Figure 4
Figure 4. Immunoelectron microscopy analysis of pDCs during activation by flu. Ultrathin cryosections from pDCs exposed for 0, 3, or 24 hours to flu were prepared. Sections were then labeled using 10-nm and 15-nm immunogold particles for MHC II and LAMP-1 molecules, respectively. The 3 large sections of pDC presented (time 0, 3, and 24 hours) are electron microscopy images, which have been obtained using the Multiple Image Alignment function of the iTEM software (Eloïse; Electron Optics Instrument Service, West Orange, NJ). The 2 images on the bottom right show enlargements of typical MHC II+ compartments after 24 hours of flu exposure.

Immunoelectron microscopy analysis of pDCs during activation by flu. Ultrathin cryosections from pDCs exposed for 0, 3, or 24 hours to flu were prepared. Sections were then labeled using 10-nm and 15-nm immunogold particles for MHC II and LAMP-1 molecules, respectively. The 3 large sections of pDC presented (time 0, 3, and 24 hours) are electron microscopy images, which have been obtained using the Multiple Image Alignment function of the iTEM software (Eloïse; Electron Optics Instrument Service, West Orange, NJ). The 2 images on the bottom right show enlargements of typical MHC II+ compartments after 24 hours of flu exposure.

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