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. 2017 Mar 8;7:43838. doi: 10.1038/srep43838

Figure 2. Nucleic acid polymers (NAPs) were efficiently taken up by different liver cell types.

Figure 2

The identity of primary human hepatocytes (PHH) (A), Kupffer cells (KC) (B) and liver sinusoidal endothelial cells (LSEC) (C) was assessed by immunofluorescent staining of cell type-specific markers albumin (A), CD68 (B) and LYVE-1 (C) (green), respectively. Nuclei were counterstained with DAPI (blue). Uptake of NAPs was visualized using Cy3-labeld (red) REP 2055 [0.01 μM], REP 2139 [0.05 μM] and REP 2165 [0.05 μM]. Immunofluorescence staining was detected with a laser scanning microscope (LSM; Axiovert 100 M; Zeiss, Jena, Germany) at 20 × magnification. Image analysis was performed with LSM Image Browser (Zeiss). Scale bar 50 μm.