Cheng Pingyan, Corzo Cesar A, Luetteke Noreen, Yu Bin, Nagaraj Srinivas, Bui Marylin M, Ortiz Myrna, Nacken Wolfgang, Sorg Clemens, Vogl Thomas, Roth Johannes, Gabrilovich Dmitry I
H. Lee Moffitt Cancer Center, University of South Florida, Tampa, FL 33612, USA.
J Exp Med. 2008 Sep 29;205(10):2235-49. doi: 10.1084/jem.20080132. Epub 2008 Sep 22.
Accumulation of myeloid-derived suppressor cells (MDSCs) associated with inhibition of dendritic cell (DC) differentiation is one of the major immunological abnormalities in cancer and leads to suppression of antitumor immune responses. The molecular mechanism of this phenomenon remains unclear. We report here that STAT3-inducible up-regulation of the myeloid-related protein S100A9 enhances MDSC production in cancer. Mice lacking this protein mounted potent antitumor immune responses and rejected implanted tumors. This effect was reversed by administration of wild-type MDSCs from tumor-bearing mice to S100A9-null mice. Overexpression of S100A9 in cultured embryonic stem cells or transgenic mice inhibited the differentiation of DCs and macrophages and induced accumulation of MDSCs. This study demonstrates that tumor-induced up-regulation of S100A9 protein is critically important for accumulation of MDSCs and reveals a novel molecular mechanism of immunological abnormalities in cancer.
与树突状细胞(DC)分化受抑制相关的髓源性抑制细胞(MDSC)积累是癌症中主要的免疫异常之一,并导致抗肿瘤免疫反应受到抑制。这一现象的分子机制仍不清楚。我们在此报告,STAT3诱导的髓系相关蛋白S100A9上调增强了癌症中MDSC的产生。缺乏该蛋白的小鼠产生了强大的抗肿瘤免疫反应并排斥植入的肿瘤。将荷瘤小鼠的野生型MDSC给予S100A9基因敲除小鼠可逆转这种效应。在培养的胚胎干细胞或转基因小鼠中过表达S100A9可抑制DC和巨噬细胞的分化,并诱导MDSC的积累。这项研究表明,肿瘤诱导的S100A9蛋白上调对于MDSC的积累至关重要,并揭示了癌症中免疫异常的一种新分子机制。