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. Author manuscript; available in PMC: 2015 Apr 1.
Published in final edited form as: Neuropathology. 2014 Apr 7;34(5):429–437. doi: 10.1111/neup.12121

Fig. 3.

Fig. 3

Double label immunocytochemistry for enterovirus (red) (A) and synaptophysin (green) (B) demonstrate infection of individual cells in the islets of Langerhans shown in the merged image (C). Double-label immunocytochemistry of spleen for CD21 (red) (D) and enterovirus (green) (E) demonstrated co-localization within follicles shown in the merged image (F). In situ hybridization with sense and anti-sense probes demonstrates that spleen signal was limited to detecting entrapped virion without detecting infected cells (see results). Double-label immunocytochemistry for microtubule-associated protein 2 (MAP2) (green) (G) and in situ hybridization for coxsackie B virus (CB4) (black grains) (H) demonstrates infection of cortical neurons shown in the merged image (I).A–F bar = 20 μm, G–I bar = 50 μm.