Wang Hui, Madariaga Maria Lucia, Wang Shumei, Van Rooijen Nico, Oldenborg Per-Arne, Yang Yong-Guang
Transplantation Biology Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02129, USA.
Proc Natl Acad Sci U S A. 2007 Aug 21;104(34):13744-9. doi: 10.1073/pnas.0702881104. Epub 2007 Aug 15.
Macrophages recognize CD47 as a marker of "self" and phagocytose CD47(null) hematopoietic cells. Using CD47 chimera models, here, we show that the phagocytic activity of macrophages against CD47(null) hematopoietic cells is conferred by CD47 expression on nonhematopoietic cells, and this "education" process is hematopoietic cell-independent. Macrophages in the chimeras where nonhematopoietic cells express CD47 phagocytose CD47(null) cells, whereas those in the chimeras lacking CD47 on nonhematopoietic cells are tolerant to CD47(null) cells. However, macrophages in the latter chimeras retain phagocytic activity against CD47(null) RBCs, demonstrating a split macrophage tolerance to CD47(null) hematopoietic cells. The findings highlight the potential importance of nonhematopoietic cells in the regulation of macrophage function, and suggest a previously uncharacterized mechanism of macrophage tolerance.
巨噬细胞将CD47识别为“自身”标记,并吞噬CD47缺失的造血细胞。在此,我们使用CD47嵌合体模型表明,巨噬细胞对CD47缺失的造血细胞的吞噬活性是由非造血细胞上的CD47表达赋予的,并且这个“教育”过程不依赖于造血细胞。在非造血细胞表达CD47的嵌合体中,巨噬细胞会吞噬CD47缺失的细胞,而在非造血细胞上缺乏CD47的嵌合体中,巨噬细胞对CD47缺失的细胞具有耐受性。然而,后一种嵌合体中的巨噬细胞对CD47缺失的红细胞仍保留吞噬活性,这表明巨噬细胞对CD47缺失的造血细胞存在分裂耐受性。这些发现突出了非造血细胞在调节巨噬细胞功能方面的潜在重要性,并提示了一种以前未被描述的巨噬细胞耐受机制。