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Co-stimulation with β-glucans and LPS elicits robust neutrophilic inflammation.

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posted on 2015-08-11, 03:41 authored by Sabelo Hadebe, Frank Kirstein, Kaat Fierens, Kong Chen, Rebecca A. Drummond, Simon Vautier, Sara Sajaniemi, Graeme Murray, David L. Williams, Pierre Redelinghuys, Todd A. Reinhart, Beth A. Fallert Junecko, Jay K. Kolls, Bart N. Lambrecht, Frank Brombacher, Gordon D. Brown

(A) Timeline for challenge with β-glucans (1x107 particles), LPS (100 ng), the combination of both agonists, or PBS alone. (B) Total leukocytes, neutrophils (Gr-1hi CD11bhiF4/80lo), eosinophils (Siglec-FhiGr-1loCD11clo), inflammatory macrophage/monocytes (F4/80hiCD11bhiGr-1lo) and T cells (CD3hiCD4hi) in the BALF of C57BL/6 mice following challenge with the various agonists, as indicated. (C) H&E stained lung sections from wild type (wt), Dectin-1-/- or TLR-4-/- mice challenged with PBS or the combination of β-glucan and LPS. Scale bars represent 50 μm. (D) Cytokine levels in the BALF following challenge, as indicated. *p<0.05, n.s., not significant. Shown are the mean ± SEM of pooled data from at least 2 independent experiments (n = 8–10 mice/group).

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