Wognum A W, Visser T P, de Jong M O, Egeland T, Wagemaker G
Department of Hematology, Erasmus Universiteit, Rotterdam, The Netherlands.
Blood. 1995 Jul 15;86(2):581-91.
The target cell specificity of interleukin-3 (IL-3) was examined by flow cytometric analysis of IL-3 receptor (IL-3R) expression on rhesus monkey bone marrow (BM) cells using biotinylated IL-3. Only 2% to 5% of unfractionated cells stained specifically with the biotinylated IL-3 and most of these cells were present within the CD34+ subset. IL-3Rs were detected on small CD34dull/RhLA-DRbright/CD10+/CD27+/CD2-/++ +CD20- cells, which probably represent B-cell precursors. IL-3R+ CD34- BM cells, which were detected at low frequencies, consisted of small CD20dull/surface-IgM+/RhLA-DR+ cells. These cells represented immature B lymphocytes, whereas CD20bright mature B cells were IL-3R-. The highest IL-3R levels were detected on CD34dull/RhLA-DRbright blast-like cells. These cells differentiated into monocytes, neutrophils, and basophils after IL-3 and/or granulocyte-macrophage colony-stimulating factor (GM-CSF) stimulation in vitro. The CD34bright/IL-3R- subset contained all clonogenic erythroid and myeloid progenitors (burst-forming unit-erythroid and colony-forming unit-culture), whereas CD34bright/IL-3Rdull cells differentiated into monocytes, neutrophils, and erythroid cells after shorter culture periods. This finding showed that IL-3R expression increases during monocyte and granulocyte differentiation. Results of three-color experiments indicated that IL-3Rs are expressed on CD34bright/RhLA-DRbright cells as well as on CD34bright/RhLA-DRdull cells, with the latter population expression approximately twofold to threefold lower IL-3R levels. A large fraction (> 30%) of single-cell/well-sorted CD34bright/RhLA-DRdull cells formed multilineage colonies after 2 to 4 weeks of stimulation with IL-3, GM-CSF, Kit ligand, and IL-6. Individual colonies contained cells that still expressed CD34 as well as differentiated monocytes, granulocytes, and erythroid cells. These results confirmed that the CD34bright/RhLA-DRdull subset was enriched for immature, multipotent progenitor cells, whereas the CD34bright/RhLA-DRbright population mainly contained lineage-committed precursors. The results are consistent with the concept that IL-3Rs are induced at very early stages of hematopoiesis, as identified by high expression of CD34 and low expression of RhLA-DR. IL-3R expression continues to be low during differentiation into lineage-committed progenitors; gradually increases on differentiating progenitor cells for B cells, granulocytes, monocytes, and, possibly also, erythrocytes; but finally declines to undetectable levels during terminal differentiation into mature cells of all lineages in peripheral blood, with the exception of basophils.(ABSTRACT TRUNCATED AT 400 WORDS)
利用生物素化的白细胞介素-3(IL-3),通过流式细胞术分析恒河猴骨髓(BM)细胞上IL-3受体(IL-3R)的表达,来检测IL-3的靶细胞特异性。未分离的细胞中只有2%至5%能被生物素化的IL-3特异性染色,且这些细胞大多存在于CD34+亚群中。在小的CD34暗淡/RhLA-DR明亮/CD10+/CD27+/CD2- /++ +CD20-细胞上检测到IL-3R,这些细胞可能代表B细胞前体。低频检测到的IL-3R+ CD34- BM细胞由小的CD20暗淡/表面-IgM+/RhLA-DR+细胞组成。这些细胞代表未成熟的B淋巴细胞,而CD20明亮的成熟B细胞是IL-3R- 。在CD34暗淡/RhLA-DR明亮的母细胞样细胞上检测到最高水平的IL-3R。这些细胞在体外经IL-3和/或粒细胞-巨噬细胞集落刺激因子(GM-CSF)刺激后可分化为单核细胞、中性粒细胞和嗜碱性粒细胞。CD34明亮/IL-3R-亚群包含所有克隆性红系和髓系祖细胞(爆式红系集落形成单位和集落形成单位-培养),而CD34明亮/IL-3R暗淡细胞在较短培养期后可分化为单核细胞、中性粒细胞和红细胞。这一发现表明,IL-3R表达在单核细胞和粒细胞分化过程中增加。三色实验结果表明,IL-3R在CD34明亮/RhLA-DR明亮细胞以及CD34明亮/RhLA-DR暗淡细胞上均有表达,后者群体的IL-3R水平约低两到三倍。在经IL-3、GM-CSF、Kit配体和IL-6刺激2至4周后,大部分(>30%)单细胞/单孔分选的CD34明亮/RhLA-DR暗淡细胞形成多谱系集落。单个集落包含仍表达CD34的细胞以及分化的单核细胞、粒细胞和红细胞。这些结果证实,CD34明亮/RhLA-DR暗淡亚群富含未成熟的多能祖细胞,而CD34明亮/RhLA-DR明亮群体主要包含定向谱系前体。这些结果与如下概念一致,即IL-3R在造血的非常早期阶段被诱导,这可通过CD34的高表达和RhLA-DR的低表达来确定。在分化为定向谱系祖细胞的过程中,IL-3R表达持续较低;在分化为B细胞、粒细胞、单核细胞以及可能还有红细胞的祖细胞时逐渐增加;但最终在终末分化为外周血中所有谱系的成熟细胞(嗜碱性粒细胞除外)过程中降至不可检测水平。(摘要截短于400字)