Fig. 5.
Fig. 5. Model of DC differentiation in the mouse spleen. / (1) Access of CD8α− DCs to the marginal zone either from the blood via the marginal sinus (a) or by intrasplenic differentiation from an unknown precursor (b). (2) Transient retention of CD8α− DCs in the marginal zone reticular meshwork. (3) Reversal of CD8α− DC retention in the marginal zone. (4) Migration of CD8α− DCs to the inner white pulp accompanied by the acquisition of the phenotypic and functional features of CD8α+ DCs. Finally, CD8α+ DCs die in situ or leave the spleen via lymph vessels (see “Discussion” for a detailed explanation). Principal changes accompanying the proposed maturation of CD8α− DCs into CD8α+ DCs are indicated. IFN-γ indicates interferon γ.

Model of DC differentiation in the mouse spleen.

(1) Access of CD8α DCs to the marginal zone either from the blood via the marginal sinus (a) or by intrasplenic differentiation from an unknown precursor (b). (2) Transient retention of CD8α DCs in the marginal zone reticular meshwork. (3) Reversal of CD8α DC retention in the marginal zone. (4) Migration of CD8α DCs to the inner white pulp accompanied by the acquisition of the phenotypic and functional features of CD8α+ DCs. Finally, CD8α+ DCs die in situ or leave the spleen via lymph vessels (see “Discussion” for a detailed explanation). Principal changes accompanying the proposed maturation of CD8α DCs into CD8α+ DCs are indicated. IFN-γ indicates interferon γ.

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