripotent stem cells and committed progenitor cells. RNA was extracted and cDNA was prepared by reverse transcription. Using primers specific for growth factor receptors, the cDNA of each sorted fraction was amplified by polymerase chain reaction (PCR). The quiescent rhodamine 123 dull stem cell fraction was found to express the interleukin 3 (IL-3) receptor beta unit and c-kit, but not the granulocyte-macrophage colony stimulating factor (GM-CSF) receptor beta unit nor flk-2. The rhodamine 123 bright fraction with activated stem cells and mostly committed progenitor cells similarly expressed the IL-3-R beta, and c-kit. However, this fraction also expressed flk-2 and GM-CSF-R beta. Since the expression of c-kit in the stem cell fraction does not correspond with the poor response to the kit-ligand stem cell factor (SCF) by these cells, we further analyzed the fractions with respect to their binding of biotinylated SCF. The SCF-binding cells were found to be all rhodamine 123 bright. This indicates that the expression of c-kit is not sufficient to yield a functional receptor for SCF; c-kit probably needs a partner molecule to form a functional high-affinity binding site for SCF. Similar to the beta unit of the GM-CSF receptor, this partner is then not expressed in the stem cell fraction.(ABSTRACT TRUNCATED AT 250 WORDS)
对从小鼠骨髓中分离出的含有高度纯化造血干细胞和祖细胞的组分进行了生长因子受体表达的研究。利用罗丹明123 WGA +,将低密度细胞分离为静止的多能干细胞和定向祖细胞。提取RNA并通过逆转录制备cDNA。使用针对生长因子受体的特异性引物,通过聚合酶链反应(PCR)扩增每个分选组分的cDNA。发现静止的罗丹明123暗淡干细胞组分表达白细胞介素3(IL-3)受体β亚基和c-kit,但不表达粒细胞-巨噬细胞集落刺激因子(GM-CSF)受体β亚基和flk-2。含有活化干细胞和大多为定向祖细胞的罗丹明123明亮组分同样表达IL-3-Rβ和c-kit。然而,该组分也表达flk-2和GM-CSF-Rβ。由于干细胞组分中c-kit的表达与这些细胞对c-kit配体干细胞因子(SCF)的不良反应不相符,我们进一步分析了这些组分与生物素化SCF的结合情况。发现与SCF结合的细胞均为罗丹明123明亮细胞。这表明c-kit的表达不足以产生功能性的SCF受体;c-kit可能需要一个伴侣分子来形成功能性的高亲和力SCF结合位点。与GM-CSF受体的β亚基类似,该伴侣分子在干细胞组分中不表达。(摘要截短于250字)