Owen Jennifer L, Lopez Diana M, Grosso Joseph F, Guthrie Kathleen M, Herbert Lynn M, Torroella-Kouri Marta, Iragavarapu-Charyulu Vijaya
Department of Biomedical Sciences, Charles E. Schmidt College of Science, Florida Atlantic University, 777 Glades Road, P.O. Box 3091, Boca Raton, FL 33431-0991, USA.
Cell Immunol. 2005 Jun;235(2):122-35. doi: 10.1016/j.cellimm.2005.08.032. Epub 2005 Oct 21.
Tumor-associated chemokines, including CC chemokine ligand 2/monocyte chemoattractant protein-1 (CCL2), are thought to play many roles in cancer progression. Here we demonstrate the novel finding that during growth of the D1-7,12-dimethylbenzanthracene-3 mammary tumor in BALB/c mice, there is a dramatic up-regulation of CCL2 in splenic T cells at both the mRNA and protein levels upon stimulation. Of particular relevance is the finding that tumor-infiltrating T cells also produce high levels of CCL2. While a variety of tumor cell lines have been found to produce CCL2, we found no detectable levels of CCL2 protein in supernatants of the cultured mammary tumor cells. Investigation of the mechanisms involved in CCL2 induction showed that treatment of splenic T cells with the tumor-derived factors GM-CSF and phosphatidyl serine (PS) resulted in increased CCL2 production. This increased production may be involved in the downregulation of IFN-gamma by the T cells of tumor-bearing mice previously reported in this model, as treatment of splenic T lymphocytes with CCL2 resulted in a decreased secretion of IFN-gamma by those cells.
肿瘤相关趋化因子,包括CC趋化因子配体2/单核细胞趋化蛋白-1(CCL2),被认为在癌症进展中发挥多种作用。在此,我们展示了一项新发现:在BALB/c小鼠的7,12-二甲基苯并[a]蒽诱导的D1乳腺肿瘤生长过程中,刺激后脾T细胞中CCL2在mRNA和蛋白质水平均显著上调。特别相关的是,肿瘤浸润T细胞也产生高水平的CCL2这一发现。虽然已发现多种肿瘤细胞系可产生CCL2,但我们在培养的乳腺肿瘤细胞上清液中未检测到CCL2蛋白水平。对CCL2诱导机制的研究表明,用肿瘤衍生因子粒细胞-巨噬细胞集落刺激因子(GM-CSF)和磷脂酰丝氨酸(PS)处理脾T细胞会导致CCL2产生增加。这种增加的产生可能与先前在该模型中报道的荷瘤小鼠T细胞对γ干扰素(IFN-γ)的下调有关,因为用CCL2处理脾T淋巴细胞会导致这些细胞分泌的IFN-γ减少。