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人外周血CD34+细胞来源嗜酸性粒细胞的生长与分化

Growth and differentiation of eosinophils from human peripheral blood CD 34+ cells.

作者信息

Shalit M

机构信息

Allergy and Immunology Unit, Hadassah Medical Center, Jerusalem, Israel.

出版信息

Allerg Immunol (Paris). 1997 Jan;29(1):7-10.

PMID:9025988
Abstract

Small numbers of CD34+ primitive hematopoietic progenitors are found in normal human peripheral blood. These cells differentiate to myeloid or lymphoid lineage under the influence of growth factors. We investigated the effects of IL5 and other growth factors on the production of eosinophils from peripheral blood CD34+ cells. CD34+ cells were plated in agarose with different combinations of cytokines. At 14 days of growth a triple stain technique was used to identify eosinophil, monocyte and neutrophil colonies. IL5 alone did not support colony growth. In contrast GM-CSF and IL3 alone or together supported the generation of more than 50% eosinophil colonies. Addition of IL5 increased the fraction of eosinophil colonies to over 70%. Under the best conditions (IL3 + GM-CSF + IL5), the addition of interferon-a or LPS inhibited colony growth by 51% and 58%, respectively. Since IL5 alone did not support colony growth from CD34+ cells, we determined when IL5 responsive cells appeared in culture. Cells were grown initially with IL3 + GM-CSF, washed, and plated with IL5 alone. Only when progenitors were grown at least 3 days, could IL5 serve as the single growth factor supporting pure eosinophil colony growth (47 colonies/104 cells plated at day 3 and 134 colonies/104 cells at day 7). Growth of CD34+ in liquid culture for 28 days in the presence of IL3, GM-CSF and IL5 resulted in almost 250 fold increase in cell number, yielding a population of 83% maturing eosinophils. We used our culture system and the sensitive technique of RT-PCR to analyze the kinetics of production of mRNA transcripts encoding several eosinophil proteins. Freshly isolated CD34+ cells contained no eosinophil granule protein transcripts and barely detectable amounts of some oxidase protein transcripts. At day 3 of culture no cells recognizable by histochemical staining as eosinophils could be detected, but transcripts for all five eosinophil granule proteins were present. These transcripts increased several fold during the entire culture period. Similar kinetics were seen for the NADPH oxidase protein transcripts. These studies demonstrate that within 3 days of culture, peripheral blood CD34+ cells can become committed to the eosinophil lineage as demonstrated by responsiveness to IL5 and production of specific protein transcripts.

摘要

在正常人外周血中可发现少量CD34+原始造血祖细胞。这些细胞在生长因子的影响下分化为髓系或淋巴系细胞。我们研究了白细胞介素5(IL5)和其他生长因子对人外周血CD34+细胞产生嗜酸性粒细胞的影响。将CD34+细胞接种于含有不同细胞因子组合的琼脂糖中。培养14天时,采用三重染色技术鉴定嗜酸性粒细胞、单核细胞和中性粒细胞集落。单独使用IL5不能支持集落生长。相反,单独使用粒细胞-巨噬细胞集落刺激因子(GM-CSF)或IL3或二者联合使用可支持生成超过50%的嗜酸性粒细胞集落。添加IL5可使嗜酸性粒细胞集落比例增加至70%以上。在最佳条件下(IL3 + GM-CSF + IL5),添加干扰素-α或脂多糖(LPS)可分别使集落生长抑制51%和58%。由于单独使用IL5不能支持CD34+细胞的集落生长,我们确定了培养中何时出现对IL5有反应的细胞。细胞最初用IL3 + GM-CSF培养,洗涤后,再单独用IL5接种。只有当祖细胞至少培养3天时,IL5才能作为支持纯嗜酸性粒细胞集落生长的单一生长因子(第3天接种的104个细胞中有47个集落,第7天有134个集落/104个细胞)。在IL3、GM-CSF和IL5存在的情况下,CD34+细胞在液体培养中培养28天,细胞数量增加了近250倍,产生了一个成熟嗜酸性粒细胞占83%的细胞群体。我们使用我们的培养系统和逆转录-聚合酶链反应(RT-PCR)敏感技术分析了几种嗜酸性粒细胞蛋白编码mRNA转录物的产生动力学。新鲜分离的CD34+细胞不含嗜酸性粒细胞颗粒蛋白转录物,某些氧化酶蛋白转录物的含量也几乎检测不到。在培养第3天时,通过组织化学染色无法检测到可识别为嗜酸性粒细胞的细胞,但所有五种嗜酸性粒细胞颗粒蛋白的转录物均存在。在整个培养期间,这些转录物增加了几倍。烟酰胺腺嘌呤二核苷酸磷酸(NADPH)氧化酶蛋白转录物也呈现类似的动力学。这些研究表明,在培养3天内,外周血CD34+细胞可如对IL5的反应性和特定蛋白转录物的产生所示,定向分化为嗜酸性粒细胞系。

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