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从CD34+祖细胞生成人树突状细胞并使其分化。

Growth and differentiation of human dendritic cells from CD34+ progenitors.

作者信息

Szabolcs P, Ciocon D H, Moore M A, Young J W

机构信息

Laboratory of Cellular Physiology and Immunology, Rockefeller University, New York, New York 10021, USA.

出版信息

Adv Exp Med Biol. 1997;417:15-9. doi: 10.1007/978-1-4757-9966-8_3.

DOI:10.1007/978-1-4757-9966-8_3
PMID:9286331
Abstract

Human dendritic cells can be generated from bone marrow CD34+ progenitors in the presence of GM-CSF and TNF alpha. The addition of a factor like c-kit-ligand optimizes the expansion of dendritic cells, as well as the other myeloid progeny grown under the same conditions, and facilitates their identification and characterization. In contrast to cord blood, where dendritic cells account for the majority of the class II MHC positive myeloid progeny, bone marrow CD34(+)-derived dendritic cells are less frequent than macrophages. When mature macrophages are depleted from days 5-6 cultures, terminally differentiated CD14+ HLA-DR dendritic cells as well as non-monocyte/macrophage CD14+ HLA-DR+ cells can be distinguished. The latter are post-CFU, bipotential, intermediate precursors that can terminally differentiate into either dendritic cells or macrophages depending on subsequent cytokine exposure. Human CD34+ progenitors isolated from bone marrow, as well as cord and peripheral blood, include CFU-DC that give rise to pure dendritic cell colonies in the combined presence of GM-CSF and TNF alpha. The different sources of CD34+ progenitors are not equivalent, however, with respect to frequency of CFU-DC growth. Cord blood is relatively enriched for dendritic cell progenitors. The developmental relationship of CFU-DC and CFU-GM, to the early developing dendritic cells and the bipotential intermediates observed in suspension culture, is not yet established.

摘要

在粒细胞-巨噬细胞集落刺激因子(GM-CSF)和肿瘤坏死因子α(TNFα)存在的情况下,人树突状细胞可由骨髓CD34+祖细胞生成。添加如c-kit配体这样的因子可优化树突状细胞的扩增,以及在相同条件下生长的其他髓系后代的扩增,并有助于它们的鉴定和表征。与脐带血不同,在脐带血中树突状细胞占II类主要组织相容性复合体(MHC)阳性髓系后代的大多数,而骨髓来源的CD34(+)树突状细胞比巨噬细胞少见。当从第5 - 6天的培养物中去除成熟巨噬细胞时,可区分出终末分化的CD14+ HLA-DR树突状细胞以及非单核细胞/巨噬细胞的CD14+ HLA-DR+细胞。后者是集落形成单位(CFU)后的双能中间前体细胞,根据随后的细胞因子暴露情况,可终末分化为树突状细胞或巨噬细胞。从骨髓以及脐带血和外周血中分离出的人CD34+祖细胞包括在GM-CSF和TNFα共同存在时可产生纯树突状细胞集落的CFU-DC(树突状细胞集落形成单位)。然而,就CFU-DC生长频率而言,不同来源的CD34+祖细胞并不等同。脐带血中树突状细胞祖细胞相对富集。CFU-DC和CFU-GM(粒细胞-巨噬细胞集落形成单位)与在悬浮培养中观察到的早期发育树突状细胞和双能中间体之间的发育关系尚未确定。

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Growth and differentiation of human dendritic cells from CD34+ progenitors.从CD34+祖细胞生成人树突状细胞并使其分化。
Adv Exp Med Biol. 1997;417:15-9. doi: 10.1007/978-1-4757-9966-8_3.
2
Identification of dendritic cell colony-forming units among normal human CD34+ bone marrow progenitors that are expanded by c-kit-ligand and yield pure dendritic cell colonies in the presence of granulocyte/macrophage colony-stimulating factor and tumor necrosis factor alpha.在正常人CD34+骨髓祖细胞中鉴定树突状细胞集落形成单位,这些祖细胞在c-kit配体作用下扩增,并在粒细胞/巨噬细胞集落刺激因子和肿瘤坏死因子α存在的情况下产生纯树突状细胞集落。
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Stem cell factor and FLT3-ligand are strictly required to sustain the long-term expansion of primitive CD34+DR- dendritic cell precursors.干细胞因子和FLT3配体是维持原始CD34+DR-树突状细胞前体长期扩增所必需的。
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Dendritic cells and macrophages can mature independently from a human bone marrow-derived, post-colony-forming unit intermediate.树突状细胞和巨噬细胞可从人骨髓来源的集落形成单位后中间细胞独立成熟。
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Expansion of immunostimulatory dendritic cells among the myeloid progeny of human CD34+ bone marrow precursors cultured with c-kit ligand, granulocyte-macrophage colony-stimulating factor, and TNF-alpha.在用人c-kit配体、粒细胞-巨噬细胞集落刺激因子和肿瘤坏死因子-α培养的人CD34+骨髓前体细胞的髓系后代中免疫刺激树突状细胞的扩增。
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Special susceptibility to apoptosis of CD1a+ dendritic cell precursors differentiating from cord blood CD34+ progenitors.从脐带血CD34 +祖细胞分化而来的CD1a +树突状细胞前体对细胞凋亡具有特殊易感性。
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Stem cell factor augments tumor necrosis factor-granulocyte-macrophage colony-stimulating factor-mediated dendritic cell hematopoiesis.干细胞因子增强肿瘤坏死因子-粒细胞巨噬细胞集落刺激因子介导的树突状细胞造血作用。
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CD34+ hematopoietic progenitors from human cord blood differentiate along two independent dendritic cell pathways in response to GM-CSF+TNF alpha.来自人脐带血的CD34+造血祖细胞在粒细胞-巨噬细胞集落刺激因子(GM-CSF)和肿瘤坏死因子α(TNFα)的作用下,沿着两条独立的树突状细胞途径分化。
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