Strobl Herbert
Institute of Immunology, University of Vienna, Vienna, Austria.
Int Arch Allergy Immunol. 2003 Jun;131(2):73-9. doi: 10.1159/000070921.
In vitro differentiation models of human CD34+ hematopoietic progenitor/stem cells have contributed significantly to our current understanding of dendritic cell (DC) development. DC sublineages seem to arise from common progenitors with monocytic cells. These progenitors seem to respond to instructive signals from cytokine receptors and steroids to follow defined sublineage differentiation pathways. Transcriptional processes involved in the regulation of lineage fate decisions of putative common DC progenitors remain poorly defined, as is our knowledge of the identities of DC precursors in vivo. Most likely, tissue-specific microenvironmental signals, including tumor-derived signals, critically modulate DC phenotype and function in vivo.
人CD34+造血祖细胞/干细胞的体外分化模型对我们目前对树突状细胞(DC)发育的理解有显著贡献。DC亚系似乎起源于与单核细胞共同的祖细胞。这些祖细胞似乎对细胞因子受体和类固醇发出的指导性信号作出反应,以遵循特定的亚系分化途径。参与假定的共同DC祖细胞谱系命运决定调控的转录过程仍不清楚,我们对体内DC前体的身份了解也同样有限。很可能,包括肿瘤衍生信号在内的组织特异性微环境信号在体内关键地调节DC表型和功能。