Lee Seung-Woo, Park Yunji, So Takanori, Kwon Byoung S, Cheroutre Hilde, Mittler Robert S, Croft Michael
Division of Molecular Immunology, La Jolla Institute for Allergy and Immunology, San Diego, California 92121, USA.
Nat Immunol. 2008 Aug;9(8):917-26. doi: 10.1038/ni.1632. Epub 2008 Jul 6.
The costimulatory molecule 4-1BB and its ligand 4-1BBL can control adaptive immunity, but here we show that their interaction also suppressed myelopoiesis. We found that 4-1BBL was expressed on hematopoietic stem cells, differentiating common myeloid progenitors and granulocyte-macrophage progenitors, and 4-1BB was inducible on activated myeloid progenitors. Steady-state numbers of granulocyte-macrophage progenitors, myeloid-lineage cells and mature dendritic cells were higher in 4-1BB- and 4-1BBL-deficient mice, indicative of a negative function, and we confirmed that result with bone marrow chimeras and in vitro, where the absence of interactions between 4-1BB and 4-1BBL led to enhanced differentiation into dendritic cell lineages. The regulatory activity was mediated by 4-1BBL, with binding by 4-1BB inhibiting differentiation of myeloid progenitors. Thus, 4-1BB and 4-1BBL have a previously unknown function in limiting myelopoiesis and the development of dendritic cells.
共刺激分子4-1BB及其配体4-1BBL可调控适应性免疫,但我们在此表明它们的相互作用也会抑制骨髓生成。我们发现4-1BBL在造血干细胞、分化中的普通髓系祖细胞和粒细胞-巨噬细胞祖细胞上表达,而4-1BB在活化的髓系祖细胞上可被诱导表达。在4-1BB和4-1BBL缺陷型小鼠中,粒细胞-巨噬细胞祖细胞、髓系谱系细胞和成熟树突状细胞的稳态数量更高,表明存在负向功能,并且我们通过骨髓嵌合体和体外实验证实了这一结果,在体外实验中,4-1BB与4-1BBL之间缺乏相互作用会导致向树突状细胞谱系的分化增强。这种调节活性由4-1BBL介导,4-1BB的结合会抑制髓系祖细胞的分化。因此,4-1BB和4-1BBL在限制骨髓生成和树突状细胞发育方面具有此前未知的功能。