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

Table 4. Mouse DC subs<strong>et</strong>s. Mono-DC, Monocyte-<strong>de</strong>rived DC; LC, Langherans cell. (*) This subs<strong>et</strong><br />

was shown to respond to poly I:C but TLR3 was not i<strong>de</strong>ntified in these cells.<br />

2) Specialization<br />

(a) Ability to present antigen<br />

The different cDC subs<strong>et</strong>s have been <strong>de</strong>scribed to have various abilities for antigen uptake<br />

and presentation. The CD8α + DCs showed a superior capacity to take up dying cells (Iyoda <strong>et</strong><br />

al., 2002), which is correlated with their relatively increased expression of some receptors<br />

known for clearance of <strong>de</strong>ad cells, such as Clec9A. Moreover this subs<strong>et</strong> has been<br />

<strong>de</strong>monstrated to b<strong>et</strong>ter cross-present antigen compared to the CD8α - DC subs<strong>et</strong> from the<br />

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