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. 2018 Apr 11;154(4):683–694. doi: 10.1111/imm.12923

Figure 4.

Figure 4

Increased salt intake influences peritoneal macrophage cellularity and their effector functions. (a) Mice were exposed to standard drinking water or 1% NaCl in water for 3 weeks prior to peritoneal lavage. Absolute cell numbers of peritoneal macrophages (F4/80+/CD11b+), 3 weeks after salt exposure. (b) Naïve peritoneal cells were stimulated with lipopolysaccharide (LPS) in the absence or presence of external 40 mm NaCl for 20 hr (n = 6). The frequency of live CD11b+ cells was assessed by flow cytometry. (c) Cytokine production profile produced by cells described in (b). Cytokine levels are represented as units per frequency of live CD11b+ cells. Data show mean ± SEM, and are representative of two independent experiments with similar numbers of mice. A Mann–Whitney U‐test was used, and data were considered significant when P < 0·05 for a 95% confidence interval. *P < 0·05, **P < 0·01, ***P < 0·001.