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. 2011 Dec 16;49(4):357–364. doi: 10.3347/kjp.2011.49.4.357

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© 2011, Korean Society for Parasitology

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 4 — Infection of murine macrophages with GFP-L. amazonensis. (A) Number of amastigotes per macrophage and % of infected macrophages after infection with GFP-promastigotes. (B) The fluorescence signal of noninfected macrophages (control) and infected macrophages. Fluorescence is reported in arbitrary fluorescence units. (C) Microscopic images of infected macrophages. Fluorescence image (C1); Phase contrast image (C2) and Giemsa stained image (C3). Magnification 400×. (D) Flow cytometry of noninfected macrophages (D1) and infected macrophages (D2).