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. 2018 Sep 26;9:2190. doi: 10.3389/fimmu.2018.02190

Figure 1.

Figure 1

Comparison of Galectin-1 expression in immune cells. Gal-1 is detected by western blot in purified immune subpopulations. T lymphocytes were purified from lymph nodes, antigen-presenting cells from spleens. The specificity of the technique was verified using Lgals1-/- cells. Additionally, Gal-1 levels in TRAMP-C1 cells are comparatively shown. 20 μg of protein was resolved on 15% SDS-PAGE and blotted with commercial anti-Gal-1 antibodies. (A) Representative immunoblot (n = 3). (B) Mean Gal-1 levels in the three independent experiments. The results are expressed as Gal-1/β-actin ratio. (C,D) Immunosuppressive effect of endogenous Gal-1 expression in TRAMP-C1 tumor cells and in lymphocytes. Lymphocytes harvested from wild type (C) or Lgals1-/- (D) mice were polyclonaly activated in presence of 10% wild type APC and 1% of control or modified TRAMP-C1 tumor cells. Proliferation was measured at 72 h by CFSE dilution. Black line: TRAMP-C1 cells with downregulated Gal-1 (stable transduced, 90% of Gal-1 down-regulation-data not shown-). Gray line: TRAMP-C1 cells transduced with a control lentivirus. Representative of two independent experiences.