Figure 4.
Figure 4. Histochemical and immunohistochemical analysis of murine cardiac tissue after LPS administration. H&E staining of WT (A) and EPCRδ/δ (D) mouse heart sections 6 hours after LPS administration. (B,E) Anti-CD45 immunostaining of serial heart sections of WT and EPCRδ/δ mice, respectively, 6 hours after LPS administration. (C,F) Antineutrophil protein immunostaining of serial heart sections of WT and EPCRδ/δ mice, respectively, 6 hours after LPS administration. (G-L) Similar H&E (G,J), anti-CD45 (H,K), and antineutrophil protein (I,L) staining and immunostaining of WT and EPCRδ/δ mice, respectively, at 24 hours after LPS treatment. A Nikon Eclipse E600 light microscope (Nikon, Melville, NY) with a Nikon Plan Fluor objective (magnification, × 20; numerical aperture, 0.5). Images were captured with a SPOT 2 slider (model 1.4.0) camera (Diagnostic Instruments, Sterling Heights, MI) using SPOT software. The images were transferred to Adobe Photoshop 7.0 (Adobe, San Jose, CA) for final reproduction.

Histochemical and immunohistochemical analysis of murine cardiac tissue after LPS administration. H&E staining of WT (A) and EPCRδ/δ (D) mouse heart sections 6 hours after LPS administration. (B,E) Anti-CD45 immunostaining of serial heart sections of WT and EPCRδ/δ mice, respectively, 6 hours after LPS administration. (C,F) Antineutrophil protein immunostaining of serial heart sections of WT and EPCRδ/δ mice, respectively, 6 hours after LPS administration. (G-L) Similar H&E (G,J), anti-CD45 (H,K), and antineutrophil protein (I,L) staining and immunostaining of WT and EPCRδ/δ mice, respectively, at 24 hours after LPS treatment. A Nikon Eclipse E600 light microscope (Nikon, Melville, NY) with a Nikon Plan Fluor objective (magnification, × 20; numerical aperture, 0.5). Images were captured with a SPOT 2 slider (model 1.4.0) camera (Diagnostic Instruments, Sterling Heights, MI) using SPOT software. The images were transferred to Adobe Photoshop 7.0 (Adobe, San Jose, CA) for final reproduction.

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