Gabbianelli M, Pelosi E, Montesoro E, Valtieri M, Luchetti L, Samoggia P, Vitelli L, Barberi T, Testa U, Lyman S
Department of Hematology-Oncology, Instituto Superiore di Sanità, Rome, Italy.
Blood. 1995 Sep 1;86(5):1661-70.
We have evaluated the effects of the flt3 receptor ligand (FL) on hematopoietic progenitors/stem cells (HPCs/HSCs) stringently purified from adult peripheral blood and grown in different culture systems. In these experiments HPCs/HSCs were treated with FL +/- kit ligand (KL) +/- monocyte colony-stimulatory factor (M-CSF). In clonogenetic HPC culture supplemented with interleukin-3 (IL-3)/granulomonocyte-CSF (GM-CSF)/erythropoietin (Epo), FL potentiates colony-forming unit (CFU)-GM proliferation in terms of colony number and size, but exerts little effect on burst-forming units-erythroid (BFU-E) and CFU-granulocyte erythroid megakaryocyte macrophage (CFU-GEMM) growth, whereas KL enhances the proliferation of all HPC types; combined FL+KL +/- M-CSF treatment causes a striking shift of CFU-GM colonies from granulocytic to monocytic differentiation. In liquid suspension HPC culture, FL alone induces differentiation along the monocytic and to a minor extent the basophilic lineages, whereas M-CSF alone stimulates prevalent monocytic differentiation but little cell proliferation: combined M-CSF+FL treatment causes both proliferation and almost exclusive monocytic differentiation (97% monocytes in fetal calf serum-rich (FCS+) culture conditions, mean value). At primitive HPC level, FL potentiates the clonogenetic capacity of colony-forming units-blast (CFU-B) and high proliferative potential colony-forming cells (HPP-CFC) in primary and secondary culture; KL exerts a similar action, and additive effects are induced by FL combined with KL. More important, addition of FL alone causes a significant amplification of the number of long-term culture-initiating cells (LTC-ICs), ie, putative repopulating HSCs, whereas this effect is not induced by KL. The FL effects correlate with flt3 mRNA expression in HPCs differentiating throught the erythroid or GM pathway in liquid suspension culture: (1) flt3 mRNA is expressed in freshly purified, resting HPCs; after growth factor stimulus the message (2) is abruptly down-modulated in HPC erythroid differentiation, but (3) is sustainedly expressed through HPC GM differentiation and abolished in GM precursor maturation. This pattern contrasts with the gradual downmodulation of c-kit through both erythroid and GM HPC differentiation. The results indicate that FL exerts a stimulatory action on primitive HPCs, including a unique expanding effect on putative stem cells, whereas its distal proliferative/differentiative action is largely restricted to CFU-GM and monocytic precursors. The latter effect is potentiated by KL and M-CSF, thus suggesting that the structural similarities of FL, KL, M-CSF, and their tyrosine kinase receptors may mediate positive interactions of these growth factors son monocytic differentiation.
我们评估了Flt3受体配体(FL)对从成人外周血中严格纯化并在不同培养系统中生长的造血祖细胞/干细胞(HPCs/HSCs)的影响。在这些实验中,HPCs/HSCs用FL±干细胞因子(KL)±单核细胞集落刺激因子(M-CSF)处理。在补充有白细胞介素-3(IL-3)/粒细胞-巨噬细胞集落刺激因子(GM-CSF)/促红细胞生成素(Epo)的克隆形成HPC培养中,FL在集落数量和大小方面增强了集落形成单位(CFU)-GM的增殖,但对红系爆式集落形成单位(BFU-E)和粒-红-巨核-巨噬细胞集落形成单位(CFU-GEMM)的生长影响很小,而KL增强了所有HPC类型的增殖;联合FL+KL±M-CSF处理导致CFU-GM集落从粒细胞分化向单核细胞分化发生显著转变。在液体悬浮HPC培养中,单独的FL诱导单核细胞系分化,并在较小程度上诱导嗜碱性细胞系分化,而单独的M-CSF刺激主要的单核细胞系分化,但细胞增殖很少:联合M-CSF+FL处理导致细胞增殖并几乎完全是单核细胞系分化(在富含胎牛血清(FCS+)的培养条件下,单核细胞平均值为97%)。在原始HPC水平,FL增强了集落形成单位- blast(CFU-B)和高增殖潜能集落形成细胞(HPP-CFC)在原代和传代培养中的克隆形成能力;KL发挥类似作用,FL与KL联合诱导相加效应。更重要的是,单独添加FL导致长期培养起始细胞(LTC-ICs)数量显著增加,即假定的再增殖HSCs,而KL不诱导这种效应。FL的作用与液体悬浮培养中通过红系或GM途径分化的HPCs中flt3 mRNA表达相关:(1)flt3 mRNA在新鲜纯化的静止HPCs中表达;生长因子刺激后,(2)该信息在HPC红系分化中突然下调,但(3)在HPC GM分化过程中持续表达,并在GM前体成熟时消失。这种模式与c-kit在红系和GM HPC分化过程中的逐渐下调形成对比。结果表明,FL对原始HPCs发挥刺激作用,包括对假定干细胞的独特扩增作用,而其远端增殖/分化作用在很大程度上仅限于CFU-GM和单核细胞前体。后一种作用被KL和M-CSF增强,因此表明FL、KL、M-CSF及其酪氨酸激酶受体的结构相似性可能介导这些生长因子在单核细胞分化中的正向相互作用。