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tel-00827710, version 1 - 29 May 2013<br />

1) Presentation of intracellular antigen on MHC-I molecules<br />

MHC-I molecules are expressed by all nucleated cells and allow for the presentation of<br />

intracellularly synth<strong>et</strong>ized pepti<strong>de</strong>s on their surface. Basically, endogenously synth<strong>et</strong>ized<br />

proteins are <strong>de</strong>gra<strong>de</strong>d by the proteasome or the immunoproteasome in the cytosol and<br />

transferred into the endoplasmic r<strong>et</strong>iculum (ER) through the TAP transporter (Buckwalter and<br />

Albert, 2009). They are then loa<strong>de</strong>d on MHC-I molecules, which transit through the Golgi<br />

complex to reach the cell surface (Figure 2, pathway 1, red arrows).<br />

Figure 2. Generation of MHC-I-pepti<strong>de</strong> complexes from endogenous and exogenous antigen. The<br />

pathway 1 (red arrows) corresponds to the direct presentation of endogenously synth<strong>et</strong>ized pepti<strong>de</strong>s.<br />

The pathway 2 (blue arrow) represents the cross-presentation of exogenous antigens. Figure from<br />

Buckwalter <strong>et</strong> al., 2009.<br />

2) Presentation of extracellular antigens<br />

In or<strong>de</strong>r to be presented, extracellular antigens must first be taken up from the outsi<strong>de</strong><br />

environment by the APC. Different endocytosis pathways will be used for this process,<br />

<strong>de</strong>pending on the nature of antigen of interest. Particulate antigens, such as cell-associated<br />

antigen, are taken up by phagocytosis whereas receptor-mediated endocytosis or pinocytosis<br />

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