Paschall Amy V, Zhang Ruihua, Qi Chen-Feng, Bardhan Kankana, Peng Liang, Lu Geming, Yang Jianjun, Merad Miriam, McGaha Tracy, Zhou Gang, Mellor Andrew, Abrams Scott I, Morse Herbert C, Ozato Keiko, Xiong Huabao, Liu Kebin
Department of Biochemistry and Molecular Biology, Medical College of Georgia, Georgia Regents University, Augusta, GA 30912; Cancer Immunology, Inflammation and Tolerance Program, Cancer Center, Georgia Regents University, Augusta, GA 30912; Charlie Norwood VA Medical Center, Augusta, GA 30904;
Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029;
J Immunol. 2015 Mar 1;194(5):2369-79. doi: 10.4049/jimmunol.1402412. Epub 2015 Feb 2.
During hematopoiesis, hematopoietic stem cells constantly differentiate into granulocytes and macrophages via a distinct differentiation program that is tightly controlled by myeloid lineage-specific transcription factors. Mice with a null mutation of IFN regulatory factor 8 (IRF8) accumulate CD11b(+)Gr1(+) myeloid cells that phenotypically and functionally resemble tumor-induced myeloid-derived suppressor cells (MDSCs), indicating an essential role of IRF8 in myeloid cell lineage differentiation. However, IRF8 is expressed in various types of immune cells, and whether IRF8 functions intrinsically or extrinsically in regulation of myeloid cell lineage differentiation is not fully understood. In this study, we report an intriguing finding that, although IRF8-deficient mice exhibit deregulated myeloid cell differentiation and resultant accumulation of CD11b(+)Gr1(+) MDSCs, surprisingly, mice with IRF8 deficiency only in myeloid cells exhibit no abnormal myeloid cell lineage differentiation. Instead, mice with IRF8 deficiency only in T cells exhibited deregulated myeloid cell differentiation and MDSC accumulation. We further demonstrated that IRF8-deficient T cells exhibit elevated GM-CSF expression and secretion. Treatment of mice with GM-CSF increased MDSC accumulation, and adoptive transfer of IRF8-deficient T cells, but not GM-CSF-deficient T cells, increased MDSC accumulation in the recipient chimeric mice. Moreover, overexpression of IRF8 decreased GM-CSF expression in T cells. Our data determine that, in addition to its intrinsic function as an apoptosis regulator in myeloid cells, IRF8 also acts extrinsically to repress GM-CSF expression in T cells to control myeloid cell lineage differentiation, revealing a novel mechanism that the adaptive immune component of the immune system regulates the innate immune cell myelopoiesis in vivo.
在造血过程中,造血干细胞通过一个由髓系谱系特异性转录因子严格控制的独特分化程序,不断分化为粒细胞和巨噬细胞。干扰素调节因子8(IRF8)基因敲除的小鼠会积累CD11b(+)Gr1(+)髓系细胞,这些细胞在表型和功能上类似于肿瘤诱导的髓系来源抑制细胞(MDSC),这表明IRF8在髓系细胞谱系分化中起重要作用。然而,IRF8在多种免疫细胞中表达,IRF8在髓系细胞谱系分化调控中是内在发挥作用还是外在发挥作用尚未完全明确。在本研究中,我们报告了一个有趣的发现:尽管IRF8缺陷小鼠表现出髓系细胞分化失调以及由此导致的CD11b(+)Gr1(+) MDSC积累,但令人惊讶的是,仅在髓系细胞中缺乏IRF8的小鼠并未表现出异常的髓系细胞谱系分化。相反,仅在T细胞中缺乏IRF8的小鼠表现出髓系细胞分化失调和MDSC积累。我们进一步证明,IRF8缺陷的T细胞表现出GM-CSF表达和分泌升高。用GM-CSF处理小鼠会增加MDSC积累,过继转移IRF8缺陷的T细胞(而非GM-CSF缺陷的T细胞)会增加受体嵌合小鼠中的MDSC积累。此外, IRF8的过表达降低了T细胞中GM-CSF的表达。我们的数据表明,除了作为髓系细胞凋亡调节因子的内在功能外,IRF8还通过外在作用抑制T细胞中GM-CSF的表达来控制髓系细胞谱系分化,揭示了免疫系统的适应性免疫成分在体内调节先天性免疫细胞骨髓生成的新机制。