CCL5, CCR1 and CCR5 in murine glioblastoma: Immune cell infiltration and survival rates are not dependent on individual expression of either CCR1 or CCR5
Copyright policy )CCL5, CCR1 and CCR5 in murine glioblastoma: Immune cell infiltration and survival rates are not dependent on individual expression of either CCR1 or CCR5
Glioblastoma multiforme (GBM) is the most malignant brain tumor. Microglia/macrophages are found within human GBM where they likely promote tumor progression. We report that CCL5, CCR1, and CCR5 are expressed in glioblastoma. Individual deletion of CCR1 or CCR5 had little to no effect on survival of tumor bearing mice, or numbers of glioblastoma-infiltrated microglia/macrophages or lymphocytes. CCL5 promoted in vitro migration of wild type, CCR1- or CCR5-deficient microglia/macrophages that was blocked by the dual CCR1/CCR5 antagonist, Met-CCL5. These data suggest that CCL5 functions within the glioblastoma microenvironment through CCR1 and CCR5 in a redundant manner.
- University of Florida United States
- University of Florida United States
- University of Florida
Receptors, CCR5, Brain Neoplasms, Cell Survival, Macrophages, GL261, Receptors, CCR1, Met-CCL5, RANTES, Mice, Gene Expression Regulation, Cell Movement, Animals, Humans, Microglia, Glioblastoma, Chemokine CCL5
Receptors, CCR5, Brain Neoplasms, Cell Survival, Macrophages, GL261, Receptors, CCR1, Met-CCL5, RANTES, Mice, Gene Expression Regulation, Cell Movement, Animals, Humans, Microglia, Glioblastoma, Chemokine CCL5
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