The expression of CCL2 by T lymphocytes of mammary tumor bearers: Role of tumor-derived factors

被引:24
作者
Owen, JL
Lopez, DM
Grosso, JF
Guthrie, KM
Herbert, LM
Torroella-Kouri, M
Iragavarapu-Charyulu, V
机构
[1] Florida Atlantic Univ, Dept Biomed Sci, Charles E Schmidt Coll Sci, Boca Raton, FL 33431 USA
[2] Univ Miami, Sch Med, Dept Microbiol & Immunol, Miami, FL 33136 USA
[3] Sylvester Canc Ctr, Miami, FL 33136 USA
[4] Johns Hopkins Univ, Sch Med, Sidney Kimmel Canc Ctr, Baltimore, MD 21231 USA
关键词
chemokines; mammary tumor; T lymphocytes; CCL2; GM-CSF; IFN-gamma; PS;
D O I
10.1016/j.cellimm.2005.08.032
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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-in filtrating 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. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:122 / 135
页数:14
相关论文
共 58 条
[1]  
Ajuebor MN, 1999, J IMMUNOL, V162, P1685
[2]  
ALAOUKATY A, 1994, BLOOD, V83, P1299
[3]   INDUCTION OF NATURAL-KILLER-CELL MIGRATION BY MONOCYTE CHEMOTACTIC PROTEIN-1, PROTEIN-2 AND PROTEIN-3 [J].
ALLAVENA, P ;
BIANCHI, G ;
ZHOU, D ;
VANDAMME, J ;
JILEK, P ;
SOZZANI, S ;
MANTOVANI, A .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (12) :3233-3236
[4]  
Amann B, 1998, BRIT J UROL, V82, P118
[5]   Inhibitory effects of negatively charged liposomes on nitric oxide production from macrophages stimulated by LPS [J].
Aramaki, Y ;
Nitta, F ;
Matsuno, R ;
Morimura, Y ;
Tsuchiya, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 220 (01) :1-6
[6]   Interleukin-6 induces monocyte chemotactic protein-1 in peripheral blood mononuclear cells and in the U937 cell line [J].
Biswas, P ;
Delfanti, F ;
Bernasconi, S ;
Mengozzi, M ;
Cota, M ;
Polentarutti, N ;
Mantovani, A ;
Lazzarin, A ;
Sozzani, S ;
Poli, G .
BLOOD, 1998, 91 (01) :258-265
[7]   Cellular responses to interferon-gamma [J].
Boehm, U ;
Klamp, T ;
Groot, M ;
Howard, JC .
ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 :749-795
[8]   Selective suppression of IL-12 production by chemoattractants [J].
Braun, MC ;
Lahey, E ;
Kelsall, BL .
JOURNAL OF IMMUNOLOGY, 2000, 164 (06) :3009-3017
[9]   LYMPHORETICULAR CELLS ISOLATED BY CENTRIFUGAL ELUTRIATION FROM A MAMMARY ADENOCARCINOMA .1. CHARACTERIZATION OF AN INSITU LYMPHOCYTE SUPPRESSOR POPULATION BY SURFACE-MARKERS AND FUNCTIONAL REACTIVITY [J].
BUESSOW, SC ;
PAUL, RD ;
MILLER, AM ;
LOPEZ, DM .
INTERNATIONAL JOURNAL OF CANCER, 1984, 33 (01) :79-85
[10]   ISOLATION OF A NITRIC-OXIDE INHIBITOR FROM MAMMARY-TUMOR CELLS AND ITS CHARACTERIZATION AS PHOSPHATIDYL SERINE [J].
CALDERON, C ;
HUANG, ZH ;
GAGE, DA ;
SOTOMAYOR, EM ;
LOPEZ, DM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :945-958