Shezen E, Goldman R
Int J Cell Cloning. 1985 Mar;3(2):65-80. doi: 10.1002/stem.5530030201.
1,25-Dihydroxyvitamin D3 (1,25(OH)2D3) exerts a differential inhibitory effect on the formation of granulocyte, granulocyte/macrophage, and macrophage colonies grown from mouse bone marrow precursor cells; 50% inhibition was attained at 1.1, 2.3, and 23 nM 1,25(OH)2D3, respectively. The inhibition of colony formation, as well as phagocyte proliferation in liquid cultures, requires the presence of 1,25(OH)2D3 in the early stages of culture (up to 72 h after culture initiation). 1,25(OH)2D3 induces a dose- and time-dependent augmentation of the phagocytic capability of mononuclear phagocytes (up to 100%) towards both heat-killed yeast cells and IgG-coated sheep red blood cells. The augmentation of the phagocytic capability of the mononuclear phagocytes depends critically on when 1,25(OH)2D3 is added. It is effective when added up to 72 h after culture initiation, while at later stages (greater than or equal to 96 h) the cells are no longer induced to express enhanced phagocytic capability. We suggest that these phenomena may be relevant to hemopoietic processes.
1,25 - 二羟基维生素D3(1,25(OH)2D3)对从小鼠骨髓前体细胞生长而来的粒细胞、粒细胞/巨噬细胞和巨噬细胞集落的形成具有不同的抑制作用;在1.1、2.3和23 nM的1,25(OH)2D3浓度下,分别达到50%的抑制率。集落形成的抑制以及液体培养中吞噬细胞的增殖,需要在培养早期(培养开始后长达72小时)存在1,25(OH)2D3。1,25(OH)2D3诱导单核吞噬细胞对热灭活酵母细胞和IgG包被的绵羊红细胞的吞噬能力呈剂量和时间依赖性增强(高达100%)。单核吞噬细胞吞噬能力的增强关键取决于1,25(OH)2D3添加的时间。在培养开始后长达72小时添加时有效,而在后期(大于或等于96小时),细胞不再被诱导表达增强的吞噬能力。我们认为这些现象可能与造血过程相关。